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


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 09-01-2010, 07:33 AM #1
rach73 rach73 is offline
Member
 
Join Date: Apr 2009
Location: Devon, United Kingdom
Posts: 531
15 yr Member
rach73 rach73 is offline
Member
 
Join Date: Apr 2009
Location: Devon, United Kingdom
Posts: 531
15 yr Member
Default Update on me

Hi everyone,

I just thought I would update you all with what has been going on with me as I haven't been on for months and months - well it seems like that.

Also welcome to all the newbies and I hope that you are managing to get answers to your questions.

I have been very poorly and been in bed a lot of the time. Unfortunately it seems I have developed a new condition on top of all the other poo I have to deal with!

I have been suffering with constant nausea, vomiting and stomach pains for around a year. In June I was hospitalised as my abdomen swelled so much I looked like I was 9 months pregnant. Since then I have been pretty much on a daily diet of morphine and tramadol.

I saw a consultant surgeon in August and after actually listening to me ( the first Dr in a long time) he believes I have gastroparesis - paralysis of the stomach / stomach doesn't work properly. I am vomiting undigested food from meals I have eaten 9 hours earlier ( sorry to be graphic) I am rarely hungry and somedays I can't even process liquids.

The consultant I saw believes that the gastroparesis is another symptom of this undiagnosed neurological condition that I have. Symptoms include plummeting blood pressure, blood pooling, breathing problems, weakness, fatigue, facial weakness, swallowing problems , ptosis. Maybe this is a weird presentation of MG or a totally new neurological illness that I have. As this guy I have seen is a surgeon I wont be seeing him again as I dont need an operation. I am currently waiting to see the gastro team.

I have spent weeks in bed with nausea, vomiting and pain.

For some good news I have resolved the issue with my numb feet and hands I had low b12 serum levels - 178, the cut off is 180 in the UK and it has been a battle to get treatment. Within 5 days the numbness went from my feet , mentally I felt a lot clearer and I only get numb hands/ fingers about once a week now. I opted for tablets rather than injections as I had some injections recently and the site was painful for weeks afterwards. Having got much worse sickness wise its a battle to get the darn things down and stay down!

Im really sorry its been so long since I have been on but I really have been awful. I just hapen to be having a reasonable day where I am only facing the battle of not vomiting, not swelling and pain.

Has anyone else on here developed gastroparesis?

Thanks
Love
Rach
rach73 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
Another update tysondouglass Myasthenia Gravis 9 12-04-2009 12:02 PM
update on my dad!! sabimax The Stumble Inn 14 02-10-2009 01:28 PM
update Melina Trigeminal Neuralgia 8 06-12-2008 08:55 AM
My Update buckwheat Thoracic Outlet Syndrome 14 03-08-2007 05:35 PM
Update colombiangirl1 Schizophrenia 0 02-26-2007 04:17 PM


All times are GMT -5. The time now is 08:51 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.