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

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 02-06-2016, 11:06 AM #1
simplelife15 simplelife15 is offline
Junior Member
 
Join Date: Sep 2013
Posts: 16
10 yr Member
simplelife15 simplelife15 is offline
Junior Member
 
Join Date: Sep 2013
Posts: 16
10 yr Member
Default Thoughts?

Hi all! It's been awhile, but since more heads are better than one sometimes...

Had my thymectomy in Aug. 2014. At the time I was on Prednisone, taking up to 1000 mg of Mestinon per day, and ended up on IVIG.

Within weeks of the thymectomy saw drastic changes, with a continuous gradual drop in Mestinon use and was able after about 9 months to completely stop the Prednisone.

As of the end of this past November I became completely medication free. At worst I had very mild transient symptoms that were never bad enough to need anything. Until about 10 days ago and everything came back...generalized weakness in my limbs, shortness of breath, etc. Started with 30 mg of Mestinon the first couple of days when the SOB would start to act up, now up to 120 mg/day.

Was scheduled to see my neuro for a 6 month f/u in April, which is now moved up to this coming Tuesday. His immediate recommendation is to restart Prednisone...which is where you guys come in.

When I was on the Prednisone the anger & agitation were HORRIBLE. I have two young children and my patience for them was suffering, which means they were too. My husband tolerated it, but once I weaned off he was honest about how bad it was, and it was pretty darn bad.

So, I'm reluctant to go back on it. My thoughts: this could be a temporary flare-up that could calm down on it's own and I can manage the symptoms with Mestinon in the meantime. I also know the Prednisone can make things worse before they get better; so if I start the Prednisone and that is the case what if it turns a temporary flare into something more until it kicks in and then I have to go through the weaning/withdrawal process again?

Am I making a poor choice to not follow doctors orders, or do I have good arguments for taking a wait-and-see approach? I just wish I knew if this was the start of another long-term/permanent bout with symptoms, or a short-term flare-up.

Thoughts anyone? Please and thank you!
simplelife15 is offline   Reply With QuoteReply With Quote
 


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
I would appreciate your thoughts on this Lynn Multiple Sclerosis 4 09-14-2011 04:12 AM
some thoughts... alice md Myasthenia Gravis 1 08-16-2011 04:47 AM
Thoughts About PT pht56 Traumatic Brain Injury and Post Concussion Syndrome 7 06-26-2009 06:19 PM
Your Thoughts Please sadeyesr4ever Survivors of Suicide 4 02-21-2007 09:36 AM


All times are GMT -5. The time now is 01:47 AM.


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.