Myasthenia Gravis Support Group
Myasthenia gravis (MG) is a neuromuscular disease leading to fluctuating muscle weakness and fatiguability. The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and...
I joined the group when TJ and Curt would have quite the heated discussions. Miss those debates !!! Of course we all miss Curt !!!
And TJ, even though Curt didn't like all the research links you posted, we all learned a lot form both of you !!!!
Great idea Kimber!! I can honestly say positive thoughts and determination have helped me be symptom free !!!
Robin
Of course I wish everyone the best.
Some people that I want to be better very soon and I would like to send good thoughts to are Curt, Annette, Marvin, Debbie, Cathi, Marty, Dean, Steve, Ross...In no particular order.
The best of thoughts for the best strength possible.
Love,
TJ
can not do it alone anymore when I still can not make my walk around the block...
Dean
Dean
I am sorry you are having a tough (under statement) time. Make yourself believe the answers are coming. Belief can be just as important as medication. Try to find something positive each day. Even if it is small. Embrace it. Let that feeling fill you. Use it. Enjoy it. MG may take control of our bodies but it cannot control our feelings unless we let it. It cannot take my joy. It can make it harder to find but it cannot take it.
I wish I had a picture of a rose to send you.
My most positive thoughts go out to you.
Kimber
I think I told you about Curt, and what a difference his kick-ass attitude had for me. You could be macho, and have MG, and just treat it like another obsticle -- Nora Ephron would say "above all, be the heroine (or hero) of your life, never the victim."
Lots of people first come on this site and have just been diagnosed, or have almost been diagnosed, or are waiting. They do frantic googling, and they feel guilty, because this disease makes you lazy, and there must be a reason. Perhaps we did something in our past that we are paying for now? Perhaps if I just cut XXXX out of my diet I will be all fine and dandy again! This site, and all my fellow sufferers who write about their lives here, make the whole concept of having MG more manageable. Less scary. Reducing stress I would otherside give myself by frantic googling!
I would be remiss if I didn't make special mention of Rev. Dr. Kerry Bunn. I watched his videos with one heavily-lidded eye during my diagnosis, and they made a difference. His pre- and post-mestinon sit-ups were inspirational, and I fully intend to get around to doing one of them one of these days.
Right now I will just "chill" and hope all of you can too...
~joe
Send your thoughts to Lorraine, Jeannie and Kerry as well!
We all could just use a BIG BOOST of luck. CMON GIVE IT TO US
Sending you strength,
Gail
You guys are the best. It can be a lonely and frightening thing to live with mg. I can't imagine not having my mg brothers and sisters. Even when I am quiet I know you guys are here and I am not alone.
Dean, God bless you and your upcoming appointment. Know the room will be crowded because we are all there with you. You may have to tell us to hush so you can get some rest. ;-)
Love you all,
Cathi