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 06-07-2009, 09:45 PM #11
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 Connie!

Hey hon! I am so very happy for you! I know it is awful being in the hosp, but at least they are finally listening to you! AMEN!!!!!!!!

The EMG is rather painful. I told my neuro that - he knows my fear of needles and never mentions that part until I hear him pulling on the gloves - blood everywhere - yuck! I don't mind the other part - the electic stuff going through me, but the needle still freaks me out!

Do the drs have any idea what you are allergic to? Are you feeling better @ all with the meds? How long do they plan on keeping you there?

We have missed you!!!!!
Big hugs!
Erin






Quote:
Originally Posted by ConnieS View Post
Hi all of you! Its been a bout a week since i last logged in to check this thread and gosh... 12 pages. lol... great that everyone's checking in here!

Just a quick update, i'm now in a hospital undergoing some tests, been here about a week already and having all sorts of medicine "dripped into" me. Did a emg on mon and gosh. it hurt so badly, hate the part about them digging in my flesh. Survived that test after a gruelling 1 hr odd, and am having the tensilon test later. Was told by docs today that my emg showed some abnormalities, though they didn't specify, and they mentioned that they'll have to do some more tests to be certain about my diagnosis. Its weird though, my emg in Mar showed normal results.

Am okay here, I tried walking around the day before and yesterday, and after 5 mins of walking, i slept for 3 hours. Haha! Symptoms wise, my neck's getting weaker, muscles keep twitching, and chest feels heavy.

But I'm glad the doctors here are taking my symptoms seriously, and are doing all they can to find out whats wrong with me. Am having an allergic reaction to one of the meds they gave me, so i look like a tomato now! I am also put on hormone pills and a whole lot of other pills and bags of drips for the time being.

may be having a muscle biopsy soon, anything i should take note of for that? it sounds scary.. lol.

really miss u guys. do take care alright? Have a great week everyone! will try to login when i can.
__________________
Erin
.
erinhermes 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
Part 2 of "Banned from Healthboards" thread... TireSlasher Social Chat 35 05-21-2009 08:02 AM
saving the "when did you get your initial rsd/crps dx" thread JOAN_M Reflex Sympathetic Dystrophy (RSD and CRPS) 2 09-10-2007 08:59 AM
It's July.. Mmmm, We need a "Check in Food".. dawn3063 Thoracic Outlet Syndrome 13 07-11-2007 09:06 PM


All times are GMT -5. The time now is 05:35 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.