Gluten Intolerance)

2007-01-31 20:35:05

Thanks for the input Rachel. The diet I have been on since June of
this year limits wheat anyway but I have a friend with lots of lupus
running in her family and they all find that with no wheat products
they are much better. So I eliminated almost all wheat and the only
grain I usually have is Millet (which is the only "alkaline" grain).
SO far it hasn't helped, but I will keep on trying!!! (I think millet
is gluten free but am not sure).
I'll check out the archives too as soon as I get a chance.
-Chris(tine)(I added that so you would know I am a female Chris...-)

question about muscle aches

2007-01-31 20:00:45

Dear Alice...
Oh boy, do I ever... It seems normal to try and compensate for pain in certain
areas by moving strangely and causing muscle pain in other areas. It also seems
that when an area is really inflammed the muscule becomes so also...
It's so hard sometimes to know why something is hurting... Does anyone else
face this battle? I mean, I know I have PA ~ and I know which joints it tends
to impact, but then I feel a pain here or there and I start to worry that it is
spreading. Then I wonder if I "did" something to cause the pain, or is it just
"getting older" pain, or...
Anyway, I have become so focused on "pain" that I think I notice too much... Of
course, I am one of the luckier PA'ers ~ I have only had two major flares over
the last 19 years ~ bookending the time period, but I'm always achy... After
taking Remicade, Mtx and doing acupuncture, I'm hoping (praying, crossing
everything and knocking on all the wood I can find) that I am heading back into
remission again...
Best Wishes,
Karen (idaho)

Re: I'm new to this ..Re to Fran--jaw...

2007-01-31 15:09:42

Hi Fran, I am thrilled to have found this group AND this time around
I got a lot of replies!!! I'll answer them all until my hands cry
uncle!! My dream would be a new PC with a great speech recognition
program so I could keep in touch with people w/o wearing out those
fingers, MCPs, and wrists!
I had it bad in one side of my jaw for several months, back in the
beginning when it seems every week my body added a new joint into the
pain party. :(
Somehow eventually the jaw stopped hurting, now it just has a
tremendous amount of crepitus(Sp??) and makes a lot of creaking every
time I yawn!! I hope and pray that yours makes a remission soon!
Also, the diet I am following suggest no tomotoes, eggplants
("nightshade" family), so i have been avoiding those.
-Chris(tine)

Scientists Find A Key To Immune System's Ability To Remember

2007-01-31 08:41:04

Scientists Find A Key To Immune System's Ability To Remember
http://www.sciencedaily.com/releases/2006/10/061023193624.htm

Re: I'm new to this ...(Re Elaine's reply)

2007-01-30 23:44:00

Hi Elaine, thanks for posting! I think the name of the author is
Pagano. I heard about it at a graduation party for my sons' roommate
some lady approached me and asked what was wrong with me(I use hand
splints and a special cane with an arm rest since my hands/wrists can
use a regular cane - so I look like the walking wounded!!). I told
her I had RA (I often say that because otherwise people have no idea
what PA is!!!). She has a daughter who had P since she was a child
and was recently living for several months in Germany and she
developed a bad case of PA, she went to a chiropractor who told her
is was probably due to the 'rich' German food and told her about this
book. She started following the diet and in about 3 - 4 wks she was
much much better. I was amazed so i got on Amazon and found the book.
My 3-4 wks have come and gone and still no relief but getting the
weight off is wonderful!!! ALSO PEOPLE have been telling me I look
younger and have a "glow" about my face. Having just turned 50 that
is nice to hear!!!! LOL!!!! They say just getting 10 or 15 pounds off
relieves our knees tremendously so I'll keep working on it!
Take care and be as well as you can be.
-Chris(tine)

RE: [PsoriaticArthritis] any thoughts please!

2007-01-30 13:38:44

Dear Leanne, I can understand your frustration. There isn't anything worse
than the doctor telling you nothing can really be done about your problem.
Especially when your problem is huge and causing so much pain with someone
you love. I think she is wrong that PA doesn't respond to anything. I
haven't been a huge success story, but so many other members have been.
I also think that pain killers can really help you deal with PA. I don't
know how I would make it without them. I know everyone worries about
addiction and my own daughter has a serious case of fibromyalgia and has to
take pain medication. It gets to the point, where she could either spend
her life in bed in pain, or take medication and have a somewhat normal life.
Without her medication I know she would never make it to her college classes
or be able to live on her own. She wouldn't be able to function since the
pain is so severe at times. I watch her from time to time to see if I ever
think she is abusing medication and if anything she waits too long to take
her pain medication. I really do believe too many people worry about
narcotic addiction, when they could relieve their pain and enjoy life more.
It's obvious that some people have problems with narcotics, but most of the
time I don't think they have true pain like we do. The current research
shows that very few people in pain become addicted to their medication.
Though I know how it is to be a mother and worry about that too.
Prednisone does help with the pain and swelling. The problem of course is
the side effects. Hopefully if Owen has to take it, you can keep it on a
low dose for a short period of time. I've had more problems getting off
prednisone than any of my pain mediations. The side effects are miserable
too, but I've been on it now for over 3 years. So far I can't seem to get
much lower than 12mg without going into a major flare.
I wish I had some comforting words to give you on Owen and take away his
pain. All I know is the future is brighter with the new drugs on the
market. Hopefully, he'll respond to one of them and get back his life. Hang
in there and my thoughts are with you. Take care of yourself and don't get
too down over all of this. Much easier to say than to do, I know. Love,
Fran

Current med list

2007-01-30 06:11:52

I'll play along, my current meds are:
Altace (hypertension)
Ambien (sleep)
Azulfidine (arthritis)
Carafate (reflux)
Humira (arthritis)
IB-600 (inflammation & pain)
Nexium (reflux)
TriClor (to reduce high triglycerides)
Ultracet (pain)
Zyrtec (allergies)
My favorite stress reliever is cheesecake :)
Warm blessings, Jane

FEELING MAD!

2007-01-30 04:18:47

Fran, thanks for putting my thoughts into words. I
agree with you 100%. Jane

Re: I'm new to this ...(Re liver cleansing diet)

2007-01-29 22:14:25

Thanks for replying!!! One reason I had to stop MTX and Arava was my
liver enzymes went beserk so I think it is good to be on this diet
which is also supposed to help the liver. I will try to find the book
you suggest also, it will be interesting to compare the two diets!
We sure put alot of poison medicines into ourselves don't we!!!
I hope the biologics get approved in your country soon!!!
As for overweight, I even had a VP at my former employer tell me all
about someone he knew who supposedly had RA and lost a few pounds and
was all healed. SIGH!!! Well, I have now lost a total of 66 pounds
and I am not healed yet!!! (I still have some more to lose, but at
this point I give up thinking it will cure me but if it takes some
pressure off my tender knees, ankles, MTPs and sausage toes I will be
happy for that I guess!)
And it does keep the relatives from making too many "maybe if you
tried losing weight" comments when they see me already losing it!!!
Take care!
Chris(tine)

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Re: I'm new to this...(Re Ronnie--Enbrel)...

2007-01-29 07:30:39

Hi Ronnie, Thanks for the post. I can't use enbrel since I had a bad
side effect from Remicade and the neurologist says I can't use any
more "anti-TNF" medicines. :( Remicade was sort of a miracle for me
at first. After my first infusion all my swellings went w/in 48 hrs!!
But then after a few months it seemed to not work as well, the
Remicade sales person told my doctor that they had new guidelines and
my dosage could be safely increased. Well, guess what? It seems to
have been the increased dosage that gave me the problem! (Some kind
of nerve damage that resulted in neuropathy...like I needed ANOTHER
problem---isn't psoriasis and arthrits enough??? -)
I heard there is a new med supposedly going to be approved mid-2005
here in the USA which is NOT an "anti-TNF", so I've got my hopes
pinned on that since this diet is helping me look better and lose
weight but isn't helping the old joints or scratchy P.
Take care,
Chris(tine)

Re: Venting..

2007-01-29 07:03:17

That's awful. That's about as low.... take care Heather. Thanks
for sharing it with us.
Karen

P.S. Can't open my hotmail

2007-01-28 21:20:36

thanks Jean!

