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Nov. 2009 I was told I have RA. I was put on Plaquenil but it did nothing for

me. I felt like it made me worse. The doctor said he doubts that. Then he put me

on MTX. Started to feel a little better with 4 pills but then they wore off and

had to up the dose. I got as high as 8 pills but started to get side effects and

I asked to finally get off after we downed it back to 6 pills. He then put me on

Humaria. I have had 3 shots (a shot every 2 weeks) so far. I have not seen a

change. In the past year and 4 month I have gone down hill. I felt better before

starting on meds. I feel more pain since being on meds. In my eyes I feel like

the meds have made my RA worse. When I was younger I had JRA and was never

treated (long story) and never had any damage. Basically I grew out of it if you

want to call it that. Now that I'm older I took the right option to get treated.

I am wondering if anyone knows anything about meds making symptoms worse and

progressing the RA faster being on them. I would like info before going back to

the doctor. My symptoms now are lots of pain and major fatigue. The last time I

was at the doctor I complained about the side effects of the MTX and he said if

getting off if it doesn't help then my RA might be progressing. The only thing

that stayed was the fatigue. My doctor will listen to me but what I need right

now is experience from the people that have it. Any info will be great.

Thanks,

Cheli

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Cheli, I think that what is happening is that your RA is getting

worse. I don't see how the meds could make it worse; they're just not

making it better. Sometimes it takes a while to find the right

cocktail of meds that will work for the individual person. Your doctor

has kept trying different meds, which is the usual procedure. Also, it

does take time for some of the meds to kick in. With mtx, some people

have fewer side effects with the injectable kind. Also, taking folic

acid should help with the side effects.

Some people have a more severe case of RA than others, and you are

apparently one of those. Your doctor seems to be doing the right

thing, trying to treat it aggressively. I do hope that he will soon

find the mix that will relieve your symptoms. Keep hanging in there.

Sue

On Mar 28, 2011, at 7:50 AM, HLHSINFO@... wrote:

> Nov. 2009 I was told I have RA. I was put on Plaquenil but it did

> nothing for me. I felt like it made me worse. The doctor said he

> doubts that. Then he put me on MTX. Started to feel a little better

> with 4 pills but then they wore off and had to up the dose. I got as

> high as 8 pills but started to get side effects and I asked to

> finally get off after we downed it back to 6 pills. He then put me

> on Humaria. I have had 3 shots (a shot every 2 weeks) so far. I have

> not seen a change. In the past year and 4 month I have gone down

> hill. I felt better before starting on meds. I feel more pain since

> being on meds. In my eyes I feel like the meds have made my RA

> worse. When I was younger I had JRA and was never treated (long

> story) and never had any damage. Basically I grew out of it if you

> want to call it that. Now that I'm older I took the right option to

> get treated. I am wondering if anyone knows anything about meds

> making symptoms worse and progressing the RA faster being on them. I

> would like info before going back to the doctor. My symptoms now are

> lots of pain and major fatigue. The last time I was at the doctor I

> complained about the side effects of the MTX and he said if getting

> off if it doesn't help then my RA might be progressing. The only

> thing that stayed was the fatigue. My doctor will listen to me but

> what I need right now is experience from the people that have it.

> Any info will be great.

>

> Thanks,

> Cheli

>

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Hi, Cheli. I am sorry to hear that you are having a hard time.

Maybe it's time for a second opinion. Is your current rheumatologist

the only one you've seen lately?

Not an MD

On Mon, Mar 28, 2011 at 6:50 AM, HLHSINFO@... <hlhsinfo@...> wrote:

> Nov.  2009 I was told I have RA. I was put on Plaquenil but it did nothing for

me. I felt like it made me worse. The doctor said he doubts that. Then he put me

on MTX. Started to feel a little better with 4 pills but then they wore off and

had to up the dose. I got as high as 8 pills but started to get side effects and

I asked to finally get off after we downed it back to 6 pills. He then put me on

Humaria. I have had 3 shots (a shot every 2 weeks) so far. I have not seen a

change. In the past year and 4 month I have gone down hill. I felt better before

starting on meds. I feel more pain since being on meds. In my eyes I feel like

the meds have made my RA worse. When I was younger I had JRA and was never

treated (long story) and never had any damage. Basically I grew out of it if you

want to call it that. Now that I'm older I took the right option to get treated.

I am wondering if anyone knows anything about meds making symptoms worse and

progressing the RA faster being on them. I would like info before going back to

the doctor. My symptoms now are lots of pain and major fatigue. The last time I

was at the doctor I complained about the side effects of the MTX and he said if

getting off if it doesn't help then my RA might be progressing. The only thing

that stayed was the fatigue. My doctor will listen to me but what I need right

now is experience from the people that have it. Any info will be great.

>

> Thanks,

> Cheli

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Yes this has been my one and only. I do believe he has been doing a good job. He

does know his meds, side effects, how they work to don't work. He will talk to

me like I am part of the team. I do feel he has been a good match for me. I just

like to have all the info at hand before I go to any doctor.

Cheli

Sent from my Verizon Wireless Phone

----- Reply message -----

From: " " <Rheumatoid.Arthritis.Support@...>

Date: Mon, Mar 28, 2011 5:58 pm

Subject: [ ] Confused....need advise

< >

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I thought about trying the injected MTX but haven't got myself up to trying it.

I'm still new to giving myself the shot every other week. I was on Folic Acid

but I was having to take 4-5 a day just to help with the side effects. I guess I

have to just wait. It is just so hard when you have a family to take care of.

Cheli

Sent from my Verizon Wireless Phone

----- Reply message -----

From: " marysue " <marysue@...>

Date: Mon, Mar 28, 2011 12:46 pm

Subject: [ ] Confused....need advise

< >

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Cheli,

I'm not saying you should leave your rheumatologist, just see what another

thinks of your situation.

If you aren't doing well, it won't hurt to let someone else think about what

could be going on and offer advice to you.

Not an MD

On Mon, Mar 28, 2011 at 7:43 PM, HLHSINFO@... <HLHSINFO@...>wrote:

> Yes this has been my one and only. I do believe he has been doing a good

> job. He does know his meds, side effects, how they work to don't work. He

> will talk to me like I am part of the team. I do feel he has been a good

> match for me. I just like to have all the info at hand before I go to any

> doctor.

>

> Cheli

>

>

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I wasn't thinking that you were saying to leave him. I knew what you meant but

thank you for the response. :)

Cheli

Sent from my Verizon Wireless Phone

----- Reply message -----

From: " " <Rheumatoid.Arthritis.Support@...>

Date: Tue, Mar 29, 2011 6:34 am

Subject: [ ] Confused....need advise

" HLHSINFO@... " <HLHSINFO@...>

Cc: < >

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