Injections are nefr easy to watch. A nurse at a rehab place told me this: If you're gettng an injection...& especially if blood is being drawn out, DRINK A LOT OF WATER JUST B4, & it will hurt less. Water pumps up the veins & liquifies blood more. : ) I have MG. MG is certainly NO picnic -- but it is the least serious of the neuro-muscular ailments, I'm grateful 4 that. (Lose weight, rest B4 ur tired,
keep positive attitude, when strong, excercise moderately.I've had MG a long time...)
Nice historic video! Who is/was this lady...& what did she lik 2 do? Wish she was dancing, & not doing floors, at 3:57! I hav MG & her eyes mov mor than mine, usually..efn at t beginning! But I'm stronger N al other ways. I tak a drug called MYTELASE...VERY expensiv, but works longer. Maks me feel almost normal...efn my eyes mov mor! But MYTELASE is N danger of being extinct. Ask OLDER drs. about it...if mor peopl tak it, mayb it wil continue.
I had the same symptoms all at once, and from the moment I was diagnosed and started on pyridostigmin and prenisone, it took me several weeks for my eyes to open, to eat, to stand and combe my hair by my self and as for walking... 2 years to walk normaly and even to stand up without help, son I don`t believe nor understand when people talk about the miracle of this drug, yes finaly the change came but the price you have to pay... but then again if it wasn`t for this drug it would be worse.
great! but we musn''t forget that is and advertisement from roche, that things aren't so easy en medicine, and exist adverse effects and contraindications.
Injections are nefr easy to watch. A nurse at a rehab place told me this: If you're gettng an injection...& especially if blood is being drawn out, DRINK A LOT OF WATER JUST B4, & it will hurt less. Water pumps up the veins & liquifies blood more. : ) I have MG. MG is certainly NO picnic -- but it is the least serious of the neuro-muscular ailments, I'm grateful 4 that. (Lose weight, rest B4 ur tired,
keep positive attitude, when strong, excercise moderately.I've had MG a long time...)
UTAOUB 1 year ago
Nice historic video! Who is/was this lady...& what did she lik 2 do? Wish she was dancing, & not doing floors, at 3:57! I hav MG & her eyes mov mor than mine, usually..efn at t beginning! But I'm stronger N al other ways. I tak a drug called MYTELASE...VERY expensiv, but works longer. Maks me feel almost normal...efn my eyes mov mor! But MYTELASE is N danger of being extinct. Ask OLDER drs. about it...if mor peopl tak it, mayb it wil continue.
UTAOUB 1 year ago
Apparently an English woman discovered the application of that medicine to MG.
azbobbieb 1 year ago
thanks to the man who discover that medicine!!!
acoh17 1 year ago
I had the same symptoms all at once, and from the moment I was diagnosed and started on pyridostigmin and prenisone, it took me several weeks for my eyes to open, to eat, to stand and combe my hair by my self and as for walking... 2 years to walk normaly and even to stand up without help, son I don`t believe nor understand when people talk about the miracle of this drug, yes finaly the change came but the price you have to pay... but then again if it wasn`t for this drug it would be worse.
ktyoruga1 2 years ago
great! but we musn''t forget that is and advertisement from roche, that things aren't so easy en medicine, and exist adverse effects and contraindications.
silbocacampeon 2 years ago
the eskimos would have left her on the trail...
s2who 3 years ago
That was great to watch.
aidanne07 3 years ago
classic
acoh17 3 years ago
Classic video. Pyridostigmine, Acetylcholinesterase. So many autoimmune diseases out there. Thymectomy.
dhukka123 4 years ago
i add to miastenia gravis.. and i got all that.. but now im so good... i only have the scar of my operation
constantinegirl 4 years ago
We can only hope she had a long pain free life in spite of her MG.
kleptodog 4 years ago