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

Reply
 
Thread Tools Display Modes
Old 09-20-2009, 12:46 PM #1
erinhermes's Avatar
erinhermes erinhermes is offline
Senior Member
 
Join Date: Jul 2008
Location: San Antonio
Posts: 1,471
15 yr Member
erinhermes erinhermes is offline
Senior Member
erinhermes's Avatar
 
Join Date: Jul 2008
Location: San Antonio
Posts: 1,471
15 yr Member
Heart Hi Shari!

Forgot something......the pred made me feel better IMMEDIATELY! Granted it was prolly b/c I was also receiving MASSIVE amounts of IV IG and fluids, but really and truly the very next day my speech problems were gone! *poof*!

Hope this finds you strong and happy!

Love,
Erin






Quote:
Originally Posted by Shari_W View Post
Thanks Lizzie,
Everything you mentioned is the reason why I am trying to do everything in my power not to begin prednisone therapy. I tend to have a bad MG flare up every four years or so but am really baffled as to why I had this one considering that my treatment plan for MG for the past 4 years has been pretty aggressive. We have increased my cellcept dosage from 2000 mg to 2500 mg daily and now have bumped my IVIG back to once a month instead of every 6 weeks. I also have increased my mestinon dosage a little as well.
It's been a couple of months now since my MG symptoms have come back and they are still hanging around so I guess I am just a little impatient about getting them under control again I tried a different IVIG brand the last couple of times and I am going back to the one I had before. The new brand left me feeling worse with side effects than my old one and it doesn't apppear to be giving me the benefits that I used to get. But prednisone really scares me because of everything you said.

I can say this, the intensity of my weakness is not nearly as bad as it was a couple of months ago so maybe I just need to relax and not worry about it so much. My husband keeps telling me to take it one day at a time as I have done in the past. I guess I just got spoiled to feeling "normal" for so long that it is hard for me to adjust to feeling like this again. I am still not as bad as many others who post on here so I am really thinking long and hard about the prednisone therapy.

I just want to get back to being able to do things with my husband and kids instead of being afraid to do anything because it might make my MG worse. I am not living right now, just merely existing.
__________________
Erin
.
erinhermes 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


Similar Threads
Thread Thread Starter Forum Replies Last Post
Parkinson's and Prednisone AnnT2 Parkinson's Disease 9 09-24-2018 02:38 PM
Prednisone Maxwell'sMom Myasthenia Gravis 22 11-09-2009 09:09 AM
Prednisone bobber Reflex Sympathetic Dystrophy (RSD and CRPS) 17 06-28-2009 04:23 PM
Prednisone slskckjebw Multiple Sclerosis 5 05-08-2009 11:20 PM
Prednisone HeyJoe Medications & Treatments 6 10-28-2007 06:03 PM


All times are GMT -5. The time now is 07:37 PM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 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.