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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#1 | ||
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New Member
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I am new to this forum. I have MG, small fiber neuropathy, autonomic neuropathy, etc. Most of my posting has been on other sites. Though our symptoms may differ, we all share this horrible disease.
I know we all go through some very difficult times and circumstances. I have also observed a sense of "thankfulness" among people who experience suffering. That spirit of thankfulness seems to encourage others. Since Thanksgiving is next week, would anyone like to share what they are thankful for? *edit* Last edited by Chemar; 11-20-2010 at 08:26 AM. Reason: NeuroTalk guidelines |
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#2 | ||
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Grand Magnate
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Well, Krbunn, I'm thankful when people respond to posts, especially from new posters!
![]() Frankly, I'm simply grateful one foot still goes in front of the other. Have a good Thanksgiving. Annie |
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"Thanks for this!" says: | craftyRCC (11-22-2010) |
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#3 | ||
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Member
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I'm grateful that Mestinon allows me to sleep and wake up in the morning breathing.
I'm grateful the doctor is willing to continue Mestinon for me, even though he is not 100% on board with me having MG. |
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#4 | ||
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Junior Member
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After reading some of the recent horror stories here, I have to say I am thankful for my Neurologist. He ROCKS. Although I am not yet diagnosed, he ran me through the obvious tests and when they came back inconclusive, his reaction was that HE must have done something wrong in the EMG testing and is sending me to a specialist in Indy. Still waiting for the date for the appointment, but I am ready.
I am also thankful for an advanced degree in Biology. Although it is not my profession and I have not used it in over a decade, it makes it much easier for me to read and understand research papers and be an informed advocate for myself. |
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#5 | ||
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Member
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Welcome to the board Dr. Bunn!
I know I've already answered your question on the other forum I'll answer again for those who don't visit the Daily Strength forum. I am thankful for my family and friends, they have been my rock during this crazy time in my life. Without them some tasks would be nearly impossible. For my neurologist, in the begining some of my symptoms seemed kind of vague to me, he started testing me for MG right away. It was so nice to have someone listen and not look at me like I have two heads! Whether this turns out to be MG or not. I'm very thankful for all the new friends I've made on this and the other MG forums I follow. Everyone is so kind, caring, and helpful.. It's great to have a place to share what's happening to you with others who understand what you're going through. (Sometimes I wish we all lived down the road or around the corner though, it be great to meet face to face over a cup of coffee or something) I am most thankful to God for each and everyday I have to spend with my family and friends. Some days are good, some bad. But I am extremely grateful for each and every day! I feel each one is a gift to be cherished! Wishing you and your a Happy Thanskgiving, Rachel
__________________
You never know how STRONG you are, until being STRONG is the only choice you have!
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#6 | ||
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Member
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I still suffer symptoms of MG like general weekness, pain throughout my body when I am on my feet for any length of time, good and bad days of fatigue but compared to last year I am grateful for:
Being able to take a shower without stopping to rest anymore. Not having to live with double vision. I can chew and swallow fine again. Getting in and out of the car is not a major chore anymore. I remind myself mentally of these things every day. Happy Thanksgiving to all. Tony. |
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