Quote:
Originally Posted by crayolagal
Greetings all...
I was recently diagnosed (June 2013) with a positive antibody test and SFEMG. My first symptoms were a droopy eyelid and double-vision (May 2013). My current MG symptoms are ptosis, double-vision, face droop, some fatigue, and little swallowing issues. I'm taking daily Mestinon (60mg x 3) and Prednisone(10mg dose) and feeling fine for the most part.
I know that I am very fortunate to have been able to get diagnosed and tested this quickly. I've been seeing an Neurologist who has a specialty in MG and he fits me in to the MDA clinic for appointments. I just turned 41 and he recommends a Thymectomy (VATS method). My thymus is "normal" - no thymoma present in the CT but both he and the Thoracic Surgeon (who I saw today) recommend the procedure.
This is just moving so quickly and it is freaking me out ![EEK!](images/smilies/eek.gif) They want to get me prepped for surgery with plasmapheresis or IVIg shortly after my family vacation in August.
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So how did the surgery go? I'm similar in age as you and also have no thymoma. I just spent 7 days in the ICU and received 5 days of IVIG and am getting ready to start biweekly IVIG treatments this week.
I'm doing much better now with some occasional double vision, speaking and swallowing problems, and a droopy lid once in a while.
My neuro has me seeing another neuro next week for a second opinion who he believes will agree that a thymectomy is the best option long term with IVIG, mestinon, prednisone, and maybe cyclosporine in place of prednisone since I haven't responded to the prednisone as I ready for the surgery.