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Related: Editorials & Other Articles, Issue Forums, Alliance Forums, Region Forumsso, i've never made any kind of beg here for myself. this isn't rly 1 either, but it is. updated.
Last edited Fri Apr 19, 2024, 08:07 AM - Edit history (2)
i will b doing the mswalk may 19th, in northbrook, il.
if u r inclined to help, pls go read my pitch.
https://events.nationalmssociety.org/participant/525188
ok, eta my pitch-
im walking toward a world free of ms
because this cruel disease stole my sister.
my sister patty passed away in 2018 after a decade in a nursing home, and a life under its shadow. dxd after the birth of her 2nd child, she thankfully spent most of the next 20+ yrs in remission. but she never had another child. she dared not try to combine work and motherhood. and when she returned to the workforce once her son was an adult, it reared its ugly head. it took about a decade to fully disable her. it took a toll not only on her body, but her brain. her initial admissions to care were in the locked ward.
i walk w my dearest of friends, roberta miles, because she too lives in the shadow of this beast. but she does it with a style and grace that mostly able bodied me can only dream of. she sings, she tells stories, she makes art, she teaches, she produces several long running shows, including loose chicks monologue group. i had the pleasure of making my debut as a storyteller w the chicks at my urban farm, moahs ark.
fortunately, roberta has had access to treatments that did not exist when my sister could have benefited from them. but she still struggles.
i want a world free of ms for her, and for every one who has to face this cruel killer.
because this cruel disease stole my sister.
my sister patty passed away in 2018 after a decade in a nursing home, and a life under its shadow. dxd after the birth of her 2nd child, she thankfully spent most of the next 20+ yrs in remission. but she never had another child. she dared not try to combine work and motherhood. and when she returned to the workforce once her son was an adult, it reared its ugly head. it took about a decade to fully disable her. it took a toll not only on her body, but her brain. her initial admissions to care were in the locked ward.
i walk w my dearest of friends, roberta miles, because she too lives in the shadow of this beast. but she does it with a style and grace that mostly able bodied me can only dream of. she sings, she tells stories, she makes art, she teaches, she produces several long running shows, including loose chicks monologue group. i had the pleasure of making my debut as a storyteller w the chicks at my urban farm, moahs ark.
fortunately, roberta has had access to treatments that did not exist when my sister could have benefited from them. but she still struggles.
i want a world free of ms for her, and for every one who has to face this cruel killer.
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so, i've never made any kind of beg here for myself. this isn't rly 1 either, but it is. updated. (Original Post)
mopinko
Apr 18
OP
hunter
(38,325 posts)1. Kick for good walking.
mopinko
(70,202 posts)2. i'm so happy to b fit enough to do it again.
Niagara
(7,650 posts)3. Kicking for support!
mopinko
(70,202 posts)5. kicking this thread til i hear the jingle.
cmon, yall.
Loryn
(945 posts)6. Thanks for bringing attention to MS
It is truly horrible.
mopinko
(70,202 posts)7. the cruelest of all diseases, imho.
my niece, pattys daughter, also has it. she had a promising career in politics that fell apart when she started getting sick. it affected her behavior 1st. ppl said she had sharp elbows. she served 1 term on a county board. lost her re-elect.
My husband had MS. It is eating him alive. We preservere. Its hard.
Thank you for this
mopinko
(70,202 posts)9. if u pm me,
ill add him to my tshirt.