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-   -   Cytoxan update - latest news (https://www.neurotalk.org/myasthenia-gravis/173685-cytoxan-update-news.html)

Juanitad 07-23-2012 05:48 PM

Cytoxan update - latest news
 
Just had my 6th treatment today and the dose has increased to the point the infusion nurses are surprised at the amount I am receiving. So far, the only side affects I have are nausea for about 3 days and medication takes care of that. The benefits have been that I am completely off Cellcept (after taking 3,000 mg/day for 12 years), my prednison is down to 7 mg/day (headed slowly to zero) and my mestinon usage is down to 1 or 2 pills a day (from 6/day). So far, the benefits have far outweighted the side affects. FYI, I am also stretching my IVIG from every 2 weeks to 3 weeks.

Aside from the mediation reduction, I am feeling better also. I have more energy overall and everyone says my face is more alive and mobile.

Doc is not sure if we will do another treatment in 4 weeks, but I have an appointment for a checkup anyway. The original study did 6 treatments monthly, then bi-monthly for 6 more months. Just have to wait and see what happens.

So far, so good!

scrubbs 07-24-2012 11:29 AM

What do you mean by mediation reduction or did you mean medication reduction?

scrubbs

Juanitad 07-24-2012 10:22 PM

Sorry! Meant medication reduction - don't know how the mediation would work???

motorcycle diva 07-30-2012 12:03 AM

Great news for you! I pray this positive reaction to the drug will continue. Keep us informed. At this time, I am taking Immuran only. I am controlled at this time but you never know when it will wake up and disrupt your life!

Quote:

Originally Posted by Juanitad (Post 900010)
Just had my 6th treatment today and the dose has increased to the point the infusion nurses are surprised at the amount I am receiving. So far, the only side affects I have are nausea for about 3 days and medication takes care of that. The benefits have been that I am completely off Cellcept (after taking 3,000 mg/day for 12 years), my prednison is down to 7 mg/day (headed slowly to zero) and my mestinon usage is down to 1 or 2 pills a day (from 6/day). So far, the benefits have far outweighted the side affects. FYI, I am also stretching my IVIG from every 2 weeks to 3 weeks.

Aside from the mediation reduction, I am feeling better also. I have more energy overall and everyone says my face is more alive and mobile.

Doc is not sure if we will do another treatment in 4 weeks, but I have an appointment for a checkup anyway. The original study did 6 treatments monthly, then bi-monthly for 6 more months. Just have to wait and see what happens.

So far, so good!


suev 07-30-2012 06:05 PM

Terrific! Really hope the improvement continues to get even better and better!!


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