Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS.


advertisement
Reply
 
Thread Tools Display Modes
Old 10-16-2014, 09:49 PM #1
huntress huntress is offline
Member
 
Join Date: Jul 2012
Posts: 104
10 yr Member
huntress huntress is offline
Member
 
Join Date: Jul 2012
Posts: 104
10 yr Member
Default Cyclosporin

Hi all. Well neuro believes Rituxan did little for me. He is taking me off azathioprine which it has been 15 months for me and its not working. So he has me starting 200mg Cyclosporin. Dropping azathioprine cold turkey. Anyone take cyclosporin and thing I am worried about. Swollen gums what are your experiences with it? Thanks.
huntress is offline   Reply With QuoteReply With Quote

advertisement
Old 10-16-2014, 11:02 PM #2
catie catie is offline
Junior Member
 
Join Date: Feb 2010
Posts: 99
10 yr Member
catie catie is offline
Junior Member
 
Join Date: Feb 2010
Posts: 99
10 yr Member
Default

Quote:
Originally Posted by huntress View Post
Hi all. Well neuro believes Rituxan did little for me. He is taking me off azathioprine which it has been 15 months for me and its not working. So he has me starting 200mg Cyclosporin. Dropping azathioprine cold turkey. Anyone take cyclosporin and thing I am worried about. Swollen gums what are your experiences with it? Thanks.
Hi,
I've been on Cyclosporine for about 2 1/2 years. It's kept my symptoms to a minimum except for my double vision. I did much better with prednisone added to my cyclosporine, but was successfully weaned off of pred in March and don't really want to go back on it, so I just deal with a few more symptoms.

Blood levels should be checked at least monthly and more often when you first start on Cyclo. It's important for the neuro to especially monitor your kidney function and blood pressure as Cyclosporine has been known to adversely affect both.

I have not had any problems with swollen gums but the list of side effects is long. In fact, my neuro said that Cyclosporine is usually tried after other medication options have been exhausted since there are a lot of side effects and lab values have to be monitored so closely.

I hope you have some success with the Cyclosporine. It sounds like you have been on a few other drugs without much success.

Cate
catie is offline   Reply With QuoteReply With Quote
Old 10-19-2014, 10:40 PM #3
AnnieB3 AnnieB3 is offline
Grand Magnate
 
Join Date: Feb 2009
Posts: 3,306
15 yr Member
AnnieB3 AnnieB3 is offline
Grand Magnate
 
Join Date: Feb 2009
Posts: 3,306
15 yr Member
Default

I haven't had experience with it, but I wanted to wish you well. Make sure you discuss your concerns with both your neuro and internist (who can do those blood tests to check on your immune system and liver/kidneys).

Annie
AnnieB3 is offline   Reply With QuoteReply With Quote
Old 10-20-2014, 07:02 PM #4
huntress huntress is offline
Member
 
Join Date: Jul 2012
Posts: 104
10 yr Member
huntress huntress is offline
Member
 
Join Date: Jul 2012
Posts: 104
10 yr Member
Default

Thanks. I start them tomorrow. Hoping for good results. Will keep updating on any side effects or such. If this doesn't help thmectomy is next.
huntress is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off



All times are GMT -5. The time now is 10:13 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.