Re: [PsoriaticArthritis] PA and Acupuncture

2007-01-28 11:24:16

In a message dated 11/4/2004 6:08:10 AM Eastern Standard Time,
wodell3320@... writes:
Just curious.......has anybody ever tried acupuncture for this
lovely disease called Psoriatic Arthritis?
I did go for a few sessions of accupuncture and did not find it helpful. I
don't know if anyone else here had tried it. For me, I go for weekly
massages in my chiropractors office and that is helping me. I don't know if it
helps the fibro or the PA but it makes me feel better.
Janet

the cause of RA

2007-01-28 05:56:26

I learned that these rheumatic diseases were recessive, meaning that you had to
inherit from each parent.
I am adopted but I know on my biological mother's side there are no rheumatic
conditions.
The problem for me developed when I was under prolonged severe stress.
Remember that years ago scientists believed that rheumatic diseases were caused
by viral or bacterial infections. With the discovery of prednisone, they
thought the cure was found. Of course, they eventually found out that
prednisone was quite destructive but that is when research went on the auto
immune track.
HTH
Denise
Pray the Rosary
www.Jmichaelstyle.com

Dress Shoes

2007-01-27 22:20:38

Hi
I have found dress shoes that work, although they are flat.
I buy Monroe brand. The insole comes out and your orthotic goes in. I have
had good luck with every one of the shoes I buy in this brand. They all have
the same base but all different kinds of tops.
Barb

age

2007-01-27 19:51:01

Jerre-54 years old, diagonosed 18 months ago, whole body tendonitis and
bursitis, no p,
oa in my basal joints and neck. How long I have had it? I've had bouts of
tendonitis and
busitis on and for 40 years but blamed it on spending 20-25 hours a week Doing
gymnastics and abusing my body. At 49 my previous md said the pain was just
because I
was getting old and I would have to live with it! She got mad when I told her a
friend (also
her patient) had recommended I see my current rhuemy. Thank goodness for once I
didn't
listen to Authority!
jerre

Heading to Enbrel...scared/excited/relieved/etc...

2007-01-27 14:10:09

Hi everyone. Well, my flare up is lessening some. I mean, I can use
all of my fingers, and can move and stay awake now during the day, so
to me that is an improvement! (hahaha) Anyway, I saw my reheumy
today. She said that she wants to start me on Enbrel. I am sooo
excited, because it seems to have good results, but I know it can
also be a nightmare.
So I was all pumped...ready to get the paperwork rolling through my
perscription company....but, when I went back, the pharm said they
covered it! BUT my copay might be a little more than I am used to.
Well, for 4 weeks of 2 injections a week, they wanted $245!!! I
about died. So, I said I needed to think that one over... so I
decided somehow I would make extra money...and do it anyway...well, I
just happened to think about my home delivery service..and so I put
it in, expecting to find nothing better...BUT, they will cover 12
vials for $30!!!!! It may be a little more or less depending on how
they will disperse it...but OMG!!! I want to cry right now!
So now I am all excited for the cost, but scared to death of the drug
and the injections and what I am doing to my body! I mean, doesnt it
scare you sometimes, thinking how we are completely messing with our
body's physiology? I mean, I know ours IS messed up, but we are
taking pills/injecting ourselves with stuff that is completely
changing the exact body we were given? I mean, I think medicine is
fantastic...but it can also be soooo scary!
Sooo, hopefully, I will be starting by the end of 3 weeks...they have
classes here every few weeks...so once I get through that, I should
be all set...I have no idea what I am in for...I am going to look up
archives and such...
I bought some nice elbow wraps today, and they are nice..they keep my
elbow warm, are adjustable, and keep the joint nice and tight. I
feel great with them on...I figure I wil just buy them for all joints
in my body...i might look funny, but eventually, I will feel OK!!!
Hugs everyone...
Dawn

Re: tazarotene

2007-01-27 10:25:05

Welcome Lakethundermom,
I'm sorry for what you are going through right now but very glad you
have found this board. You will make many new friends here and as
well, glean much helpful information in dealing with this disease.
WE are all in it together and really hold each other up,
emotionally. It may not take away the pain, but it's certainly
wonderful to not feel alone with it anymore.
Take care,
Karen

Re: I'm new to this ...(Re SusieSue)

2007-01-27 09:43:15

Thanks for the reply, This time I got a lot of them!!
With all your problems it was really sweet of you to reply. I hope
you can find some relief soon.
I'm thinking of getting a more powerful PC and speech recognition
software so I can stay in touch w/o killing my fingers. If I ever do
it I'll post here with what I get so others will know what works.
Take care!!
Chris(tine) (from Vermont originally but living in California now)

RE: [PsoriaticArthritis]Janet and muscle pain

2007-01-26 16:58:51

RE:
Do you and your daughter get horrible muscle spasm all over from the
fibro. I can turn in a certain position and get spasms in my back and all
over the abdominal muscles.
Janet
Dear Janet,
You described a typical day for my daughter and myself as much as I hate to
admit it. It doesn't take anything to stress out a muscle or cause a bad
spasm that seems to last for days. At times it feels like a spot is on
fire, or like someone is simply stabbing you with an ice pick. (Best way to
describe the pain...) My daughter gets horrible shoulder pain and neck
spasms from simply driving, and it can be for a short time, like only 20
minutes. We carry pillows with us in the car to support our arms when we
drive or even ride as a passenger. I know with Fibro there is a triangle
area outside the body that is considered high pain areas. For example if
you keep your arms away from your body for any length of time, you will have
a spasm. (I wish I could draw you a picture..lol) But it is really true
for me and my arms. For example I have a horrible time holding my hair
dryer, and it's gotten worse since my left hand is numb now. ( I plan to
buy that hair dryer stand everyone was talking about on here and finally
found it in a catalogue I got the other day.) But any movement away from
your body with your arms or your legs can trigger a bad spasm in your
shoulders, back, chest or just about anywhere. One thing I think really
sucks and unfortunately that's the best word I can come up with, is it
hurts my abdominal muscles to even laugh a lot. You know that crazy
laughter where you lose control and can't stop laughing...well if I do that
my stomach muscles go into a major spasm and I think I'm going to do die.
Half the time, I'm not sure if I'm crying from the laugher or from the
pain...lol. It really seems to target any muscle you don't use a lot or do
repetitive motions. I guess that's why exercise can be so important for
fibro. I know I was at my best when I forced myself to work, even though I
might be late to work or had to lie down at work. Going back to bed, even
though it was really tempting and I did give in at times, really never
helps. (Though sometimes a short nap can release a spasm when nothing else
can seem to work.) Now that so many other things have hit me, Fibro is just
one of the problems I deal with, but when it's bad it sure takes over from
everything else.
We both used to take Flexerile and if you take it everyday you do eventually
build up a tolerance to feeling tired the next day. With Zanaflex you don't
have to deal with the morning after feeling, which is nice. When I first
developed fibro I know I was elavil for about 4 years. (That also adds
weight unfortunately) But it does help you sleep as well. I have about 10
pillows I sleep with every night. My husband claims I build a fort around
me every night before I go to sleep. I guess I do actually, but that way I
have more support for my arms, shoulders and even my legs at times. When
it's bad, I go from room to room, bed to chair, trying to find a place that
will help with the pain. I feel like one of my little dogs when they hurt
and they think if they move the pain won't go with them....lol. So some
nights we have real parade around here at night. I'm up walking around at
all hours and my two little dogs are following behind me everywhere I
go...lol. What a life.
I hope some of that helped Janet. I've read I think every book on fibro on
the market, except for maybe anything new in the last 18 months. When my
daughter got it, I felt like so many people had no clue about the disease I
had to learn all I could to educate people and help her anyway I could.
Plus I think it helped me to to feel like I was doing things correctly and
that we had tried all the options there were. I'm lucky in a way that my
fibro isn't as bad as my daughters. She has the worst case I've ever seen.
Not only does she have all the muscle pain, but she has all the strange side
effects that so often go with fibro, like migraines, IBS, dry eyes,
depression and the list goes on. I keep hoping she will go into remission
or at least it will let up some, but so far it's a real struggle for her
everyday to just get out of bed and try to go to class. I admire her
courage for going even when she hurts all over and has to sit in
uncomfortable chairs at school. She thinks about what chair she will have
to sit in where ever she goes, not a normal thing for a 21 year old to be
concerned about.
Well I've written you a book and you only asked one question..lol. Take
care Janet and I hope the spasm let up. Love, Fran PS Sometimes going
from ice to heat on a bad area will stop the spasm too. Just a thought.

Re: Thanks! &amp; PA questions

2007-01-26 16:42:00

d,
I soak my feet in epsom salts or mineral salts this seems to help my
feet. I use an incombent bike that I ordered online, it takes the
pressure off of my spine. Saying no to loved ones is a learning
experience. It takes practice and patience. Their reactions and
perceptions are theirs. I know how much energy I have. I allocate
and prioritize how I will use my energy. When I am asked to do
something and I must say no, I set a boundary and do not allow the
circle of questions, because it wears me out. I say "I am sorry that
I am not able to go to little Jimmey's party today, I will think of
him during his celebration." "I have compassion for your inability to
understand my situation and No one could comprehend this disease
unless they suffered from it." They ususally stop and realize that
they are not helping you by applying pressure. I always try to show
compassion for the people who do not understand. I have nothing to
prove to anyone. It is my war, my challenge and sometimes it is
where my wisdom comes from. Hope this helps.
Carolyn :)

Re: [rheumatic] Brand name versions of minocycline -&gt; prices

2007-01-26 09:38:22

Jeff,
Jeff, I would take my chance with Minocin by Stiefel in Canada. I
spoke with Glen, the pharmacist of RxCareCanada.com, 1-800-381-3594.
He stated that the capsules are Orange and Purple. The contents are
pelleted, the tell-tale sign of brand name Minocin. The capsules are
imprinted with "Lederle M4." Lederle was the original developer of
Minocin, later merged into Wyeth. One hundred 100 mg capsules cost $147.01. See
http://rxcarecanada.com/Minocycline.asp?prodid=2256
RxCareCanada.com also sells generic minocycline, but I did not
inquire as to the manufacturer.
There may be lower cost suppliers of Minocin by Stiefel in Canada.
I am maintaining a web page with feedback from our group on results
with generic minocycline by different manufacturers. I would be
willing to take my chance on TEVA and Watson. Please see
http://www.tmgp.com/generic-mino.htm
Sincerely, Harald

Re: I'm new to this ...(Re Cheri..Blood type system??)

