Guest guest Posted December 22, 2005 Report Share Posted December 22, 2005 Larry, feeling yucky for a couple days after taking MTX seems to be the norm. I took injectable MTX so those stomach and intestinal problems wouldn't be as great... ask your neuro if this is possible. After 6 weeks on the med, I feel as if the side effects are not as bad, but are still there. I say stick with it a little longer and see if things level out for you. Take care and God Bless. kerri sue Larry Brown <lbrown85@...> wrote: Hello everyone. I do not suffer from RA but I have Myasthenia Gravis. My Neuro has me on Mestinon for double vision and drooping eyes. I can't find very much about Methotrexate on the Myasthenia Group so my Neuro told me to monitor this site. I hope you don't mind. My main question is about the side effects of the medication. I am on my 4th week and will be taking 6 tablets this Sunday and that will remain my dose. I felt so bad this past Monday (nausea, diarrhea and absolute fatigue)on 5 tablets that it makes me wonder if I want to continue. How long can I expect to have the side effects? Do they last all week or just the day after the medication? After I'm on this for a while will the side effects deminish? The nurse at my Neuro's office is on methotrexate and she told me to stick with it. I've read the literature but I would like to hear from you real folks that take the medication. Any help will be appreciated. Thank You Larry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2005 Report Share Posted December 22, 2005 I've been on MTX for about a year and I still feel like I'm in a coma the day after I take it, and a little foggy the second day. After that, I'm fine. Do you have one day a week that you can afford to just sit around feeling stoned? For me, it's not an unpleasant feeling, I just can't do anything. As far as the gastro side effects, try taking it with a FULL meal -- not just a few bites of food -- with some fat in it. My doc recommended that and it really helped. If that doesn't work, and the situation doesn't improve in a few weeks, you can always have it injected. It's not the most pleasant drug to be on, but it's not the worst either. Hang in there. --- In , " Larry Brown " <lbrown85@a...> wrote: > > Hello everyone. I do not suffer from RA but I have Myasthenia > Gravis. My Neuro has me on Mestinon for double vision and drooping > eyes. I can't find very much about Methotrexate on the Myasthenia > Group so my Neuro told me to monitor this site. I hope you don't mind. > > My main question is about the side effects of the medication. I am on > my 4th week and will be taking 6 tablets this Sunday and that will > remain my dose. I felt so bad this past Monday (nausea, diarrhea and > absolute fatigue)on 5 tablets that it makes me wonder if I want to > continue. How long can I expect to have the side effects? Do they > last all week or just the day after the medication? After I'm on this > for a while will the side effects deminish? The nurse at my Neuro's > office is on methotrexate and she told me to stick with it. I've read > the literature but I would like to hear from you real folks that take > the medication. > > Any help will be appreciated. > > Thank You > > Larry > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2005 Report Share Posted December 22, 2005 Larry, Try taking it at bed so you can sleep through most of the nasuea. The fatigue and feeling pretty bad the next day or two is normal. It is a chemo. Also if your doc did not prescribe folic acid ask him about it. Most of us use it to minimize the side effects of nausea, diarrhea, mouth sores and fatigue. I was on the same dose that you are taking and did horrible..finally had to quite due to side effects. But there is another med you can ask about if the side effects get too severe. Its call Leukovorin...its a stronger form of folic acid. Good luck Toni --- In , " Larry Brown " <lbrown85@a...> wrote: > > Hello everyone. I do not suffer from RA but I have Myasthenia > Gravis. My Neuro has me on Mestinon for double vision and drooping > eyes. I can't find very much about Methotrexate on the Myasthenia > Group so my Neuro told me to monitor this site. I hope you don't mind. > > My main question is about the side effects of the medication. I am on > my 4th week and will be taking 6 tablets this Sunday and that will > remain my dose. I felt so bad this past Monday (nausea, diarrhea and > absolute fatigue)on 5 tablets that it makes me wonder if I want to > continue. How long can I expect to have the side effects? Do they > last all week or just the day after the medication? After I'm on this > for a while will the side effects deminish? The nurse at my Neuro's > office is on methotrexate and she told me to stick with it. I've read > the literature but I would like to hear from you real folks that take > the medication. > > Any help will be appreciated. > > Thank You > > Larry > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2005 Report Share Posted December 22, 2005 HI Larry, I was started on oral MTX in 1998 experimentally for my asthma. I started on 5 pills. The first few weeks, I thought I was gonna die (not really, but felt crappy) nausea, the whole bit. After about 2 months, I realized that when I took it (Monday am) ,I'd feel like crap the next day or two. It did wear off after about the second day, and after a while on it, I don't really notice any gastric problems anymore. The one side effect that has stuck with me (I am now on 8 pills a wk for the RA) is hair loss. I have long, thick hair, but lose about a handful or 2 a day when I brush it. hope this helps, Date: Thu, 22 Dec 2005 04:33:46 -0000 From: " Larry Brown " <lbrown85@...