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Re: RA and Now MS

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Hi ,e

I'm taking Enbrel too and there was concern that I might have MS at one

point too d/t my MRI. I'm curious to know what it was that tipped off your

doctor's to the diagnosis of MS for you- if you wouldn't mind sharing.

Thanks,

Abby

In a message dated 5/1/2008 8:13:30 P.M. Pacific Daylight Time,

kuehnlej@... writes:

I have been diagnosed with RA for about 3 years and was diagnosed with

MS this past week. I am just wondering if there is anyone else on the

list who has both diseases. My rheumy said I had to come off Enbrel

and can't go on any biologicals anymore. I have read as much as I can

find but there just doesn't seem like there is much information.

From what I am reading it seem like Orencia has been used for both

diseases. I don't really know how it is different than the others but

I am just SO against going back to all the pain I was in with my RA.

It isn't gone but it sure is better.

Does anyone have any information?

**************Wondering what's for Dinner Tonight? Get new twists on family

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My goodness. I have RA about 6 years since diagnosis.

I blamed everything on RA. My Doc said RA is not causing many of my symptoms

and tomorrow I am having an MRI for MS.....I have about 80 percent of stmptoms

on their check l;ist.......

kuehnlej <kuehnlej@...> wrote:

Hello,

I have been diagnosed with RA for about 3 years and was diagnosed with

MS this past week. I am just wondering if there is anyone else on the

list who has both diseases. My rheumy said I had to come off Enbrel

and can't go on any biologicals anymore. I have read as much as I can

find but there just doesn't seem like there is much information.

From what I am reading it seem like Orencia has been used for both

diseases. I don't really know how it is different than the others but

I am just SO against going back to all the pain I was in with my RA.

It isn't gone but it sure is better.

Does anyone have any information?

in St. Louis RA, MS taking prednisone 20mg daily,

methotrexate injections once a week, folic acid 3 mg daily, singulair

10 mg, gabepentin 1200 mg daily, wellbutrin 150 mg, prozac 40 mg.

Raniolo

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,

How did your physicians decide that it is MS and not an adverse effect of

Enbrel?

Over the years, we have had reports from a few members who have been told

they have both RA and MS. We have also had some reports of MS-like symptoms

suspected to be associated with the use of anti-TNF biologics.

Not an MD

> [ ] RA and Now MS

>

> Hello,

>

> I have been diagnosed with RA for about 3 years and was diagnosed with

> MS this past week. I am just wondering if there is anyone else on the

> list who has both diseases. My rheumy said I had to come off Enbrel

> and can't go on any biologicals anymore. I have read as much as I can

> find but there just doesn't seem like there is much information.

> From what I am reading it seem like Orencia has been used for both

> diseases. I don't really know how it is different than the others but

> I am just SO against going back to all the pain I was in with my RA.

> It isn't gone but it sure is better.

> Does anyone have any information?

>

> in St. Louis RA, MS taking prednisone 20mg daily,

> methotrexate injections once a week, folic acid 3 mg daily, singulair

> 10 mg, gabepentin 1200 mg daily, wellbutrin 150 mg, prozac 40 mg.

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My symptoms were present prior to the start of Enbrel too. There were

changes on the MRI as well. Enbrel can worsen the effects.

Abby

In a message dated 5/2/2008 9:50:30 A.M. Pacific Daylight Time,

minyslater@... writes:

I have had RA and MS for 4 years. Both diagnosed within a four month

period prior to taking any biologics. I just finished my 1st year on Orencia.

So

far so good. My rhemy chose Orencia because it would only stayed in my

system for 30 days should something go wrong. Orencia has made a dramatic

improvement on my RA. Would recommend without hesitation.

**************Wondering what's for Dinner Tonight? Get new twists on family

favorites at AOL Food.

