Which ideas are best for promoting our drive to put MG on the map? Choose as many as you like, from the ideas below

1 Comment

  • Debbie Brogdon - 13 years ago

    We need more local support groups. I live too far from one and trying to start one in my local hospital but meeting a lot of resistance. Healthcare workers do not understand MG, the medications I take, nor the rest that is needed. Mestinon is a blessing for me to be able to chew and swallow but when I have to go to the hospital, they do not understand that I need it prior to eating so I can chew and swallow.

    Articles regarding MG need to go into newspapers so others understand what it is and why some people have slurred speech. I have teased and just say that I had too much alcohol to drink.

    My vision has been affected and providing large font helps so much when I am not too tired and then the double vision kicks in. Luckily, I have a good doctor that added prism to my glasses and this has been a blessing.

    Support is crucial and if others don't understand, how can they help? More information on MG needs to get to medical staff and people in the community.

    Thank you for listening and maybe there will be a cure one day. :-)

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