2007-01-26 06:37:19

Hi Cheri,
Thx for the reply. I have not heard about the blood type system.
Where can I find out about it?
I've just turned 50 so I know what you are going through, this
disease makes it feel like old age didn't creep up on us, it makes it
feel like it attacked us!!!
I would suggest if you haven't already done so, find out if your
employer offers a disability insurance package and hopefully you can
sign up during open enrollment with no medical disclosure needed. We
would be in big financial trouble if I hadn't had disability
insurance, as my husband, who is in his 60s already, got laid off
about 2 months before I was Dx'd, and only about 6 months before I
had to stop working!!!!
As for SSDI, I got a lawyer after I got my first denial and with his
help I got it on a review w/o even having to do a formal appeal.
However, the lawyer gets part of your money!!!
Maybe you know all this but if you can afford it, COBRA will cover
you with health insurance until you qual for SSDI at which time you
go on Medicare. And by the time you do, Medicare will have drug
coverage, so that should help.
Good luck!!!
Chris(tine)

Re: [rheumatic] AP Good Progress

2007-01-25 21:43:30

Hi Janie,
Thanks for sharing your progress with us. It's especially helpful for the
newbies to be able to read how others are faring on the AP. I remember how
hard the first couple of years were. I started AP in 1998 and am doing very
well. I would say I'm at least 80% improved from then. Most days I don't
even have to think about having RA. I am very appreciative of that.
Take care,
Ute

Short-term Use of Prednisone

2007-01-25 19:08:22

Esther Warkov,
It is my understanding that taking 10 mg of Prednisone for a couple
of days does not cause a dependency or require weaning. Similarly,
dependency is not caused by a single Cortisone shot.
Long-term use of high dosages of Prednisone, such as 40 mg, causes
the body to stop manufacturing the hormone Cortisol and would
requiring weaning under a doctor's supervision. The typical daily
amount of Cortisone produced by a healthy body is the equivalent of
7.5 mg of Prednisone.
I am currently on 2 mg of Prednisone for PMR. I am now reducing the
dosage by 0.5 mg every 4 weeks.
Sincerely, Harald

Re: New medicine has 'major impact' on psoriasis - beneficial for PA too

2007-01-25 11:14:25

I just found out from the psoriasis clinic in Vancouver that this
medecine, Amevive, is definitely beneficial for PA. I was told that
it is one of the newer biologics (like remicade or enbrel) but only
requires two 12 week courses of injection to last for a whole year.
It is newly approved in Canada for psoriasis, but has been used for
PA for a while. It is supposed to have fewer risks than the other
biologics, as it targets the biological cause of PA and psoriasis
more specifically and doesn't seem to lower the immune response in
the way that remicade & enbrel do (it's been in clinical trials for
10 years, but who knows what problems will be discovered down the
road). The BC pharmacare program doesn't cover the yearly cost,
$14,000, yet. But has recently started approving remicade for PA, so
it is definitely possible Amevive may soon be covered. In the
meanwhile, 3rd party insurers have been covering it for PA and for
moderate to severe psoriasis. I plan to talk more about this with my
rheumatologist.
Meanwhile, I have been having a lot of success with a combo of 100
mgs doxycyline, 25 mgs mobicox and 1.25 grams of prednisone per day
for the PA and dovonex and tacrolimus with oculusion (saran wrap) for
the psoriasis. However I think it would be really nice to have one
simple 12 week treatment to take care of everything for a whole year.
Sharon

