my wife had PPMS for about 20 years and the last 10 years she is end stages MS. ESMS isn't something usually discussed here or anywhere for that matter.
ESMS is when you have lost everything. cannot walk, talk or eat orally anymore and fed via Nasal Gastric Tube or peg system and technically 100% bed ridden.
My wife certainly went through what everyone is saying here, depression suicide etc....
So after about 11 years of ESMS she still smiles every day and i take her out every day driving site seeing.
We don't mix publicly with people as its a health risk so we are solo all the time and make our own fun.
Its much harder for those without the 24/7 support thats needed.
ESMS is when you have lost everything. cannot walk, talk or eat orally anymore and fed via Nasal Gastric Tube or peg system and technically 100% bed ridden.
My wife certainly went through what everyone is saying here, depression suicide etc....
So after about 11 years of ESMS she still smiles every day and i take her out every day driving site seeing.
We don't mix publicly with people as its a health risk so we are solo all the time and make our own fun.
Its much harder for those without the 24/7 support thats needed.
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