I AM ASKING PROGRESSIVE M.S.ers AND ALS- MND PATIENTS IF THEY WOULD RATHER STAY HOME OR BE IN A NURSING HOME. I AM ASKING WIFE OR HUSBAND OF A PROGRESSIVE M.S.ers AND ALS-MND PATIENTS IF YOU WOULD LIKE YOUR SICK SPOUCE AT HOME OR PUT IN A NURSING HOME? WHAT HAPPENS TO ALS-MND PATIENTS WHO NEED TO BE ON A FEEDING TUBE-BAG AND VENTILATOR? IS IT TRUE THAT VENTILATOR PATIENTS MUST LIVE IN A HOSPITAL? THEIR ARE ONLY 20 ALS-MND NURSING HOME BEDS. margaret.cabral22@gmail.com
Trying to keep independence is the best thing we can do. I have Prog. MS for almost 30 years. Every week I feel some ability just disappear, is hard but....my wife's my caretaker.
thank you bjorn, too bad your book is written in swedish i can not comprehend. i have progressive multiple sclerosis, wishing you all the best you deserve. a hug,
Please Sign My Petition To Support The Stem Cell Research Enhancement Act that could help my Brother (and thousands more) With ALS-Lou Gehrigs Disease. There are no Cures for these and many more horrible death sentence of Diseases.
Please Help! Go to i p e t i t i o n s .c o m and searach for als.
The391956 1 year ago
Nice video, just wish the sound was better quality
latensune 3 years ago 6
I've Progressive MS (not sure if it turns MND) nice to see you arrangements in order to keep your wife away from a nursing home.
Peace and Health,
Sefardisafran
Hoboken NJ
USA
Sefardisafran 4 years ago 2
Trying to keep independence is the best thing we can do. I have Prog. MS for almost 30 years. Every week I feel some ability just disappear, is hard but....my wife's my caretaker.
Hugs,
Sefardisafrán
Hoboken NJ
USA
Sefardisafran 4 years ago
thank you bjorn, too bad your book is written in swedish i can not comprehend. i have progressive multiple sclerosis, wishing you all the best you deserve. a hug,
luism
hoboken nj usa
Sefardisafran 4 years ago
Alex my wife is my carer, she is my only boss.
luck and much hugs
luism
hoboken nj usa
Sefardisafran 4 years ago
Please Sign My Petition To Support The Stem Cell Research Enhancement Act that could help my Brother (and thousands more) With ALS-Lou Gehrigs Disease. There are no Cures for these and many more horrible death sentence of Diseases.
Please Help! Go to i p e t i t i o n s .c o m and searach for als.
ALS-Advocate
fightingforals 4 years ago