Re: [PsoriaticArthritis] Feeling Leperous attn: Fran

2007-01-24 23:49:28

In a message dated 11/10/04 5:19:37 AM Central Standard Time, fran@...
writes:
~~~They [finger nails] have white lines running horizontally and sort
of look like the nail was smashed in a door. They get white lines and spots
all over them, but it seems to be under the nail.~~~ Fran
Hi Fran hard to tell from your description exactly what you mean by "white"
this page may be helpful Fingernails and nutrition Not suggesting this
product but the page has more good infoZinc Deficiencies - Can't Taste Foods?
Stinky
Feet? White Spots on Nails? Orin

Re: [rheumatic] Anyone in Toronto?

2007-01-24 16:43:12

Dr. Keystone at Mount Sinai is very good. I don't think he will do the AP.
Linda

Study of Ultraviolet-A1 Light... may be effective in mitigating Lupus (SLE)

2007-01-24 16:27:44

Experimental Studies are Ongoing but...
1: Lupus. 1996 Aug;5(4):269-74.
Ultraviolet-A1 (340-400 nm) irradiation therapy in systemic lupus
erythematosus.
McGrath H, Martinez-Osuna P, Lee FA.
Department of Medicine, Louisiana State University Medical Center, New
Orleans,
USA.
Ultraviolet-A1 (UV-A1) wavelengths have been found effective in mitigating
signs
and symptoms of disease activity in systemic lupus erythematosus (SLE) but
studies have been uncontrolled. To rigorously assess the effectiveness and
safety of daily low-dose UV-A1 irradiation as a therapeutic agent in this
disorder we enrolled 26 women with SLE in an 18-week two-phase study. During
the
initial six-week prospective, double-blind, placebo-controlled phase, the
patients were divided into two groups; Group A was exposed to 60kJ/m2 of UV-A1
(340-400 nm) irradiation within a sunbed five days a week for three weeks and
Group B was exposed for an equal amount of time to visible light of greater
than
source for three weeks. During the second phase-2 weeks-patients and
physicians
were unblinded and patients were irradiated with progressively decreasing
levels
of UV-A1 only. Twenty-five patients completed the six-week placebo-controlled
phase of the study and eighteen patients participated for the entire 18 weeks.
In Group A the systemic lupus activity measure (SLAM) score improved
significantly after three weeks of five-day-a-week UV-A1 irradiation (P <
0.05),
regressing to baseline during the three weeks of placebo irradiation.
Improvement recurred and progressed with six weeks of three-day-a-week UV-A1
irradiation (P < 0.05). Group B patients responded negligibly to the three
weeks
of visible light, more sharply to UV-A1, and as with Group A, maximally to the
six weeks of three-day-a-week UV-A1 (P < 0.01). With twice- and then
once-weekly
UV-A1 irradiation the SLAM scores worsened slightly. All patients decreased
their drug use. Anti-double-stranded DNA antibodies (anti-dsDNA) decreased
significantly (P < 0.05) and anti-nuclear antibodies non-significantly. Side
effects were negligible. Visible light had no significant effect. In
conclusion,
low-dose UV-A1 irradiation effectively, comfortably, and without apparent
toxicity diminished signs and symptoms of disease activity in SLE.
PMID: 8869897 [PubMed - indexed for MEDLINE]
Related Links
Ultraviolet-A1 irradiation decreases clinical disease activity and
autoantibodies in patients with systemic lupus erythematosus. [Clin Exp
Rheumatol. 1994] PMID:8039279
UVA-1 cold light treatment of SLE: a double blind, placebo controlled
crossover trial. [Ann Rheum Dis. 2001] PMID:11156542
Longterm ultraviolet-A1 irradiation therapy in systemic lupus erythematosus.
[J Rheumatol. 1997] PMID:9195511
Reversal of brain dysfunction with UV-A1 irradiation in a patient with
systemic lupus. [Lupus. 2003] PMID:12873051
Ultraviolet A1 (340-400 nm) irradiation and systemic lupus erythematosus. [J
Investig Dermatol Symp Proc. 1999] PMID:10537014

Re: [PsoriaticArthritis] Martin - Hospital

2007-01-24 09:11:00

Hi Kathy,
Thanks. As soon as I know I will let you know. I could already be in if I'd
wanted. They told me on Monday that there were putting me into hospital and
said the other hospital would contact me within a week or two. Next night at
teatime I received a phone call asking if I would be available to go in the
next day. I just said that it was too short notice and I wouldn't be available
until Monday. So I don't know when they will call now but talk about quick!
Hopefully when I come out I will no longer look like some strange kind of
Leopard.
Hope you are having a good day today,
Martin

RE: [PsoriaticArthritis] New to this list...Hi

2007-01-24 04:18:20

Dear Hanna, You sound a lot like me since your psoriasis isn't bad. I
started out with just a little spot on my arm and it started spreading in
the past 5 years since the PA has hit. I've been told I have polyarthritis
as well.
I've tried a lot of the medications you mentioned and had bad reactions to
almost all of them. Saying that, you have to remember that I'm not the
usual case and a lot of people have been given their life back by Enbrel and
MTX. I still think they are probably our best hope for the future with PA,
but my body simply can't take them.
I was on MTX for about a week and started having trouble with asthma. I've
had asthma for years, but it has gotten worse every time I've tried a new
drug for PA. I also felt like my glands were swelling on MTX, so I stopped
it after a week. Next I tried Enbrel and believe me I had my hopes so high
and wanted this to work so badly. I had almost the same reaction except the
swelling got really bad and I went into congestive heart failure. Up until
that time, I never had a problem with my heart. I had a chest X-ray done
before I went on the Enbrel and then 2 weeks later; the 2nd X-ray showed my
heart was enlarged and going in to congestive heart failure. That was
pretty scary since I was only 47. After waiting about 9 months and being
okayed by a cardiologist, I was told I could try Humira and it shouldn't
bother any heart problem. (They told me I had diastolic dysfunction, which
is a mild form of heart damage that is normally caused by medication, but of
course, no one would blame it on Enbrel. I still suffer from edema and have
to take water pills everyday. That also could be the results of the
prednisone I've been on.) After my cardiologist said it was ok, I tried
Humira. That one almost killed me. My face was swollen so bad and I went
into respiratory failure. I ended up on tons of prednisone to get rid of
the chest inflammation, but it took almost 3 months to get the Humira out of
my system, and I think I only took 4 shots? It was a very small amount.
When I see the commercials on TV for Enbrel and Humira, I want to scream
about the side effects, but I have to remember that I am again in a very
small percentage group.
The good news is I had the guts to try one more medication and this time it
helped me. It is Arava and so far I seem to be ok. I have to say that
Arava has taken away a lot of the exhaustion and fatigue. I still have pain
and still have a lot of bad days, but most of that is from dealing with the
damage to my joints. The main thing is to try the new drugs, but be on the
look out for anything strange and report it to your doctor ASAP. It is a
gamble, but so is life. Luckily most people are fine and you probably will
be too. I don't know if it is connected at all, but I'm allergic to a lot
of things and maybe that makes me more at risk...who knows?
Well good luck and I hope I didn't scare you off. Take care and write me
anytime if you have a question. Love, Fran

FEELING MAD!

2007-01-24 01:35:41

Well written Fran and sound advice. Mo

Re: [rheumatic] JRA?

2007-01-23 17:21:01

I am just home from work and am too tired to deal right now. My 16 year old
daughter was diagnosed with systemic onset JRA when she was 7 1/2. We visited
Dr. Franco in Riverside, CA and she was put on Biaxin. For the moment I
would suggest that you visit the "roadback.org" website for some information on
antibiotic therapy. When I have time, I will email more details. Depending on
the type of JRA you might want to look at diet also.
My daughter's arthritis was very severe with 11 involved joints and high
fevers on a daily basis. I did not expect that she would ever be off
medication.
She is medication free for 4 years. Still has the occasional problem but we
are able to cope.
Good luck
Laura

Remicade - treatment for psoriatic arthritis

2007-01-23 07:57:12

I just read at www.arthritisdaily.com that Remicade is being tested
for psoriatic arthritis. Has anyone heard about this or know
anything about Remicade?
Thanks
[Editor's Note: Hi Lynn. A number of our members are or have been on Remicade
and I'm sure some of them will share their experiences. Are you in the US or
another country? I ask because Remicade is not new in the States. Welcome
aboard. Wishing you wellness, Kathy F.]

Re: vioxx vs celebrex vs other treatments

2007-01-22 23:19:19

---
Hi Shana,
I use Celebrex and works pretty good. I went a couple of days
without taking it when I didn't have my "scrip" filled and boy did I
notice the difference without it!
God Bless, Sue.

Re: For Sue from Michigan

2007-01-22 20:59:28

---
Hi Kathy,
I did call an Eye Dr. this afternoon and they were worried. The lady
that answered the phone put me on hold and went and talked to the Dr.
she came back and asked me if I was having any pain-I told her I have
stinging-but that might be from the ointment that the Dermy gave me.
She gave me an appt. for the 29th, but she said if she had any
cancellations she would call me. Thanks for being so caring for me.
I am scared because of the spine also hurting-I got x-rays the last
time I was at my Rheumy (Oct.), but haven't heard anything about them-
I'm not sure if anything will show up on regular x-rays or not. I
have a appt. for my Rheumy this coming week.
Thanks again for caring and giving me that "push" I needed to call
the eye Dr. God Bless, Sue in Michigan.

Meloxicam?

2007-01-22 12:11:28

Hi all!
Just a quick question: What good/bad/indifferent opinions can you give about
the NSAID Meloxicam? It goes under the brand name of Mobic in the USA, and
many others in different places of the world (Zix, etc), and for what I
understand, it's kind of a semi Cox-2 drug.
Good? Bad? How about side effects? Incompatibilities? I have read the basic
facts about it, but would like to compound them with real-life experience from
those who have used it!
Manfred.

Question about the pain

2007-01-22 10:32:57

Since I'm new to this whole PA thing, I have a question. I notice that for
me, I dont have alot of consistant and constant pain, but I find that
sometimes the affected joints will almost throb, LIke my toe for
instance..PAIN NOPAIN PAIN NOPAIN PAIN NOPAIN, almost as regular as my
heartbeat. Sometimes it feels like fire in the joint, I'm suspecting that's
