My brother moved in with me in 2015, I have read up on neurological food and I believe feeding him these helps.
Horrible disease, more money needed for labs to research this and find a cure.
Praying alot!!
Multiple System Atrophy diagnosed 1 year ago
Multiple System Atrophy diagnosed 1 year ago
Newly diagnosed MSA Patients connect with me.
Dietary restrictions: No gluten, no soy, no alcohol
Physiotherapy
My new great granddaughter Madison
Academia todos os dias
Please join or start a local support group to meet others.
My heated blanket and my heated throw in the recliner.
botox for neck pain
clonazepa at night and Zoloft also Macrodanian
Humour, in any way or form.
The use of gabapentin for pain of my nerves
supportive family and doctors
I have a wife who helps me do all my activities and is my 24/7 caregiver.
Local health professionals/ internet/ support group
Comfort
Coq10. 3000mg
My faith and optimistic outlook
Great Doctors and therapists/
Having friends and family who love and support me
Planning for Future
Insisting the doctor let me try carbidopa/Levodopa, it works in 40 percent of MSA cases. It has helped make a difference with my balance and coordination. Also, my endocrinologist prescribed "Omnitrope" the human growth hormone, (hgh) helping me to keep m
steriods
I have a very tight knit group of doctors coordinated by one internal medicine specialist.
Electric wheelchair
Excellent physician care in Florida and Boston
Though not a carer anymore I'm still happy to support those who need direction.
Walking with crutches since a year, have a feeding tube in my stomach
My lovely caring family, support groups & friends....some with MSA or PD & some in good health......
Moving muscles, as much exercise as can tolerate to keep movement for as long as possible
Being given loving support of many kinds by family and friends.
http://kathyjwhitemsa.webs.com Blog. Products that help manage.
he sue of a recliner improved my nOH
My wife's support she doesn't complain at all
my husband, always asks my opinion on things.
My wife's support.
ter um remédio nas eficaz
Stay employed
Therapy
Great husband and family and medical community
Take the time you are given to relive memories and make new ones. Laugh. Do as much as you can before the next stage of the disease takes hold.
Disability insurance allowed for Dad to stay at home with paid caregivers.
That potentially disease-modifying drugs undergoing trials for Parkinson's might be re-purposed for MSA
cilift keeps me from being depressed
The Assisted Living facilities my Dad has lived at.