Surviving my MS life survey...just saying!...Because I am kind of limited as to 'ability' these days, I ask HIM to use my words that I write so that they might comfort or entertain or... By shep04546 min readBookmark for laterReactions 0 reactions Comments1 comments
PPMS: Cognitive Decline Does NOT Have Me!!!...Although not necessary for functional living, the ability to perform IADLs can significantly improve the quality of life.... By folaketaylormd7 min readBookmark for laterReactions 0 reactions Comments5 comments
How to deal with a rapidly progressing disease...., UTI’s and recently Covid take all strength and mobility away both sending me to the hospital to recover....Reactions 0 reactions Comments1 repliesCaregivingPPMSCoping
Michelle's MS Story...I lost my ability to speak like a normal person. I was stuck stutterring and searching for words. I could not talk hardly at all.... By taxigirl20038 min readBookmark for laterReactions 0 reactions Comments4 comments
MS Kicking My Butt, And I'm Kicking Back......But slowly losing the ability to walk and not knowing why, that was the not so good news, I guess.... By rolly18 min readBookmark for laterReactions 0 reactions Comments8 comments
Are your adult children involved?...until they were in their early 20s that my wife descended from remitting relapsing MS into the secondary progressive stage of MS, and lost most of her ability...Reactions 0 reactions Comments1 repliesCaregiving
Late-life onset - some of your symptoms may be age, not MS...And, of coure, memory problems...menopause did a number on my recall ability....Reactions 0 reactions Comments1 repliesSymptoms
A Fine Line Between MS and Depression...The ability of doing simple task is draining. Going anywhere or doing anything becomes crippling.... By ms-slayers11 min readBookmark for laterReactions 0 reactions Comments5 comments
MS & Comorbidities! How do your other medical issues combined with your MS impact you?...I’ve also experimented with multiple adaptive devices over the years to make some tasks a little easier. That said, it’s still a huge issue for me....Reactions 0 reactions Comments81 repliesAwarenessCopingSymptoms
Does anyone know what CMS/HCC stands for?...I've been on Aubagio for 10 months now and started having new symptoms, constant pain in my spine, on and off dizziness, and losing the ability to retain...Reactions 0 reactions Comments3 replies
Suggestions for dealing with sensory overload?...The slightest sound can throw me over the edge, and my ability to focus on more than one thing at a time has become impossible....Reactions 0 reactions Comments4 replies
core temp...So now I need to figure out how to continuously monitor core temp, I'm looking at a device from corebodytemp.com . any thoughts?...Reactions 0 reactions Comments4 repliesTips & AdviceFatigueExercise
Zeposia...My neuro said he's not worried about my physical ability (as MS as not effected it yet) but he's concerned with my brain and the atrophy that has taken...Reactions 0 reactions Comments1 repliesTreatment
Bandaid Solutions...The device that I formerly used to help my wife transfer from the wheelchair into and out of the passenger seat of the car no longer works so that...Reactions 0 reactions Comments2 repliesCaregiving
Trying to work...I’m doubting my ability to work even part time....Reactions 0 reactions Comments1 repliesCoping
My MS Story...We've heard that a lot over the last year when it comes to things like gender and race, but it's just as prevalent with MS or any other differing By campbellgn13 min readBookmark for laterReactions 0 reactions Comments2 comments
Would you like this?...An MS diagnosis is not the entrance to immobility and slow deterioration....Reactions 0 reactions Comments5 repliesCaregivingDiet & NutritionExercise
What are some things you are proud of accomplishing despite MS?...My cognitive issues have really impacted my reading ability in recent years (I've written about that here if you are interested: https://multiplesclerosis.net...Reactions 0 reactions Comments7 repliesSymptomsCoping
Has anyone else lost the ability to automatically not speak everything you are thinking?...For the past 3 years or so I have started to speak everything I am thinking without wanting to. I can think in my head but only when I am...Reactions 0 reactions Comments4 repliesSymptoms
I would like some thoughts and feedback from people with progressive MS...We watched her decline rapidly in a period of two weeks - she lost her ability to eat and drink and speak, had what was probably a seizure or...Reactions 0 reactions Comments3 replies
