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Re: new to methotrexate -

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Hi :

I also had to start Mtx after Plaquenil became less

effective. It took about 2 months before I started to

get benefit from it. I have been on Mtx now for about

4 years, on the pills at first, then was on Mtx

injections for a while which worked better, but am

finding it difficult to obtain injectable mtx right

now, so am back on the pills. I was up to 20 mg. a

week, but am now down to 10 mg. weekly along with

Enbrel. With the Mtx, I am more tired for the day or

two after I take it. Always take it at night, after

you have eaten, and before bed, and that way you

should be able to sleep through any nausea you might

experience. I have never had that problem. Take

Folic Acid as well, and I also take Milk Thistle to

help protect my liver. I have had some hair thinning,

and my skin is more fragile, and I am more sensitive

to the sun, since beginning the Mtx. I have had less

side effects with that than with other meds.

Otherwise, it is helping me, so I take the good with

the bad. Best of luck - and hope it helps -

Kathe in CA

--- sasupbin <sasupbin@...> wrote:

> Hi, I've been following posts on here for a while

> but this is my

> first post. I'm 39 and was dx with RA 5 yrs ago.

> Initially I took

> only NSAIDS (It took 5 different ones before I found

> Celebrex

> worked. Then fpr the past three years I was on

> PLaquenil and did OK.

> Some flare ups here and there but a week of

> prednisone would calm it

> down. A few months ago I started having pain all

> day every day in

> my knees,wrists and fingers, My rheumatologist gave

> me the ususal 1

> week of steroids but did not want me to stay on them

> long term. Two

> days later the pain was back and just kept getting

> worse and worse.

> I called him twice within this week and he said to

> come in that day

> because he knows I'm usually not a complainer. When

> I saw him

> yesterday he said the RA is progressing and he wants

> me to start

> methotrexate but it would take at least 6 weeks to

> notice any

> effect. I begged (and got) prednisone for the

> meantime because I

> couldn't function. I work in a Hospital and was

> looking worse than

> half of my patients! My question is, What are the

> things I can

> expect with methotrexate? He gave me the obligatory

> speech but I

> was hoping for some people's first hand experinces.

> I took the first

> dose today, 10 mg.

>

> Thanks

>

>

>

>

>

>

>

>

Kathe in CA

__________________________________________________

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if you take mtx your will not function for a few days. i was on mtx and getting

off of it was the best thing ive done. replaced mtx with arriva and doing a lot

better.

Kathe Sabetzadeh <lv2ryd@...> wrote: Hi :

I also had to start Mtx after Plaquenil became less

effective. It took about 2 months before I started to

get benefit from it. I have been on Mtx now for about

4 years, on the pills at first, then was on Mtx

injections for a while which worked better, but am

finding it difficult to obtain injectable mtx right

now, so am back on the pills. I was up to 20 mg. a

week, but am now down to 10 mg. weekly along with

Enbrel. With the Mtx, I am more tired for the day or

two after I take it. Always take it at night, after

you have eaten, and before bed, and that way you

should be able to sleep through any nausea you might

experience. I have never had that problem. Take

Folic Acid as well, and I also take Milk Thistle to

help protect my liver. I have had some hair thinning,

and my skin is more fragile, and I am more sensitive

to the sun, since beginning the Mtx. I have had less

side effects with that than with other meds.

Otherwise, it is helping me, so I take the good with

the bad. Best of luck - and hope it helps -

Kathe in CA

--- sasupbin <sasupbin@...> wrote:

> Hi, I've been following posts on here for a while

> but this is my

> first post. I'm 39 and was dx with RA 5 yrs ago.

> Initially I took

> only NSAIDS (It took 5 different ones before I found

> Celebrex

> worked. Then fpr the past three years I was on

> PLaquenil and did OK.

> Some flare ups here and there but a week of

> prednisone would calm it

> down. A few months ago I started having pain all

> day every day in

> my knees,wrists and fingers, My rheumatologist gave

> me the ususal 1

> week of steroids but did not want me to stay on them

> long term. Two

> days later the pain was back and just kept getting

> worse and worse.

> I called him twice within this week and he said to

> come in that day

> because he knows I'm usually not a complainer. When

> I saw him

> yesterday he said the RA is progressing and he wants

> me to start

> methotrexate but it would take at least 6 weeks to

> notice any

> effect. I begged (and got) prednisone for the

> meantime because I

> couldn't function. I work in a Hospital and was

> looking worse than

> half of my patients! My question is, What are the

> things I can

> expect with methotrexate? He gave me the obligatory

> speech but I

> was hoping for some people's first hand experinces.

> I took the first

> dose today, 10 mg.

>

> Thanks

>

>

>

>

>

>

>

>

Kathe in CA

__________________________________________________

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