New Member Introductions Welcome to our community! Come in and introduce yourself to other members!!


advertisement
Reply
 
Thread Tools Display Modes
Old 02-20-2013, 08:17 PM #1
Interested Interested is offline
Junior Member
 
Join Date: Feb 2013
Posts: 31
10 yr Member
Interested Interested is offline
Junior Member
 
Join Date: Feb 2013
Posts: 31
10 yr Member
Default New to Myasthenia Gravis and Neuro Talk

Hi, I recently joined this group and am trying to figure out how to navigate this site. My forty year old son was diagnosed with MG in October, 2012 via eye muscle tests, blood tests, and a CT. In December he had a thymectomy and had a thymoma removed. He does not need chemo or radiation, but needs to get a CT every six months. He is now on 60 mg of Mestinon three times daily, and 20 mg of Prednisone twice daily. The neurologist said he would probably have to adjust his dosage when he goes to back to see him the end of this week.

His ptosis and double vision have subsided. However, he now has problems chewing, feels like he has rubber bands in his mouth, sometimes has problems getting words out when preaching, and has weakness in his arms and legs. He also notices that he feels like he doesn't have enough air when he tries to sing and can't whistle. I know the neuro doc is still trying to find the proper doses of medicine, but he worries his neurologist may not be agressive enough.

My son has a very busy schedule and doesn't have time to join communities such as this one. Actually, I think he is just too exhausted to do much once he gets home. Consequently, he asked me to check things out for him because I am retired. Since I am also very concerned about his condition and what may lie ahead, we are both hoping that we might find some pearls of wisdom from this site.

Some of his questions include asking people if they could offer advice as to helpful things they wish they would have known when they were first diagnosed, whether there is a special diet that could help, if certain exercises are helpful, and what should he be asking his neurologist, also, are there any tips that would enable him to prevent fatigue.

We never heard of MG before October, but it certainly seems to be a disease that encompasses your entire life. Any advice would be greatly appreciated.

Thanks,
Interested
Interested is offline   Reply With QuoteReply With Quote

advertisement
Old 02-21-2013, 01:33 AM #2
Darlene's Avatar
Darlene Darlene is offline
Legendary
 
Join Date: Sep 2006
Location: Once a Texan, always a Texan.
Posts: 11,976
15 yr Member
Darlene Darlene is offline
Legendary
Darlene's Avatar
 
Join Date: Sep 2006
Location: Once a Texan, always a Texan.
Posts: 11,976
15 yr Member
Wink Great to meet you!!


Interested,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. You will find out we are supportive and relaxing place.

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.
__________________

.

"Life without God is like an unsharpened pencil -- it has no point.
Darlene is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Interested (02-21-2013)
Old 02-21-2013, 03:36 PM #3
Interested Interested is offline
Junior Member
 
Join Date: Feb 2013
Posts: 31
10 yr Member
Interested Interested is offline
Junior Member
 
Join Date: Feb 2013
Posts: 31
10 yr Member
Default

Quote:
Originally Posted by Darlene View Post

Interested,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. You will find out we are supportive and relaxing place.

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.
Thanks for the prayers, Darlene! I do believe that the Lord is still the Great Physician! Am looking forward to reading the posts on this site. Praying for you also, Darlene.

Interested
Interested is offline   Reply With QuoteReply With Quote
Old 02-23-2013, 10:43 PM #4
SRL1 SRL1 is offline
New Member
 
Join Date: Feb 2013
Posts: 2
10 yr Member
SRL1 SRL1 is offline
New Member
 
Join Date: Feb 2013
Posts: 2
10 yr Member
Default

Quote:
Originally Posted by Interested View Post
Hi, I recently joined this group and am trying to figure out how to navigate this site. My forty year old son was diagnosed with MG in October, 2012 via eye muscle tests, blood tests, and a CT. In December he had a thymectomy and had a thymoma removed. He does not need chemo or radiation, but needs to get a CT every six months. He is now on 60 mg of Mestinon three times daily, and 20 mg of Prednisone twice daily. The neurologist said he would probably have to adjust his dosage when he goes to back to see him the end of this week.

His ptosis and double vision have subsided. However, he now has problems chewing, feels like he has rubber bands in his mouth, sometimes has problems getting words out when preaching, and has weakness in his arms and legs. He also notices that he feels like he doesn't have enough air when he tries to sing and can't whistle. I know the neuro doc is still trying to find the proper doses of medicine, but he worries his neurologist may not be agressive enough.

My son has a very busy schedule and doesn't have time to join communities such as this one. Actually, I think he is just too exhausted to do much once he gets home. Consequently, he asked me to check things out for him because I am retired. Since I am also very concerned about his condition and what may lie ahead, we are both hoping that we might find some pearls of wisdom from this site.

Some of his questions include asking people if they could offer advice as to helpful things they wish they would have known when they were first diagnosed, whether there is a special diet that could help, if certain exercises are helpful, and what should he be asking his neurologist, also, are there any tips that would enable him to prevent fatigue.

We never heard of MG before October, but it certainly seems to be a disease that encompasses your entire life. Any advice would be greatly appreciated.

Thanks,
Interested
My experiance is no matter what combination of meds he is taking he will need to slow down and reduce stress in his life. it has been difficult for me, I still struggle my brain thinks i am superman but my body cannot keep up. I have slowly reduced my stress and my symtoms have improved. good luck.
SRL1 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Interested (02-26-2013)
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
Myasthenia Gravis bobcatsrule Myasthenia Gravis 8 07-07-2013 09:09 PM
Myasthenia gravis and MS? jacksonsmommy Multiple Sclerosis 1 01-30-2013 05:46 PM
Myasthenia Gravis Janla New Member Introductions 3 08-16-2012 06:57 PM
Myasthenia Gravis-Neuro Appointment Today Kathie Glenn Myasthenia Gravis 10 05-03-2010 12:18 PM
Myasthenia Gravis bobcatsrule New Member Introductions 5 01-07-2008 10:48 AM


All times are GMT -5. The time now is 03:35 AM.

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.