Sorry I haven't posted much lately. However I have been reading every morning since most of my days start at 4am.
I had a visit from my OT and Nurse, lovely ladies. First off they wanted to know if they were getting too pushy by coordinating equipment. They want to have lifts, etc...in place...
anger
caregiver
chair
cry
depression
equipment
eye
family
frustrated
hospice
kids
lifts
pain
power
power chair
problem
reading
stages
swallow
transfer board
wanted
wheelchair
work
Reader beware - this is blunt. My husband was diagnosed with bulbar onset ALS in May 08. He started slurring his speech in Mar 07 and, after ruling out stroke, doctors figured it was the progression of his Multiple Sclerosis (which he was diagnosed with in 2000). Yes, both M.S. and A.L.S...
als
anger
botox
bulbar
bulbar onset
caregiver
chair
choke
choking
death
diagnosed
family
fear
food
friend
ftd
guilt
hope
ideas
insurance
life
medical
night
onset
peg
problem
progression
shower
speech
speech device
stroke
surgery
voice
My Mum died on New Years Eve and was such a star in battling this disease. It was so rapid for her after Dx in August.
The thing is that the funeral is soon and awful sibling is pulling strings - I just want to go with the flow but am being completly blanked . How do I get through this day ? Am...
Just thought I would chime in and proclaim my presence. I started having problems with my legs 7 0r 8 years ago. I mentioned it to my Gyno and he sent me to the Rheumy who sent me to a Neuro. The first Neuro told me it was depression. :roll: I knew better. The second Neuro did the tests and...
My Husband was told that he has ALS and had 5 years to live. Later it was discovered that he has the toxin trichothecene. After 5 rounds of plasmapheresis he was ABLE TO STAND UP AND TAKE A FEW STEPS. But(for some reason I cannot fathom) the doctors said that was NOT AN IMPROVEMENT but a "fluke...
als
anger
bed
call for help
clinic
food
free
grief
improvement
life
music
pain
paralysis
power
power wheelchair
scooter
treatments
trichothecene
wheelchair
work
I am having a difficult time dealing with my anger. My DH was DX 8/07. With the exception of his sister who lives in another state, we have had absolutely no family support whatsoever. Both his adult son and his brother live an hour away. I have asked for their help in a very clear manner. The...
Hi, all ....
I know about 20% of PALS also have FTD (frontotemporal dementia), and I think I am one of them. The speech pathologist at UCLA agrees with me (or rather, I agree with her that I have it), and I have some appointments coming up to look at this.
My problems started this spring with...
Hi. My name is Erin and I am new to this site, so I hope there are some caregivers out there that can relate. Thank you to those that replied to my first posting. My husband was diagnosed with ALS May of 2007 at age 35. We had a baby girl the following October and in February we moved long...
We're having a terrible time getting my husband set up with BiPAP. First of all, on May 21st at our initial visit to our local ALS clinic the respiratory therapist (RT) told us which company she was selecting assuring us that the BiPAP machine would be delivered and set up the following week...
Hello all!
The past few weeks have been incredibly hard, and as a result my mother suggested that I seek support from others who understand this terrible disease. My father was diagnosed in October of 2005. He had just turned 50 and began getting arthritis symptoms in his hands. In January 2006...
ability
anger
back
bed
bed sores
boyfriend
decline
depression
diagnosed
diagnosis
eyes
family
father
feeding
feeding tube
grief
healing
heart
hospice
movement
story
support
symptoms