Tomorrow is officially National Multiple System Atrophy, (M.S.A.) It is a day to make others aware of this rare illness. To help the ill and families get the word out that WE want and WE NEED a cure.
We all know that most likely Al won’t be able to be helped by a cure, BUT we can be very involved. We can help others not to suffer like Al has. Me as his sister and caregiver, the M.S.A. support groups, my friends here and on Face Book; everyone is doing their part to get the word out.
Since Al won’t be able to go to Day Program tomorrow on the day of awareness he and I decided to start today. He wasn’t feeling well this morning so his photo was not taken in his purple shirt. I did my hair and am wearing purple.
I am asking all of you to go to the M.S.A. site https://www.facebook.com/Miracles.for.MSA and light a candle. There is a section there to place Al’s name. If you want to donate to M.S.A. in honor of Al or someone you know with this terrible disease, please do, but no pressure from me.
So here it is, our day here, starting today helping make everyone aware of M.S.A.
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Terry, I tried to go to the site and I got a message that it wasn’t available?
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https://www.facebook.com/Miracles.for.MSA
I tried it out and this worked. Hope it works for you
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Terry your top link doesn’t work, but the one in your comments does, thanks!
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I saw that. I don’t know what happened but I am glad the one below works. Thanks for the tip my friend
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I hope I fixed it!
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Lovely…hope it’s a huge success! You go girl!!!!!!!!
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thanks Dianne. I want to save someone else who has this so they don’t have to go through the hell Al does
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way to go Terry…going to try and check out the site!
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if for some odd reason the link in the post doesn’t work, the one in the comment section does. Thanks Marilyn!
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*hugs*
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hugs
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Sure will go and light a candle.
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thank you so much Digital!!! I appreciate you and here’s a hug for you. huggggggggggg!
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