Research Update from The ALS Association’s National Office
December 9, 2008
ALS Association Co-Funds Study Showing Boosting the Body’s Detoxifying System Counteracts Nerve Cell Loss in ALS Mice; New Therapies Suggested
In a study that demonstrates a much-anticipated proof of principle...
als
als research
alsa
atrophy
battery
brain
cell
conversation
cure
death
enzymes
eye
familial
free
friend
grants
increase
information
lead
life
movement
muscle
muscles
natural
onset
power
published research
research
risk
robert
sod1
sporadic
stroke
support
switch
test
tests
therapy
update
work
young
I am starting to research information on grants to help pay for making a home handicap accessible. Our home has been on the market for over a year now. We have dropped the price twice, for a total of $20,000. Still hardly even any lookers. I have been scoping out what is available in our...
To All:
Please find below an email I sent to Coleen Maguire yesterday. The reply she sent me is very informative. For all you Okies, please let this senator know not to keep blocking the ALS National Register.
If any of you are interested in the links she refers to, email me off line at...
advocacy
age
als
als registry
alsa
back
cals
caregiver
cdc
cost
data
disability
early
family
grant
grants
helpful
home care
increase
information
insurance
money
nursing home
questions
respite
senate
support
va benefits
veterans
wanted
website
Hello all, I've been hanging around on and off for a bit. As you may or may not know, I got my diagnosed in May of this year. Since then I've been learning everything I can, trying to plan ahead and spending more time with the family but I am still working. Retirement is not an option at this...
I have a friend with ALS whose family is curious about any programs that help defray the cost of in-home care. I've spoken to ALSA, Medicare and a home health care agency, and no one is aware of any needs-blind programs. Anyone have any help? (The insurance covers medically prescribed visits...
Received this email today, and wanted to share:
--------------------------------------------------------------------------------
The Amyotrophic Lateral Sclerosis Association, Capital Office
601 Pennsylvania Avenue, NW, Suite 900, South Bldg., Washington, DC 20004
(202) 638-6997 * Toll-free...
Has anyone taken the 8 weeks caregiver leave through unemployment and does anyone else know of other grants or organization tHat help out financially.
my husband Has been diognoised for 6 1/2 years and i feel it is time for me to be with him. it was Hard to accept tHat i was going to take this...