where you get the term "flare" ? My thumb especially suffers from the fire
joint syndrome. My pinky only seems to hurt when I extend it past it's
ability to flex, when I forget that it's affected and try to use it as
normal. The middle of my back and my neck seems to hurt only when I move.
The collarbone hurts when I lift something, or turn it wrong.
Is it normal to have different kinds of pain in different affected joints?
Is there a 'normal' anymore?
Comments?
Crystal
[Editor's Note: Crystal, many of us refer to life with PA as our "new normal"
because nothing is like it used to be. I certainly experience different types
of pain in different places. Some pain is permanent while some of it does the
"pain nopain" reggae. Great to have you here. Kathy F.]

I'm new to this group

2007-01-22 02:34:29

Hi Christsan
I have heard of studies being done on the so called Mediterranean diet and
its effects on arthritis, there have been some good results. I posted a link
on here about a year ago that
Showed some positive results from a study in Scandinavia, maybe if you
search for it in the archives it might still be on here somewhere.
If not try doing a Google on arthritis and Mediterranean diet you might come
up with something there.
Micky
London

christsan

2007-01-21 23:07:52

Hello, I'm Leanne. My son has PA.
Until the PA is under some form of control, I don't think
altering from a normal diet has much effect (in aggressive cases).
What a bugger that your condition is still unremitting. I'm still
learning so much about this disease, some seem to get it mild, while
others have such a destructive, aggressive form.
I changed my son's diet around (ie. acid/ alkaline) and it didn't
help in the slightest. When we saw Owen's Rheumy and told him, he
said that it was a waste of time until there was some form of
control, but it won't do any harm.
I'm sorry I don't have anything positive to say in relation to
dietary changes. Other people probably have great stories of
miraculous changes to the way they feel, we're yet to discover much.
Try to have a good day
Leanne

Re: For Sue

2007-01-21 18:32:02

---
Hi Karen,
You are so right about the eye appt. not being on a hard exam
table!! I just dread the next thing wrong with me-add eye problems
to my long list. I know I'm not any different than others on our
support list with alot of different health problems. I do hate when
the eye Dr. comes in close looking at your eye!! LOL!! My daughter
and I was laughing about that the other day. Or when they say not to
blink and all of the sudden you think you have to blink and can't
stop. LOL!! Thanks again for caring.
God Bless, Sue in Michigan.

Re: [rheumatic] Novel Method to fight Inflammation

2007-01-21 07:53:19

Robert,
Thank you for your most helpful post, which
recommends eliminating foods containing arachidonic acid.
Arthritis sufferers should also avoid vegetables
from the nightshade family of plants, which
contain a chemical alkaloid called solanine.
These plants include tomatoes, eggplants and potatoes.
The following are some of the thousands of web
pages brought up by doing a www.google.com search
on +"arachidonic acid" +arthritis
http://www.healthandage.com/Home/gm=0!gc=8!l=2!gid2=2378
"Certain ingredients in our food promote the
inflammatory process. One, for example, is
arachidonic acid, a polyunsaturated fatty acid.
Although the human organism normally produces
arachidonic acid itself, most (up to 90%) is
supplied from food. It is contained in foods of
animal origin only. Arachidonic acid fulfills an
important function in our body, but in excess it
promotes the formation of mediators and
precipitators of the inflammatory process,
especially the "free radicals." ... Among
substances that reduce the inflammatory process
are the antioxidants: vitamins C and E, and
beta-carotene; the minerals zinc and selenium;
and the polyunsaturated omega-3 fatty acids.
Whereas vitamins bind and neutralize free
radicals, omega-3 fatty acids prevent the formation of inflammation mediators."
http://www.oilofpisces.com/rheumatoidarthritis.html
"Rheumatoid arthritis is believed to involve an
overactivity of certain inflammatory agents
derived from arachidonic acid. Eicosapentaenoic
acid (EPA) and docosahexaenoic acid (DHA), the
main components of fish oils, are known to
inhibit the formation of these inflammatory
agents. Research has shown that fish oil
supplementation is beneficial in alleviating the
symptoms of several inflammatory diseases... "
http://www.arthritis.org/resources/arthritistoday/1999_archives/1999_07_08explor\
ations.asp
"Its known that saturated fats from animal
products contribute to many diseases. Now
researchers believe the balance of
polyunsaturated fats in Western diets is out of
whack and may be contributing to an increase in
inflammatory and autoimmune diseases. They say we
consume too many of the fats that promote
inflammation and not enough of the fats that
produce the chemicals to counter it... Our diets
are overwhelmed by the omega-6 fatty acids called
linoleic acid, the type thats in most vegetable
and cooking oils and is the primary oil used in
processed and fast foods. In our bodies, some of
this fat breaks down into arachidonic acid that
fuels the agents that contribute to
inflammation... Meanwhile, we are probably
getting too little of the fatty acids omega 3s
and others that help reduce inflammation and improve circulation."
http://findarticles.com/p/articles/mi_m0ISW/is_265-266/ai_n15341119
"Inflammatory diseases are caused mainly, perhaps
entirely, by products formed from arachidonic
acid... We get arachidonic acid in red meat.
Adult humans can make only a very little of
arachidonic acid, and there is no arachidonic
acid in vegetarian food. It would follow that
vegetarian populations have a low content of
arachidonic acid in blood and tissue."
http://www.uwhealth.org/servlet/Satellite?cid=1116338369627&pagename=A_UWH_HOME%\
2FAArticles%2FAArticleLink&c=AArticles
"Dr. Rakel recommends several strategies to begin
shifting to a diet targeted to reduce inflammation, including:
Reduce saturated fats
Major building blocks of inflammatory agents in
the body come from arachidonic acid, which we
consume in the form of animal foods. Studies of
inflammatory conditions such as rheumatoid
arthritis have shown that symptoms improve in
people who eat small amounts of meat and dairy
products, Dr. Rakel says. "Arachidonic acid is
the fuel to the fire of inflammation," he said.
"We don't want a lot of it in our bodies because
it actually fuels inflammation." However, not all
animal products are culprits. Several types of
cold-water fish have shown anti-inflammatory
benefits, including salmon, mackerel, sardines
and herring - due to their high content of the
more beneficial omega-3 fatty acids.
Reduce omega-6 fatty acids
This includes reducing consumption of margarine
and several types of oils, including partially
hydrogenated corn, cottonseed, grapeseed, peanut,
safflower, sesame, soybean and sunflower oils. To
reduce omega-6 fatty acids in your cooking, use
monounsaturated oils, such as olive or canola
oil. When shopping, keep in mind that omega-6
fatty acids are often used in any products that
have a long shelf life, such as crackers,
pastries and potato chips. Do most of your
shopping around the periphery of the supermarket
and don't spend too much time at the red meat and
dairy counters, Dr. Rakel advises.
Increase omega-3 fatty acids
Eating more cold-water fish is one way to boost
omega-3s in your diet. But there are also several
non-meat sources, including flax seeds or oil,
walnuts and green, leafy vegetables."
Sincerely, Harald

Bextra dose

2007-01-20 23:26:10

I was told by my GP that I could take two 20mg per day for my PsA. On
the website for Bextra it says 1-10mg per day for RA. ??? What dosage
is everybody else taking?
Dave

Re: [PsoriaticArthritis] Tart Cherry Juice

2007-01-20 22:52:47

Rae, I like the cherry juice concentrate but I do find that anything high in
acid is not good for my pain levels. I have no authority for my theory, just
anecdotal assumptions. If it works for you we'd all like to hear about it
though. Cheri
farrell <farrell@...
Has anyone out there tried the tart cherry juice concentrate or montmorency
cherry juice? It is supposed to work wonders for pain. I may pick some up this
week and would like any feedback.
Rae
[

Question for Methotrexate Users...Question for Tom in Anchorage

2007-01-20 12:06:26

Hi Tom,
I also consider Enbrel to be my miracle! I've been on it for 3
months and, other than one early flare of the psoriasis...I'm often
tempted to say I'm cured....skin and joints. Even my nails look
like they are healing.
I'm curious......how long have you been on the Enbrel and are you
completely off the MTX? I go to the doctor next week and am hoping
she'll reduce the MTX again...I've gone from 20mg to 15mg. I'm
hoping she'll bring it down to 7.5 next week. I dream about the day
when I can stop it completely. I'm not sure if it's realistic but I
am hopeful.
Thanks.....
: )
Mary
***my sister honeymooned in Alaska last year. She camped on a boat
for several days....not your typical honeymoon but they LOVED it !

Re: [rheumatic] low dose quick taper steroids

2007-01-20 06:18:10

Emma,
I have been on prednisone for 12 yrs straight, never coming off of them. I
wish I had never started them, but they were the only thing that seemed to work
for me. I am 33 and have dermatomyositis/scleroderma. Anyway the main side
effects that you might experience when only on them for a short time would be:
hunger, hard to sleep, mood swings, diarrea, and you might get a little puffy in
the face, but that goes away as you taper off of them, and depending on how
short a time your on them you might not have this problem at all. Be careful of
your salt and sugar intake, prednisone not only makes you feel hungry all the
time, but you also tend to retain water. Prednisone is great for inflammation
and skin problems. I hope this helps, GOOD LUCK!!
Jenny
emluv23@... wrote:
I have never tried prednisone so far. Soon will be starting 20mg that
will be
tapered down to 0 within two weeks. Do these short courses still involve side
effects? I've read the list of side effects and there are so many possible
ones that I don't know what to expect realistically. I just want to be prepared.
This is a big step for me as I have avoided all drugs besides antibiotics
until now.
Also, just had a major breakout of vasculitis all over my legs...very dark
purple spots. Has anyone had this that can tell me how long it takes for them to
fade completely? I haven't found mention of fading in any of the literature.
Thanks!
Emma

Re: [rheumatic] PAIN IS A PAIN

2007-01-20 03:36:11

Hi
Thanks for responding to my question about the RA.
I am so sorry about all your pain you are going through. I fully understand
those days where it seems no one understands how you are feeling it is so
