MS Fatigue

At least someone is not pushing meds down the throat of the patients. Kudos to that 👏🏻

I experience fatigue.

Being diagonosed very recently, i cry alot more know :), :(, not the worst thing that can heppen but knowing your braind is malfuntionning...ye alright...

I feel your pain, stage 4 osteoarthritis, degenerative disk and joint disease, and PPMS.

I think this may sound crazy but can you have a great deal of the symptoms of MS but even tho you go thru most of the tests for diagnosis still the doctors tell you you don't have it?

Ill never feel ashamed for being disabled, you shouldn’t either. God Bless

100% experiencing this with a incline

I walked in AZ for Team Trevis! Hugs

How exactly are you treating your MS, Tinnitus and COPD? I got mine treated and cured with a herbal medicine from Dr Madida.

I couldn't walk a week ago... I faught my way back with the help of my Neurologist Nurse Practitioner (She's amazing)... Did my full PT and walked today... Trashed...

Got my MS in my early 40s but it was in remission for about 20 years and not diagnosed until my early 60s. I worked part time while raising three kids and my symptoms were rather mild until my mid to late 60s. My fatique is more depression related and having to get up at night to use the loo so I often have to catch up on the sleep I lost though I'm sleeping better now after 20 years of insomnia. Many top psychologists worldwide and people with MS in the UK where it's very prevalent esp. Scotland have linked MS to trauma, how about caused by ongoing stress since childhood and many experts have linked it to psychological trauma and great loss! How about we start linking MS to not only the physical body but to the mind and spirit as well, the body, mind and spirit connection since it's all connected i.e. HOLISTIC health! Many top psychologists have linked MS to emotional stress and state that too much chronic stress has created auto-immune diseases, not only MS and leading researchers in the UK have said it goes all the way back to the Vikings! I'm of English/Scottish/Irish background on my maternal side with a little French. There's a very high rate of MS in Canada, the UK and in Aberdeen Scotland where my ancestors were from, but there is no record of anyone in my family history with MS. Also, very high rates in the Orkney/Shetland islands just north of Scotland and anywhere above the 37th parallel due to lack of sunlight, hence the need for Vitamin D3 with K2 which helps the body to absorb the D3. "knowledge is power"....self-empowerment!

did not learn anything new..as a patient i know if i dont sleep enough fatigue will be more, if i am stressed, there u go, muscle tension, even if you walk more it comes or my fatigue will be at constant mode...i cannot afford to yell at my kids nor can i have an argument with my husband. if i maintain some easy in my system, i can manage my chores..if some body starts an argument with me, thats mono acting for them..

With a neurological condition outside the usual spectrum is very much more important without the military structure forcing me into doing physical activity in spite of difficulty or neurological conditions

The importance of good Sleep hygiene is something I needed to be mindful of during my active duty career, for best survival and overall health/well being.

Traumatic brain injury has given me a fatigue burden I had not experienced while I was an active duty army soldier for three years. 13 years of living with a traumatic brain injury has given me a very esoteric perspective of life I'm needing to do something with to benefit myself and everyone else involved.

I will be willing to give

Then work ups

Then general analysis

Patterns of beating defamationort Paton I think

Heavy legs 🦵

I wish people could & would understand

This guy admits chronic fatigue is usually the first symptom . so it's happening months or years before people are even diagnosed , on medications or even before they have a chance to be depressed about a life changing illness . He makes zero sense . I wouldn't wish ms on anyone but I wouldn't shed a tear if he was diagnosed and had to learn the hard way he's wrong .

I’m 16, and I’m like “yeah, Exercise is good for cognitive problems” while laying on my bed.

Not the same as thyroid tiredness, aneamia weakness lol. I have all of these. You ra not really a specialist until you have it. Then things would become clearer.

fatigue from depression IS NOT the same.

I suspect I may have ms. I have celiac, undiagnosed for 45 years. Often times I will say I feel as if my blood was drained out & replaced with liquid lead. All day on the couch on those days but I hate sitting for too long because the longer I sit the harder it is to get up 😢

My guess is depression is a symptom but not a cause of fatigue. Hard to not be depressed if you're exhausted.

I know exactly how the guy who describes lay down or fall down feels. MS fatigue is so debilitating I hate it

New to me is Turning heater on 67 and it makes me have vertigo and fatigue is up 90%

I was wondering if vitamin D The fishency causes Fatigue because I was diagnosed with this and put on 5500IU1per week and then this new doctor went and checked my vitamin D level and told me to cut down on my vitamin D intake and I did but now I seem to have worse fatigue and I don't know if my Vitamin D is causing this problem

No one knows so don’t say it’s depression

Depression and mental illness talk is such a scapegoat

With ms fatigue I feel like I’m encased in concrete trying to walk in wet sand

Kudos for the Video! Forgive me for butting in, I am interested in your opinion. Have you ever tried - Seyrooklyn Salient Supremacy (google it)? It is an awesome exclusive product for overcoming the symptoms of multiple sclerosis minus the normal expense. Ive heard some incredible things about it and my work colleague after many years got astronomical results with it.

Cheers for the Video clip! Forgive me for the intrusion, I am interested in your initial thoughts. Have you heard about - Seyrooklyn Salient Supremacy (do a search on google)? It is an awesome one off guide for overcoming the symptoms of multiple sclerosis without the hard work. Ive heard some pretty good things about it and my old buddy Taylor at last got cool success with it.

This video is the best description of MS fatigue I have heard yet.

Highest MS rates are in Washington and Vermont I read. Here in WA we usually have low Vit D levels from lack of sun. Which I found thru blood test 2years B4 MS diagnosis

Went back to work recently doing two hour shift for some money. I use to do twelve hour shifts without a break in a kitchen and not be remotely close to how tired i am after just two. I go to work for two hours then end up in bed all day! People really don't know what i mean when i say i'm tired, i get so tired it takes effort just to respond to people.

What about ME/CFS?

Kudos for the Video clip! Excuse me for chiming in, I am interested in your opinion. Have you considered - Dinanlinson Rebooting Health Approach (google it)? It is a good one of a kind guide for getting rid of chronic fatigue syndrome minus the hard work. Ive heard some pretty good things about it and my old buddy Taylor got astronomical success with it.

I would literally give away a limb to not feel this way all the time

This discussion is BS. The usual BS from individuals looking to maintain a career, rather than help others.

My biggest issue is the cognitive impairment resulting from fatigue. It's truly debilitating.

But one thing is for sure. I cant be arsed listening to specialists discuss symptoms. I want to gear solutions.

My experience is it isnt fatigue. It's a complete shutdown of my system in order to preserve brain function.

I have to down "tools" and allow my body to "reset".

I can turn to glucose when I feel an attack coming on.

Lassitude exactly expresses my fatigue. I’m always needing a nap. I am not depressed, though have been in the past, and had CFIDS in the ‘90s. This is different.