NeuroTalk Support Groups - new member alan

NeuroTalk Support Groups (https://www.neurotalk.org/)

- New Member Introductions (https://www.neurotalk.org/new-member-introductions/)

- - new member alan (https://www.neurotalk.org/new-member-introductions/55778-alan.html)

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 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.

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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hello allen ... welcome to neurotalk

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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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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 :hug:

Hi Alan and Welcome to NeuroTalk. I'm glad you found us. If you need any help navigating just ask.

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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.

myathenia gravis

Quote:

Originally Posted by alan53 (Post 384008)

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.

Just wanted to add my welcome Alan....:welcome_sign:
So glad you stumbled upon us...great folks hanging around...my best friends!:hug:
Take care and hope to get to know you better!

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