hard. You sound like a very strong person and that you have went through so
much.
I hope that they find a solution for you. I have went through many melds
myself
and have finally found one that really is working (I am just hoping it stays
working)
it is Arava, it is the best so far, I take it along with 5mg. of predinsone a
day and of course the pain pills if needed. But since I have started the Arava
I have decreased my need for as many pain pills tremendously. I have also
started Aqua Therapy which has been really really helpful in keeping some of the
pain away because you become more mobil when you can start using some of your
muscles again. I have sit so long with out much exercise that it was really
getting bad for me to get around much until I started the aqua therapy. I
really wish the best for you, just remember God is on your side no matter how
you feel sometimes.
Take Care of Yourself
JoJo
ladyfrogofwyo <ladyfrogofwyo@...
i'M 38 YEARS OLD AND HAVE HAD JRA SENCE I WAS 2AND HAVE HAD MORE PAIN
IN MY LIFE FOR SOME ONE THAT IS 3 TIMES MY AGE.I WAS TOLD I COULD NEVER
HAVE KIDS BUT I HAVE TWO AND THEY DON'T HAVE THIS.ITHANK GOD EVERYDAY
CUZ I SURE DON'T WANT THEM TO GO THREW ALL THE PAIN AND SURGARYS I HAD
TO GO THREW.BEFORE I WAS 17 I HAD FOUR AND NOW I NEED MY LEFT KNEE
REPLACED AND MY RIGHT ELBOW DONE.I'M LUCKY TO BE WALKING,WHEN I WAS 17
IWAS TOLD I WOULD NEVER WALK PAST THE AGE OF 22,I'M 38 NOW.I PRAY TO
GOD EVERYDAY THAT I CAN WALK.I HAVE BEEN ON EVERY MED. OUT THERE FOR
THIS AND NOW I'M ON THE LAST RESORT IF IT STOPS WORKING I'M IN A WHEEL
CHAIR.I PRAY EVERYDAY THAT DON[T HAPPEN BUT ONLY GOD KNOWS FOR SURE
WHAT WILL HAPPEN TO ME .I WANT OFF ALL THE PILLS I'M ON CAN ANY ONE
HELP ME FIND SOME THING DIFFRENT TO HELP WITH THE PAIN PLEASE LET ME
KNOW A.S.A.P THANK YOU.
dENICE A.K.A
To unsubscribe, email: rheumatic-unsubscribe@egroups.com

Spice May help Arthritis Inflamation - News

2007-01-19 19:14:27

BlankSpicy Spin on Easing Arthritis
Tests on Rats Show the Curry Spice Turmeric Deserves Further Study, Researchers
Say By Miranda Hitti
WebMD Medical News Reviewed By Louise Chang, MD
on Monday, October 30, 2006
Oct. 30, 2006 -- Turmeric, a curry spice, may curb arthritis joint inflammation,
new research shows.
So say scientists including Janet Funk, MD, of the Arizona Health Sciences
Center at the University of Arizona.
Turmeric been used for centuries in traditional Indian Ayurvedic medicine to
counter inflammation, Funk's team notes.
"Clearly, however, additional preclinical and clinical trials must be conducted
before the use of turmeric for arthritis can be recommended," the researchers
write.
Their bottom line: Turmeric shows promise and deserves further study, but it's
too soon to count on moving it from the spice rack to the medicine cabinet.
The study appears in Arthritis & Rheumatism's November edition.
Turmeric Trial
First, the researchers brewed their own turmeric extract to mimic the chemistry
of commercial turmeric supplements.
Next, they injected the turmeric extract into the bellies of about 90 female
rats. For comparison, they gave other rats shots lacking turmeric.
The rats got those shots every day for two weeks.
Four days after starting those shots, the mice also got shots of an arthritic
compound.
Over the next 28 days, the mice in the turmeric group showed less joint
inflammation and less joint damage than those in the comparison group.
The study ended after that, so longer-term results aren't available.
More Findings
The turmeric extract apparently curbed certain genes involved in joint
inflammation, Funk's team found.
The mice in the turmeric group also showed better bone mineral density than
those in the comparison group.
Turmeric may help prevent bone loss, but that's not certain yet, the scientists
note.
Five of the 87 mice in the turmeric group died during the study. The reasons for
those deaths aren't clear.
The researchers call for more studies to see if turmeric will help ease
arthritis in people.

FEELING MAD!

2007-01-19 19:11:15

Dear Jane, thanks for letting me know. You know that's not a typical email
from me, but I suspected this out about after the 3rd email from who ever is
writing. I don't want to ever isolate someone, but we aren't helping
her/him with constant emails of sympathy. I think what bothers me the most
is all of us are in pain and yet none of us ever write letters like that
demanding more attention. Plus I can't remember one letter from this person
that wasn't all about themselves and never asking or caring about anyone
else in the group. Thanks for backing me up. I sort of went out on a limb
here and knew there might be consequences. Take care, Fran

FEELING MAD!

2007-01-19 08:32:57

Dear Mo, thanks for supporting me. I'm glad to know I wasn't alone on this
one. Take care, Fran

Re: [PsoriaticArthritis] Thanks! &amp; PA questions

2007-01-19 01:50:44

Hi again d,
I have problems with my feet too although currently they are not as bad as
they can be. Most of the problem centered around the heels but all of my toes
are now deformed in one way or another. Recently I have been more comfortable
when my shoes are off though. I must admit, I would probably find it more of
a problem getting up and down from the dinner table in Japan! Lol
I have got to agree though d. I look stupid in sneakers and a dress too! Lol
I get those comments too about looking ok. I think some people think we
should all be walking around looking like The Hunchback of Notre Dam because we
have PA............Don't get me wrong, I do sometimes. Lol.
Take care,
Martin

more about me...

2007-01-18 21:24:17

Thanks for the warm welcome. I am glad to know there is somewhere to
vent/share with others with the same problems. Here is a little about
me. I am a 33 year old married (16 yrs) mother of two children, ages
12 and 15. I live in a rural community in Kentucky. I know of NOONE
else around with psoriasis or pa anywhere close to the extent of
mine. Psoriasis covers over 60% of body. It stays flared up most of
the time, I am sure due to stress. PA involvement on Sacr. region of
spine, tendonitis in both achilles (sp) tendons, nails of feet and
hands, both ankles and my right hand is mildly involved right now. I
have been on Methotrexate more than once...oral and injections,
Soriatane, Cyclosporin, PUVA therapy, Tar baths, Tazarotene (it is a
clinical trial oral med from the Allergan Co.), all types of topical
treatments, and I take Adorax for itching. I have tried to get on
Enbrel, but my insurance refuses to pay but a third of the cost and I
don't qualify for disablilty or medicaid at this time. I am on my
third doc in 8 years, and am going to a Research Institute 2 hours
away from home(thus the clinical trial drug...they pay for everything
involved in my care right now)once a month for pictures, labs, exams,
etc... I am hoping to get in an Enbrel or Remicade study in the
spring. Any corespondence is appreciated. Cheers to the founder of
this site!!!

My meds, past and present....

2007-01-18 15:26:58

Hoping this helps someone. I know it already helped me to see that so
many of you are on so many meds and have tried so many meds!
Present meds:
Kineret: doesn't seem to give me much relief BUT it does seem to keep
my ESR/CRP counts lower.
Cellcept: seems to help a little bit, can't take more than 4 (500mg)
a day or get mouth sores. Also nausea.
Alzulfidine: seems to help a little bit.
Predisone: 5mg, wish I could take more but know it is bad in higher
dosages
Cortisone injections into joints as needed: used to get 'systemic'
injections of it but ALWAYS, ALWAYS got HUGE P flare a few weeks
later, refuse them now no matter how bad my PA is. The ones into
joints don't seem to bother the P.
Folic acid: seems to help keep mouthsores from cellcept at bay.
Celebrex: only on really bad days since I only have 1 functioning
kidney and taking it regularly makes my creatinine climb dangerously.
But it REALLY helps my pain.
Phrenlin Forte: a weird old pain reliever, often used for headaches,
has tylenol and some kind of barbituate. Since I get nauseated with
any of the opiod related pain meds. Usually use it if needed at
bedtime since it makes me sleepy.
Neurontin: to calm the neuropathy the docs said came from the
remicade.
Effexor: to fight depression from dealing with all the rest of these
meds!!! LOL
B vitamins to help combat side effects from the other meds.
Like a lot of you I also have hypo thryoid and take synthroid, slight
High BP and I take lotensin. Various meds as needed for allergies and
asthma. Refresh eyedrops all the time for dry eyes.
Meds in the Past:
MTX and Arava--didn't help that much but probably kept me from
getting worse faster. After a year my liver enzymes hit the roof and
I had to get off them both.
Remicade--Worked great for a few months, even cleared my P
completely, first time in over 2 decades!!! Then stopped working as
well, Salesrep told my Rheumie to increase my dosage, w/in a month I
developed severe neuropathy issues, was referred to Neurologist who
referred me to one at Stanford, they decided it might be a mylenation
problem and told my Rheumie no more anti-TNF drugs for me. :(
Colchicine: My doc found evidence of CPPD crystals in fluid from my
knee. The Colchicine didn't do anything but make me nauseous.
Ultracet/ several other pain relievers: Unfortunately all of them
made me nauseous, to the point of actually vomitting.

Re: New to this list...Hi

2007-01-18 10:28:28

Hi Fran, sounds like you have had quite a time! Actually, as far as
my doctor and I can tell, I don't have psoriasis except from time to
time of the fingernails which clear up with cortisone ointment. I
do have dry flakey skin like most people have in the winter, but
mine lasts year round. I am very fair complexioned and my skin is
really thin. But I don't have any typical looking psoriasis spots.
My main problem is the pain and stiffness and not being able to do
anything I want to do! I am exhausted all the time. I sleep great
though. Just no energy, no stamina, no strenth. I had all the
preliminary blood work and chest x-ray etc. and am waiting to hear
from my rheumatologist as to what dose of methrotrexate and when to
start it. I am nervous about it...more than anything because of the
immonosuppression part of it. Last fall I caught an upper
respiratory virus from my grandsons and was so sick I thought I
would die. Had to take breathing treatments, prednisone and
antibiotics. Took me a month to recover and was told I have
reactive?? (I think that was what they said) asthma that will flare
up when I get a cold or respiratory infection. That was a year ago
next week that I got sick and haven't had any problems with asthma
since then. Have not had to use my puffer at all. I am wondering
if there are things (besides folic acid) that they put you on to