(http://food.aol.com/dinner-tonight?NCID=aolfod00030000000001)

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I have had RA and MS for 4 years.  Both diagnosed within a four month period

prior to taking any biologics.  I just finished my 1st year on Orencia.  So far

so good.  My rhemy chose Orencia because it would only stayed in my system for

30 days should something go wrong.  Orencia has made a dramatic improvement on

my RA.  Would recommend without hesitation.

[ ] RA and Now MS

Hello,

I have been diagnosed with RA for about 3 years and was diagnosed with

MS this past week. I am just wondering if there is anyone else on the

list who has both diseases. My rheumy said I had to come off Enbrel

and can't go on any biologicals anymore. I have read as much as I can

find but there just doesn't seem like there is much information.

From what I am reading it seem like Orencia has been used for both

diseases. I don't really know how it is different than the others but

I am just SO against going back to all the pain I was in with my RA.

It isn't gone but it sure is better.

Does anyone have any information?

in St. Louis RA, MS taking prednisone 20mg daily,

methotrexate injections once a week, folic acid 3 mg daily, singulair

10 mg, gabepentin 1200 mg daily, wellbutrin 150 mg, prozac 40 mg.

________________________________________________________________________________\

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>

> Hi ,e

> I'm taking Enbrel too and there was concern that I might have MS at

one

> point too d/t my MRI. I'm curious to know what it was that tipped

off your

> doctor's to the diagnosis of MS for you- if you wouldn't mind sharing.

> Thanks,

> Abby

>

>

>

I developed a tremendous weakness in my legs that really didn't hurt,

it was like my legs had a very small amount of energy and at the end

of that (10-12 steps) I would fall. It was horrible. I went to my

rheumy who was the first to suggest MS and she sent me to a

neurologist. He didn't think it was MS but scheduled me for nerve

conduction tests. While I waited for the test day, I began having a

lot of trouble with eye pain and then the next day had about 50% of my

visual field in my left eye just disappear. I went to the

ophthalmologist who said I had optic neuritis and that it was a " Major

player " in MS. He ordered an MRI of my brain and found 9 lesions then

found 3 in my spinal cord. They compared it to an MRI I had about two

years ago where there was 1 lesion in my spinal cord and none in my

brain. The neurologist also ordered a bunch of blood tests. I will

have the nerve conduction tests finally Monday (it took 6 weeks to get

in for them). Since then the weakness has improved.

Are you being tested for MS now?

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--- In , " " <Matsumura_Clan@...>

wrote:

>

> ,

>

> How did your physicians decide that it is MS and not an adverse

effect of

> Enbrel?

>

> Over the years, we have had reports from a few members who have been

told

> they have both RA and MS. We have also had some reports of MS-like

symptoms

> suspected to be associated with the use of anti-TNF biologics.

>

>

>

> Not an MD

>

>

>

Well, I don't know and will definately ask. It may be because I

stopped taking Enbrel about a month before the weakness began. I will

have to ask because it would be great to find out it will go away

since I have stayed off Enbrel.

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It sounds terrible, .

Why did you have an MRI two years ago? How long were you on Enbrel and why

did you stop it?

Not an MD

> I developed a tremendous weakness in my legs that really didn't hurt,

> it was like my legs had a very small amount of energy and at the end

> of that (10-12 steps) I would fall. It was horrible. I went to my

> rheumy who was the first to suggest MS and she sent me to a

> neurologist. He didn't think it was MS but scheduled me for nerve

> conduction tests. While I waited for the test day, I began having a

> lot of trouble with eye pain and then the next day had about 50% of my

> visual field in my left eye just disappear. I went to the

> ophthalmologist who said I had optic neuritis and that it was a " Major

> player " in MS. He ordered an MRI of my brain and found 9 lesions then

> found 3 in my spinal cord. They compared it to an MRI I had about two

> years ago where there was 1 lesion in my spinal cord and none in my

> brain. The neurologist also ordered a bunch of blood tests. I will

> have the nerve conduction tests finally Monday (it took 6 weeks to get

> in for them). Since then the weakness has improved.

>

> Are you being tested for MS now?

>

>

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