> Subject: Questions about Methotrexate Hello everyone. I do not suffer from RA but I have Myasthenia Gravis. My Neuro has me on Mestinon for double vision and drooping eyes. I can't find very much about Methotrexate on the Myasthenia Group so my Neuro told me to monitor this site. I hope you don't mind. My main question is about the side effects of the medication. I am on my 4th week and will be taking 6 tablets this Sunday and that will remain my dose. I felt so bad this past Monday (nausea, diarrhea and absolute fatigue)on 5 tablets that it makes me wonder if I want to continue. How long can I expect to have the side effects? Do they last all week or just the day after the medication? After I'm on this for a while will the side effects deminish? The nurse at my Neuro's office is on methotrexate and she told me to stick with it. I've read the literature but I would like to hear from you real folks that take the medication. Any help will be appreciated. Thank You Larry --------------------------------- Photos Ring in the New Year with Photo Calendars. Add photos, events, holidays, whatever. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2005 Report Share Posted December 22, 2005 Methotrexate severely depletes the body of folic acid. Rheumatologists usually prescribe folic acid to go along with MTX--at least 1 mg/day. If you're not taking folic acid along with the MTX it would certainly explain the problems you're having. If you are taking folic, you may need a higher dose. I struggled with fatigue at 1 mg and my rheumy upped my dose to 2-3/day. She said some of her patients take 5 mg./day. Sierra --- In , " Larry Brown " <lbrown85@a...> wrote: > > Hello everyone. I do not suffer from RA but I have Myasthenia > Gravis. My Neuro has me on Mestinon for double vision and drooping > eyes. I can't find very much about Methotrexate on the Myasthenia > Group so my Neuro told me to monitor this site. I hope you don't mind. > > My main question is about the side effects of the medication. I am on > my 4th week and will be taking 6 tablets this Sunday and that will > remain my dose. I felt so bad this past Monday (nausea, diarrhea and > absolute fatigue)on 5 tablets that it makes me wonder if I want to > continue. How long can I expect to have the side effects? Do they > last all week or just the day after the medication? After I'm on this > for a while will the side effects deminish? The nurse at my Neuro's > office is on methotrexate and she told me to stick with it. I've read > the literature but I would like to hear from you real folks that take > the medication. > > Any help will be appreciated. > > Thank You > > Larry > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2005 Report Share Posted December 23, 2005 Hi Larry, I'm assuming you meant 1 mg and not 1 mcg of folic. Yes? Sierra > > > > Hello everyone. I do not suffer from RA but I have Myasthenia > > Gravis. My Neuro has me on Mestinon for double vision and drooping > > eyes. I can't find very much about Methotrexate on the Myasthenia > > Group so my Neuro told me to monitor this site. I hope you don't > mind. > > > > My main question is about the side effects of the medication. I am > on > > my 4th week and will be taking 6 tablets this Sunday and that will > > remain my dose. I felt so bad this past Monday (nausea, diarrhea > and > > absolute fatigue)on 5 tablets that it makes me wonder if I want to > > continue. How long can I expect to have the side effects? Do they > > last all week or just the day after the medication? After I'm on > this > > for a while will the side effects deminish? The nurse at my > Neuro's > > office is on methotrexate and she told me to stick with it. I've > read > > the literature but I would like to hear from you real folks that > take > > the medication. > > > > Any help will be appreciated. > > > > Thank You > > > > Larry > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2005 Report Share Posted December 23, 2005 I don't recall if anyone mentioned that taking MTX at bedtime (with a snack) is a good idea because you can sleep through some of the side effects. Works for me. I keep water at my bedside and drink it during the night hours. Lots of water the next day, too. Sierra > > > > Hello everyone. I do not suffer from RA but I have Myasthenia > > Gravis. My Neuro has me on Mestinon for double vision and drooping > > eyes. I can't find very much about Methotrexate on the Myasthenia > > Group so my Neuro told me to monitor this site. I hope you don't > mind. > > > > My main question is about the side effects of the medication. I am > on > > my 4th week and will be taking 6 tablets this Sunday and that will > > remain my dose. I felt so bad this past Monday (nausea, diarrhea > and > > absolute fatigue)on 5 tablets that it makes me wonder if I want to > > continue. How long can I expect to have the side effects? Do they > > last all week or just the day after the medication? After I'm on > this > > for a while will the side effects deminish? The nurse at my > Neuro's > > office is on methotrexate and she told me to stick with it. I've > read > > the literature but I would like to hear from you real folks that > take > > the medication. > > > > Any help will be appreciated. > > > > Thank You > > > > Larry > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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