Hi............Sorry. haven't been able to be here for awhile I spent 7 day's in hospital with heart failure then had to return to the hospital 3 time's after I was discharged...
Anyway's had my husband a apt @ U of U clinic but they called to confirm insurance and told me that our insurance was...
I just feel I need to get some of this toxic energy out of me and this is the right place to do it with the right audience. These are some of the thoughts I get on the worst of days.
1) My situation. Just before diagnosis I went through a relationship break-up. So I have no wife, no kids, and...
Apparently getting social security isnt a given for the spouse when the pals dies. It is age dependent. My son who has several disabilities, is being evaluated under the disability area as well as, the survivors benefits. We had been told previously he wouldnt qualify because of my earnings...
Hi all, I'm Katy As much as I love new groups, I really wish this is one I didn't have to become a member of. No offense to all you great people. After about a year or so of slurred speech and my voice being reduced to a hoarse whisper, my GP sending me to a neurologist and months of testing...
Respite care is one way to take care of ourselves as caregivers. It gives us a little relief so we can do things like visit with friends and family, go shopping, or go sit somewhere and do nothing if that is what we choose. It is not specific for caregivers of a PALS, but we can benefit, as well...
Good morning,
I am new to this group; and haven't spent a ton of time because the reading makes me want to hide!
I was diagnosed with bulbar onset ALS in June of 2015. At the time I was dealing with slurred speech and swallowing probkems. Now, 8 months later, I cannot speak, soft foods only...
Hi everyone,
I am newly diagnosed (12-29-15) with ALS. Since my dx, I've been devastated.
My mom passed away in August and I was in a pretty deep depression over that when I got my dx a couple month later. I feel like I was hit over the head with a sledgehammer, and that wasn't enough so I...
als
arm
breathing
dementia
depression
disability
dry mouth
emg
heart
lyme
lyme disease
memorial
mri
myasthenia gravis
neurologist
newly diagnosed
sad
second opinion
speech
story
support
swallowing
test
weakness
wrong
Caregivers of veterans with ALS are welcome to join a community of military/veteran caregivers.
The Elizabeth Dole Foundation was created to assist and support military/veteran caregivers. "Our nation’s military caregivers need and deserve robust, effective support in light of the mental...
Hello everyone. My name is Curtis. I am a 45 year old husband and father. I was diagnosed just before Christmas with ALS, though I had strongly suspected that I had it for a few months prior.
I am on active duty in the Navy and am now going through a medical board which will medically retire...
advice
als
christmas
cramping
diagnosed
diagnosis
diet
disability
family
father
hope
medical
muscle
problems
progression
speech
supplements
support
swallowing
Hello, I have been paying Cobra since I left my previous company and started at my new company. I needed to keep Steve insured and my insurance was very good with no deductibles.
His disability was finally approved today and he now has Medicare A and B. I am having a hard time figuring out...