minimize the side effects and also to protect the immune system?
Any body taking Neulasta? Are there other drugs for the white cells?
Hanna

Re: [rheumatic] Detox food pads, anyone else try them?

2007-01-18 05:49:12

The idea sounds wonderful, but this website isn't a place to order them,
it's a place to join their sales team. So what's the deal? Where do you
actually buy them?
Jill

Re: [rheumatic] Spice May help Arthritis Inflamation - News

2007-01-17 21:31:06

Hi Julie, here is more info. I have been using 2 teaspoons of turmeric
a day.Seems to help.Lynne G. /SD
http://www.whfoods.com/genpage.php?tname=foodspice&dbid=78
<http://www.whfoods.com/genpage.php?tname=foodspice&dbid=78

Re: PA and Acupuncture

2007-01-17 20:54:14

yes! i attend accupuncture at least weekly, sometimes more often.
i have found it to be a good support for my body. particularly for
pain relief and treatment for post MTX sickness. in some countries,
accupuncture is used instead of anaesthetic during some surgerys. it
allows the body more of a chance to heal.
also, animals love accupuncture. i think it's a really good sign when
your dog or cat companion lays completely still in ecstasy whenever
they are needled.
the great thing about accupuncture is that it doesn't interfere with
your current treatments, and there's barely any side effects. the
needling and bloodletting that i've had don't hurt as much as the
western medicine does. the way traditional chinese medicine considers
your experience of your body is radically different to western
medicine. which is really quite good for your head! ideally, the two
work together: you take your western medicine AND you take your
traditional chinese medicine.
i had JA from age 4, and i would have LOVED accupuncture.
it is wonderful and inspiring to hear that he's found a treatment so
successful at such a time in his life.
ALSO A HINT: get your accupuncture/chinese herb needs from a student
clinic! it's SO much cheaper. in melbourne i can get it for $15 for a
90 minute consultation.
compassion,
alana x

To Everybody, The Cleveland Clinic..a Nightmare!

2007-01-17 10:10:51

Dear Janet and every one else in the group,
Well I'm back from Naples and the Cleveland Clinic. The easiest way to say
it is it was a total waste of time. I had several of my doctors here tell
me that they thought the Cleveland Clinic in Naples was full of the "playboy
doctors" who enjoyed their weekends and half work weeks more than dealing
with patients. I have to say that I totally agree with that summary. I saw
three doctors the whole time I was there and they got worse with each visit.
The first one was the dermatologist who told me again that he didn't think I
had psoriasis on my arms and legs. I told him that my rheumatologist had
said that since I've been on prednisone the results could have been wrong
from the biopsies, but he didn't think so. He thinks all I have is a type
of genetic sun damage that can be precancerous, but isn't really that
serious. I asked him about my erythromelalgia, which is what turns my skin
bright red and burns all the time, and he didn't know anything about it. I
had to tell him that is was listed in NORD, the national organization for
rare disease, so he knew how to look it up. He came back and said that
aspirin has been a treatment choice that works best, and I know for a fact
that they don't use aspirin anymore and that hasn't been the treatment of
choice for over 5 years. I didn't point that out to him, but he told me to
see the rheumatologist next and then we would talk again right after.
Well we all have rheumatologist stories about how rotten they can be or what
jerks they can act like, just imagine all those stories rolled up into one
and you've met my doctor. First of all, he was the one that made me
reschedule all my appointments because he had "plans'' out of town, which of
course he didn't apologize for or even mention, not that I expected him too.
The first thing he did was complain about my medication. I tried to tell
him all the drugs I've been on, but he had to ask the questions and only
wanted yes and no answers. If I tried to explain something, he would cut me
off and say, "I don't need to hear this". Finally, I said well then what do
you need to hear? and he just said Yes or NO. So I was frustrated but I
tried to do that too. Then he decided to examine me while I was saying yes
or no and I've never had someone hurt me so much in an exam. Where most
doctors know they are dealing with a chronic pain patient, they go out of
their way to be careful, he was just the opposite. I almost felt like the
thought I was faking the pain. My daughter was in the room with me and said
I was literally jumping off the table and he would said does that hurt? All
I could get out was Yes and stop it, and he was on to another place. I was
black and blue the next day all over my sides, arms and along my spinal
area. My hip hurt so bad the next day I could barely walk. When it was all
over he said I had arthritis from an undetermined source, maybe rheumatoid
and maybe PA, and probably osteo as well. (I said I knew all that before I
came here. I was so upset by this point I was almost in tears and almost
felt like a rape victim I was in so much pain. I really do plan to write a
letter to the main office in Cleveland and complain about him. I've never
had such a rude, and basically mean doctor in all my life. That was all he
did and he walked out. He didn't offer me any advice, any new medications,
want to run any more tests, or make any suggestions. He made me feel like I
had too many problems, should never had been on prednisone and he definitely
didn't want to treat me. The idea of working with me to help me feel
better, never entered his mind. He did tell me me I had inflammation along
my chest wall, I guess that was from all the cries I gave out when he was
stabbing me, but when I asked him what he recommended for that, he told me
to meditate. I've got nothing against meditation and have done it all my
life, but I wasn't prepared to hear that from him. He said he was stress
related, but I think my rheumatologist here at home told me it was PA
related. So needless to say, I'm staying with my current doctors. One
thing the whole visit did do was make me realize just what great doctors I
really do have.
My next appointment was with the internist. I was at the end of my rope by
this time and ready to just leave, but my daughter convinced me to give him
a try. So he walks in and says, he can't believe I'm on heavy narcotics for
my pain. I told him, or tried too about my jaw and how bad the bones are
and the fact the nerves are exposed and inflamed from all the joint damage,
but he didn't care. He looked at me and said, "I'm not giving you
morphine." I just said," I didn't ask you for any and not what I am here
for, that's why I went into pain management so I could always be regulated
and make sure I was safe with what I took." He told me I would get the same
benefits from going to watch a sunset! My daughter and I was were just
shocked. I said, that's your advice, with all that's wrong with me? He
said, well you are too complicated of a case for me and have too many
problems. He said that he wouldn't want to treat me and that fact that I"ve
been on prednisone for 3 years was just asking for all sorts of problems. I
told him I'm down to 15mg from 60mg, but nothing I said again mattered. He
couldn't get past the pain medication. Then at the end he said, "Oh, well I
don't know anything about pain management anyway." So he said, What do you
want from me? At the point, I just said nothing, I"m ready to get out of
here and we left.
So that was the whole great experience. I didn't learn a thing. OH and the
rheumatologist told me that Vioxx was very dangerous for heart problems,
even at 25mg, and then 5 minutes later the Internist told me that Vioxx was
perfectly safe and the last study was flawed. I never even told him what
his "great colleague" had said...It was a real night mare. When I got out
all I wanted to do was cry. It was a complete waste of my time and I am
still sore from all the poking. All I can say, is I hope that anyone who
goes to Cleveland Clinic goes to the one in Cleveland and hopefully they
aren't the same type of doctors there. I guess my experience could have
been a fluke and maybe someone else would have had a great experience, but
my daughter felt like she needed a drink when it was over with and all she
did was watch!.
The good news is I stayed an extra day with my daughter and we had fun going
out and shopping. I couldn't do as much as normal because of the exam, but
I still saw my sister and my niece for lunch. So it wasn't all bad. I'm
sorry I don't have any great news. I did manage to ask the Internist about
the leg vein problem and he blamed it all on the prednisone. I know some
people in the group were wondering about that question and how it can cause
edema. I also know that not everyone is on prednisone, so he didn't really
give me a good answer, but that was normal for the whole visit. That was at
the end and by then I had taken all I could of those doctors. I never did
see the dermatologist again. He got tired of waiting on me and just left.
So he didn't really care about the situation either. I don't know if it
would have been better if my husband would have gone with me or not. He
would have probably hit the rheumatologist, so I doubt it would have made
the situation any better...lol.
Talk about depressing. I wish I had better news to report, but for me it
was a waste of time and painful in the process. Take care and I'll write
more later. I'm still pretty overwhelmed by the whole experience. Take
care and I hope everyone has been feeling ok and doing well the past few
days. Love, Fran
Fran,
by the time you read this you will probably be back from the clinic
already.
You are in my thoughts and prayers and I hope they can help you there in
the way you want them to. I'm sure everyone here feels the same way. We
will be anxious to hear the news when you return.
Janet

Rx cap of $1,500 per YEAR

2007-01-17 01:54:02

Hi all,
Karen, Thanks for telling me about your dad. I had injections in my neck many
years ago so we will see. Currently I'm still on PT, my walking has gotten a
little better but other functions ar still quite painful.
I work for Home Health Care Mgt which is an umbrella for 4 other companies
offering home health care for RN, PT, OT, PSY, Aides etc. I work in the IT
department. We just got notification that there is going to be a CAP on Rx for
$1,500 per person per year. They have GOT to be KIDDING. NOPE.
Another woman in my department and I met with head of HR and said, what is
happening here, why are we not at least OFFERED a plan with better Rx. We gave
our plea and now we wait. I had to give a list of my meds so she could go back
