Member
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Join Date: Jul 2010
Location: Live in upper midwest
Posts: 439
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Member
Join Date: Jul 2010
Location: Live in upper midwest
Posts: 439
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You are a very kind and caring daughter. My daughters who are 40 and 33 have really struggled with my MG, health that degraded slowly at first but over past 3 years fast. My youngest still is trying to be in as much denial as possible. In her defense she as an extra child and was in the middle of her last birth and a hysterctomy when it hit 3 years ago. She also has a siezure disorder so she has to keep her stress level down. It has all been very had on our little family. I am glad you stopped her for information. I always feel better with as much information as I can get. I know too that I wish the girls just would call more often. It is lonely being homebound. I used to work for a call in crisis line. Until you really need it yourself it is hard to understand how very much just being listened to helps, even heals.
Annie59
[QUOTE=jwaters15;755961]Hello to all. I am writing this for my dad. He has been diagnosed for a little over a year with MG, but he has had symptoms for much longer. I would like to share some of his story in hopes that someone has experienced similar things and maybe have some answers.
Last Feb. we were told that my dad has ALS.
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