APS, Thymoma and MG
 

Hell, I am Carrie and I was just recently diagnosed with MG. Prior to my diagnosis I have suffered with APS (antiphospholipid Antibody Syndrome). In the past year I have suffered 4 TIA's, a blood clot in my ARM, Jugular Vein and in my Kidneys all from the APS. I thought that was the root to all of my weakness and and other symptoms. In August I landed in the hospital with chest pain, shortness of breath and extreme hoarseness in my voice. It was then that they told me that I had a Thymoma and might have APS. It took 8 weeks of not having a voice and extreme weakness to get a diagnosis and to be placed on Mestinon. I was told on Tuesday that I was probably in a Myasthenic Crisis. My Myasthenia is effecting my legs, arms, eyes, and my larynx.
My question is, does any body else have a complication with MG such as APS or an other blood clotting disorder? I was told that I will need to have Trans-sternal surgery to remove my thymoma but because of my blood clots I am at a more the 50% chance of having a life-threatening heart-attack or stroke from the surgery. Oh, by the way, I am the ripe age of 29 and have two children 2.5 year old girl and a 5 year old boy.

Opps, the first word should have been Hello, not Hell. What a way to start of huh! LOL

Carrie,

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.

I am not familar with APS, Thymoma or MG, and this beeing the week-end it could be a while before someone comes in to assist you, just hang in there.

Again welcome, looking forward to seeing you around.

Darlene:hug:

Hi Carrie! Welcome aboard!!:)