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  • MS and brain fog: How do you cope with feeling ‘not quite like yourself’?
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Living with Multiple Sclerosis

MS and brain fog: How do you cope with feeling ‘not quite like yourself’?

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avatar Somya.P

Somya.P

Community manager
07/17/2025 at 10:00 PM

Good advisor

avatar Somya.P

Somya.P

Community manager

Last activity on 07/18/2025 at 4:52 PM

Joined in 2023


672 comments posted | 20 in the Living with Multiple Sclerosis group

23 of their responses were helpful to members


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Hi everyone, how are you holding up today?

For many living with multiple sclerosis, the focus often falls on physical symptoms like fatigue, mobility challenges, or pain. But there’s another side that isn’t always talked about as openly: when MS affects how your cognitive abilities work. 🧠

Some people call it “cog fog,” “MS brain,” or simply feeling slower, when words don’t come as quickly, names slip, logic feels fuzzy, or tasks that used to be simple suddenly feel overwhelming. It’s not about losing intelligence, but about feeling like the sharp, confident version of yourself isn’t always there anymore.

And it can feel isolating, especially when others don’t see those changes.

Have you experienced cognitive changes or brain fog with MS?

How do you cope emotionally with feeling ‘not quite like yourself’?

What helps you manage brain fog day to day, whether it’s humor, tools, or support from loved ones?

@Janell12965 @Nvrfazd @Cbean2017 @mickey @JamiKautzmann @Shiningstarspc @Keith6171 @Mjscruggs @EvaO2285 @jbenny86 @npolley @BWroke @SpiceC @lwallace34 @jbarrett @Rosemary8658 @Cgonlag @Neva1963 @Yaya62123 @Bunting5 @Amyisbomb @larsonlynn25 @Erniekel07 @Alisanna1 @Apegue30 @Bellabay12 @bwicher @Teresa406 @nonono @Jessinmike02 @Lreed6 @birdie64 @Pansy1950 @Raizyj @Vevans @caouterb @Mdestevens @Odie0713 @SPL30. @hmcalpine8 @Carter12 @Mtnhimama @Adamschiffer @AubreyTyler @Heathentodd @crock.99 @Jastanley9 @Ppetroline @Annafletes @jjdms5 @dan.varady @FBroo0713 @Lcrocs @PatriciaC @BobbiSchaef @Cheermom70 @lewisk1 @PattyLowery @Sissyyellow @Lejocos40 @Klundy2002 @Amysc76 @CHICKEN @katypugz @Mrsnurse @terrihill @Kat559 @sarjar @RobbieJ @KC-Walker @Odellpatty @Babster @Alesiavm07 @kinga3 @tonisnowt @Jrobles @Bbw4latinlover @jordanfolkes @veronicaevangelista @JaredW @JanessaA93 @RajaLP @Karyrodriguez7499 @Marimari628 @Irisms @msrozhou @Warc04 @KimberlyDana @Nholbr @Charley66 @Lolopez @LDRegert @peachia @pbwyatt @Suzhussey @Chiara31 @Christina @DeannaLynne @mlyons7961 @Steve67

This is a space where no one’s experience is too small or too “invisible” to matter, so feel free to share whatever feels right for you today.

Take care!

Somya from the Carenity team 🌼

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avatar dan.varady

dan.varady

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07/17/2025 at 11:00 PM

Good advisor

avatar dan.varady

dan.varady

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Last activity on 07/18/2025 at 5:17 PM

Joined in 2020


96 comments posted | 25 in the Living with Multiple Sclerosis group

6 of their responses were helpful to members


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I try to meditate and breath to bring me to a calmer state of mind.

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Dan Varady


MS and brain fog: How do you cope with feeling ‘not quite like yourself’? https://www.carenity.us/forum/other-discussions/living-with-multiple-sclerosis/ms-and-brain-fog-how-do-you-cope-with-feeling-not-quite-like-yourself-6323 2025-07-17 23:00:14

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