Neurally Mediated Syncopy
 

Hello everyone, my name is Myra and I'm from Bennettsville, SC. I was diagnosed with NMS 2 years ago and recently diagnosed with fibromyagia. I have not been able to work for months now and I was wondering if anyone out there with NMS has had any experience with filing for disability benefits. I have hoped to return to work but that isn't looking to promising.
Things have really been difficult in every aspect of my life. I could use some support.
Thanks!

Myra,

Hello and welcome to NeuroTalk. Great to see you have come to be with us. You will find a great number of caring, supporting members here willing to help each other as they can.

Here is the link to Fibromayagia:

http://neurotalk.psychcentral.com/forumdisplay.php?f=12

Again welcome, looking forward to seeing you around.

Darlene:hug:

Hi Myra and Welcome! I feel your pain..literally. I have FM and it's one of the reasons I had to leave my employment. I do not recieve, nor have I ever applied for disability. I have a few other DX"s on my plate, but am fortunate in that my DH works.

I'm glad you found us and look forward to hearing more from you. take care. :welcome_sign:

Hi, Myra! :Wave-Hello: Welcome to NeuroTalk!