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Old 10-07-2008, 12:13 PM #1
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Smirk new member alan
hi when you think your alone and no one understands what your going thro its a GREAT SUPRISE TO FIND THIS PLACE. MY NAME IS ALAN IM 55 AND AFTER 10 MONTHS IVE JUST BEEN DIAGNOSED WITH MYATHENIA GRAVIS DOUBLE VISION AND TIREDNESS.
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Old 10-07-2008, 12:30 PM #2
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Hi Alan! Sorry for your diagnosis, but glad you found us.

You'll like it here, I'm sure. There are lots of friendly and helpful folks.
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Old 10-07-2008, 02:43 PM #3
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Hi Allen and welcome to NeuroTalk! I'm so glad you found the site and joined us. I've posted the link to the MG forum in case you haven't visited it yet. Feel free to join in anywhere....everyone here is very friendly and supportive.


http://neurotalk.psychcentral.com/forum77.html




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Old 10-07-2008, 05:47 PM #4
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hello allen ... welcome to neurotalk
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Old 10-07-2008, 08:24 PM #5
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Hello Alan and welcome to Neuro talk, follow that link and explore ask and answer questions, and do not hesitating to explore all of Neuro talk there are many fun and helpful forums, again welcome to NT
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Old 10-08-2008, 01:39 AM #6
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Alan,

Hello and welcome to NeuroTalk. Great to see you have come to be with us. Just let us know if we can be of any help.

Again welcome, looking forward to seeing you around.

Darlene
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Old 10-08-2008, 01:55 PM #7
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Hi Alan and Welcome to NeuroTalk. I'm glad you found us. If you need any help navigating just ask.

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Old 10-09-2008, 10:54 AM #8
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a big thankq for the nice welcomes. this is like learning to ride a bike without the many falls.never been in to using computers, and like most people here have questions.
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Old 05-24-2011, 03:21 PM #9
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Default myathenia gravis
Quote:
Originally Posted by alan53 View Post
hi when you think your alone and no one understands what your going thro its a GREAT SUPRISE TO FIND THIS PLACE. MY NAME IS ALAN IM 55 AND AFTER 10 MONTHS IVE JUST BEEN DIAGNOSED WITH MYATHENIA GRAVIS DOUBLE VISION AND TIREDNESS.
Hi there. I also have myathenia gravis, I just recently got diagnosed several months ago, although I think I've had it at least 5 years. It's a terrible disease with a lot a symptoms. I just started taking the mestinon but I have been feeling very weak and dizzy. My pulse is also slower than usual and I think the side effects are getting to me. I really don't know what to expect from this disease and I am getting really scared. It took them 2 years to diagnose it, major problems with swallowing and slurring my words. I had problems with attacks where my arms would got limp and searing pain through them at the same time. I am very happy to have found this site and I hope to hear back from you about your experience with this wonderful disease, smiles.. Take care Darlene.
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Old 05-24-2011, 09:30 PM #10
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Just wanted to add my welcome Alan....
So glad you stumbled upon us...great folks hanging around...my best friends!
Take care and hope to get to know you better!


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