hello...becca here...this is to let you all know that my mil susan died on sunday. the funeral was yesterday. she has als along with dementia. she developed a bowel obstruction that landed her in the hospital...and because she was end stage als, they did not recommend surgery for the bowel...
i will say this one thing...
we have a similar situation...and at this point...when they are on a trache, and not able to eat or drink...it cant be long. once you see signs of end of life...(general) you know it will be short...hours...
hang in there...we're trying to too...
sincerely,
becca
hello there everyone,
becca here...i hope you are all coping with your situations as well as can be expected...
i have a question and would appreciate some answers if you have some...
my mil has als, and for awhile now has had a terrible cough reflex....now, her voice get so quiet as soon as she...
so sorry to hear
hello there...i am so sorry to hear about the diagnosed of your wife. als is a terrible disease...
i especially took note of your comment about being a terrible caregiver because of your feelings.....i am sure you are not terrible at all....
arent you just taking care of...
as far as i know
hello there...i am so sorry to hear about your loved one...although its true that noone can say for sure because each person is different...i thought that in order to receive hospice, the end had to be within 6 months time...so sorry to hear about all of this...it is a...
what i have heard
hello there...becca here...i have wondered the same thing and did get an answer to the question...once they need bipap close to 24 hours a day, thats when they switch to a vent...if they don't want that...well then, that would be it. as to how long it takes to get there...
answer to question
hello mary,
becca here...we wondered that same thing...when do they switch to the vent? finally we got the answer....it is when they need bipap 24 hours a day...then they go to a vent. at least thats what we were told, maybe someone else on this forum has additional...
hello.
hello there...becca here...i just read your post and only have a minute to reply...as for the bipap...i have found that most people w/als who have a fvc 60 or lower go on bipap...my mil's is 50. some docs start it even sooner as they feel the patient will be more comfortable longer...
good morning..
becca here...i was glad to see your post...i am so sorry about your mom..... it does cause a flood of questions and a lot of unknowns...
i will answer anything i can...as to the rilutek, yes we tried that, but it gave her serious uncontrollable diarea and that would not do...it...
good morning topsfan
good morning topsfan,
becca here..i just read your post and wanted to write and tell u how sorry i am to hear about your mom. my mil was diagnosed almost 2 years ago. hers began w/leg problems and was misdiagnosed for over a year. she is now in an electric wheelchair and...
how's your dad doing?
hi debbie,
becca here...just wondered how your dad is doing...? my mil is still declining...very much in the area of her dementia...now she has lost her legs, most of her arm strength...she has lost muscle in her hands...and her cough is very weak and has no force behind...
my mil
my mil has als w/dementia...what are you wondering about?
i will let you know what i can...anything to help.
so sorry for your situation
sincerely,
becca
answers i hope
hello there...my name is becca..my mil has als and was diagnosed a year and a half ago.
she has the als that causes dementia along with it.
she has lost the use of her legs completely, arms almost all the way and the muscles in her upper body are fading. her voice is much...
hello out there...becca here...could any of you let me know what progression you or your loved on experienced when bulbar symptoms set in and how long did it take to decline? my mil is at that point we thik...i would truely appreciate your input so maybe we can know what to look ofr.
thank u.
becca