to the broker and see what they could / can offer. Anyone with PA knows that
won't go far. I've been on embrel since last spring but oh my goodness - if
this goes through I'll be back on Reemicade fast as that doesn't go through my
Rx plan. The insurance will pay for the drug and process and my only out of
pocket is $20.
I've called the SS office and they gave me such a hard time as I make over $880
a month. Geez.........I don't make great money by any means but I'm really
concerned about what is in store for us in 2005.
USA needs better health care regulations..............someone is getting RICH
off the rest of us and it is scary.
Nancy in Penna

RE: [rheumatic] Nasal wash

2007-01-16 21:57:52

Thanks Ute,
I have used all of this!!

Hi--I'm new to the group

2007-01-16 18:22:23

Hello,
I'm just joining the group. I've been reading many of your posts
and appreciate the information sharing, so I thought I should say
hello and not just lurk!
I was diagnosed with PA last week after 5 yrs of being told it was
OA. I don't have P. Should I add "yet?" Still in the "I'm pretty
overwhelmed by this" stage and trying to learn as much as I can. My
father's family is full of RA so for the past year I've been
thinking I had more than OA and fearing RA... now I am learning
about PA! yikes
Gwen
"You must do the thing you think you cannot do." ... Eleanor
Roosevelt
[Editor's Note: Hi, Gwen. Welcome to the list. It can be overwhelming, but as
with anything, the key is to educate yourself as much as possible and not settle
for mediocre medical care. I am a bit concerned by the change in diagnosis
because OA usually shows up in bone density tests. It presents itself very
differently from PA or RA. Who changed the diagnosis? Are you under the care
of a rheumatologist? Did the physician who diagnosed you say why he/she
believes it is PA given you don't have P? It is very possible to have PA
without P, but usually there are signs present such as nail involvement, P on
elbows, etc. OA on the other hand, is almost always visible in bone density
tests. The same is not true for PA. Did your physician recommend a drug
regimen and if so, do you have any questions about the medication? We look
forward to hearing from you frequently. Again, welcome, Kathy F.]

FEELING MAD!

2007-01-16 11:54:01

Dear Fran, I think that when something looks like a fish, swims like a fish and
acts like a fish, it's OK to say that something seems fishy. I hope and pray
that Brenda/Bjorn gets the help she so desperately - and clearly - needs.
Everyone here knows what a kind, supportive and loving heart you have, Fran so
please don't worry about that.
Kathy F.
Dear Mo, thanks for supporting me. I'm glad to know I wasn't alone on this
one. Take care, Fran

Re: [rheumatic] Diagnosis - sort of

2007-01-16 05:19:50

Hello,
It is always good for any doctor to know everything you are on whether it be
over the counter or even just drugs for another condition. A stronger immune
system does play a role in it. That is part of the reason we are in the shape
we are in. Me included:)) I tried different supplements and had to find out
the hard way that not all brands are the same. Cheapest isn't always the best.
It depends on how much you value your health. Something isn't working if your
immune system isn't able to do its job. Any kind of arthritis I have found from
speaking with specialists is a degenerative disease. The NSAIDs only cover up
the symptoms making the pain bearable - they do not cure nor get to the root of
the problem. This couold be why you felt like you did when you missed a dose.
Yes I ache all the time, but that is a lot better than pain and the ache I can
handle. Pain forget it.
I hope you have good results from your tests and you aren't alone out there.
Any time you want a friend to speak with or hear you out feel free....my email
addy is below. Smile the rest of the day will be good.
Hugs.....Julie
Julie Hope
Degenerative Disease Information
juliehope@...
Saskatchewan, Canada
Tel: 1 306 648-2642 (CST)
http://www.4betrhealth.com

[PsoriaticArthritis] for Annie...

2007-01-15 23:05:10

thanks Karen! I have been so amazed at the progress in such a short period of
time. I am trying so hard! A friend asked me what has kept me faithful to my
program and I told her....I want to live. Period end of story!! I said everytime
I see something I want that is not healthy for me, I say to myself 474 474 474
and that keeps me on track!!!
thanks for the support!
annie and the pugherd!

Re: [rheumatic] How the Stock Market Works - easy 4 step guide

2007-01-15 15:54:15

This person sent the message and unsubscribed. I've banned the email
address.
Chris.

50mg Enbrel

2007-01-15 11:21:51

I just got a letter from Immunex telling me that a new preloaded 50mg
syringe of Enbrel will be available in a few months. That should be good
news for those of you who are taking two 25mg injections at one time.

Re: [rheumatic] AP for eight years

2007-01-15 03:41:13

Dear Joi
I too have started AP within a year of the onset of RA and in my 9th month. 8
of these 9 months saw a great improvement but now more swelling and pain has
returned which may be due to the fact iI changed from Minocin to a generic
minocycline. What do you think?
Wonderful to see how well you have done on Minocin and I hope someone with
more than 10 years of Minocin responds to your request.
Ken
Joi <joifaithhope@...
Hi,
I have been on AP for almost eight years now. For the
most part, I have tolerated minocin (100 mg) well,
except for gum discoloration and yeast issues. I came
off of minocin for 6 months about two years ago
because of the gum discoloration. The disease flared
and so I went back on it.
I started AP within a year of the onset of RA and as a
result I have no deformities.
I worry about the long-term effects of minocin and how
long I can actually stay on it. Has anyone been on AP
for 10+? I would love to hear their experience.
Thanks!

New Packaging for Enbrel

2007-01-15 01:22:54

I heard from Enliven Services this week that starting in December,
Enbrel will be packaged PREmixed and in 50mg. doses so that if
you're currently taking a 25 mg shot 2x a week.....you could start
taking one pre-mixed 50 mg. dose a week. Has anybody spoken to
their doctors about this change? Does anybody know if this will be
the new recommended dosing AND/or if there will be an added cost?
Obviously this would be a huge improvement but I don't want to get
my hopes up. I'll be seeing my Reum. later this month but would
like to have a clue ahead of time.
Thanks,
Mary

Gluten Intolerance)

2007-01-14 21:09:43

In a message dated 11/11/2004 6:49:29 PM Eastern Standard Time,
christsan@... writes:
(I think millet
is gluten free but am not sure).
yes, it is gluten free, and buckwheat too...

Re: [rheumatic] Need a Little Help with Dosage of Minocycline for Scleroderma

2007-01-14 06:26:34

Lucy,
My 17 year old daughter was diagnosed with systemic
scleroderma (SD) in May 2006. We learned about the
Antibiotic Protocol (AP) in June and requested a
listing of doctors in our area from the Road Back
Foundation. We took her to a doctor in Northern
California (3 hours from our home, there were no
doctors closer at the time, but one has been added
now, a very experienced one that was there all along,
but the RBF was not aware of him). Then we also
traveld to Boston to see Dr. T. He prescribed the
same doseage that was used in the "Harvard Study"
which is 100mg/2xday/everyday. He also insists on
Brand Name Minocin, and he is adamant about no food or
drink (other than water) for two hours before and
following the dose (that is the tricky part, most
difficult). We went for a follow up appointment in
November and he kept her on the same doseage. I ahve
also spoken with and emailed others who see Dr. T for
SD and they are also on the same dose.
So I think that you are on the right track. Also,
keep in mind, since you seem to be working with a
cooperative, but not completely experieced GP, Dr. T
in Boston will do consultations with other doctors, so
if your doctor is willing, and the two of you come up
with some questions, call Dr. T.
Good Luck,
Cheryl Ferguson

Re: [rheumatic] minocin vs doxycycline Dr Chiu

2007-01-14 05:57:17

Hi, I can't take Minocin, but have no trouble with Doxy. My doctor orders the
bills instead of the capsules for me. Carol
In a message dated 6/20/06 11:52:16 PM Eastern Daylight Time,
esther_warkov@... writes:
Hi,
I've had great improvement in my knee with minocin (it was diagnosed
through biopsy with inflammatory arthritis). However I'm a person
that doesn't tolerate minocin very well, even 50 mg doses. I still
have some symptoms in my fingers and toes at this time. Dr. Chiu
recommended doxycycline. Does anyone have experience with using that
instead of minocin?

Re: [rheumatic] Minocycline only?

2007-01-13 19:33:36

Hi Maggie
I started AP 100 mg per week in November 2005 and by February 2006, had
stopped taking an Nsaid, Anthrotex, until Sept 2006, (now). The need for an
Nsaid now COULD be due to fact that Minocin is temporarily unavailable in
Britain and I'm taking a generic - minocycline. between February and September,
I did not need to take any anti-inflammatories.
Regards
Ken.
Maggy Alonso <MaggyAlonso@...
Is anyone taking only minocycline for RA? I take it twice a day 100
mg. I am also on Celebrex 1x daily and if I miss a dose of the Celebrex than I
experience lots of inflammation and stiffness. I was hoping to be able to
discontinue the Celebrex eventually but I am not ready yet. I have been on AP
for a little over 3 months now. I'm just wondering at what point others were
able to rely on only the antibiotics and still remain somewhat comfortable.
Maggy

Tetracycline questions

2007-01-13 14:03:09

Hello,
I've been on the name brand Minocin (100mg once on M-W-F) for 2
years & have seen no halt to the RA. It has progressed to other
joints (fingers & toes) while on Minocin. I've had less pain at
times, but am not sure if this is due to dietary changes, the
Minocin, or a combination of both.
I now have a new doctor who has read Dr. Brown's book, believes in
the treatment, and is willing to work with me. Today, he prescribed
250mg Tetracycline - once on M-W-F for 2 weeks, then twice on M-W-F
for 4 weeks, and a return visit to see him, 6 weeks from today. (He
also did blood work today.)
Has anyone here tried Tetracycline for RA? What were your results?
If this drug works, that will be great since 60 capsules of
Tetracycline at Wal-Mart costs me a total of $5.12, as opposed to
over $275 for 30 capsules of Minocin!
Last night, while searching through Dr. Brown's book (have read it
twice, and am now reading it for the 3rd time) I couldn't find a
reference to Minocin, but did find that Dr. Brown talked a lot about
using the tetracycline drugs.
On what page number does he say to use Minocin as the drug o