WOW thats quite a load of heavy-duty meds for your daughter. How old is she?

My 1st rheumy put me on Methotrexate treating me for the differential of sjogren's a mimic of MS. It made me tired and kinda sick, not bad but I just didnt want to do anything for the weekend I took it. I only needed to take it once a week. So.. I eventually got off. Besides you have to have blood draws each time you see the Rheumy to check for toxic levels.

BUT.. while getting off of it ( I was weaned) I noticed that for the first time my leg muscles were not hard and tight from the spasticity. I guess it helped and I didnt notice it.

My 2nd Rheumy (the first one moved) didnt agree with her DX anyhoo... so I would not be on anything. Geez

Good luck but I would weigh this one out if this is a child.

Nice to SEE you my dear

Warmly Jan

I was on methotrexate shots for about a year in combination with Betaseron to treat my MS. I titrated up from .4 cc to 1 cc over a period of 4 months and was sick each week the day of the shot. Flu-like symptoms and then each titration I was sicker...

The purpose of the MTX was to break the exacerbation cycle I was in. I was having exacerbations every 3 months. After the year, it didn't work and I was so sick that the rheumy that was monitoring me decided that it just wasn't worth it. My white count was hovering at the low normal level and my platelet count had started to decrease.

They also had me take folic acid along with the MTX.

I know that there are a lot of people who take MTX for MS therapy and have had good luck with it...I just wasn't one of those people...I happen to be one of those med sensitive people.

I think Kinch52 takes it...and you might want to post something on the medications forum asking about it as well.