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Living with multiple sclerosis

Going downhill fast from PPMS

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avatar Christina1958

Christina1958

13/06/2025 at 05:03

avatar Christina1958

Christina1958

Last activity on 10/02/2026 at 02:04

Joined in 2015


6 comments posted | 4 in the Living with multiple sclerosis group

1 of their responses was helpful to members


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Anyone else rapidly declining with PPMS? When is it decided you have progressed to the next stage? How bad do you have to be?

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avatar Somya.P

Somya.P

13/06/2025 at 18:09

Good advisor

avatar Somya.P

Somya.P

Last activity on 13/09/2026 at 02:43

Joined in 2023


1,115 comments posted | 39 in the Living with multiple sclerosis group

110 of their responses were helpful to members


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Hi @Christina1958,

Thank you for sharing something so difficult. I’m really sorry to hear that you’re experiencing such a fast decline, it must be incredibly difficult and overwhelming. Primary progressive MS can bring a lot of anxiety, especially when it feels like your body is changing faster than your doctors can respond.

Unfortunately, with PPMS, progression doesn’t always follow clear stages like in other conditions. It often comes down to noticeable changes in mobility, daily functioning, or new symptoms that don’t improve over time. But you shouldn't have to wait for things to get “bad enough” to be taken seriously. If you haven’t already, it may help to keep a symptom diary and bring it to your next appointment. Documenting even the smallest changes might make it easier to push for proper care.

To others living with PPMS:

🗨️ Have you experienced a sudden or rapid decline?

💬 When did you decide to talk to your doctor about progression, and what helped you through?

@csgamble @shellmo4 @monkeymaggie @Fluffy @Steve62 @Tommotoo @Georgie @casper34 @Rolley @Hoofah1 @greecetogo @fran42 @bethen @Bitch270 @Pyjamaqueen @sueseedy @ragerty @pavo123 @bambi13 @1eyedjack @jaynedebra @Zlg2070 @Ladyisis71 @Gemzied @Lynn49 @kathy52 @SuSaBa @Loobysedg74 @giggi61 @tmpk28152 @DonnaBR @Charliecat @Nikkim @carless1 @Kencomax @melissawall @Karanja2012 @adreeves @MargaretP @FredaBurke @Mazb1982 @Yvette53 @Claire65 @AliSyn @blackshades @bigk @Ozzie5120 @Sandy1958 @Gay140 @Pricey @Mandymca @Sallyvalentine @Jules13 @CarmenRajput @Alvina @Shelah @Jeanweeks @Thissyanne @KayWlk @Daisybuster @Tracey1971 @Juliemoore11 @Monicaspencer13 @Zoey51 @BadgerCowell @Mollie07 @Chalmm @Lisahodgkins @Sk8rGirl @Doitforkyle @2212dianne0 @Salsybar46 @Charlie219 @Sonialb @LindaBlacker @FitzyDebs @vonnywonkie @Jemgavlaa @Oliviac09 @Iamsue @Michelle166 @Bernieleonard @Lorraineredmond @StevieC @Batchelm @Elbie1 @Mattyh75 @Deedeenone @Jax1980 @Yvonne3101 @Faye1512 @EmmaMilo @Gohare @Trainor84 @Rose1962 @murraygrant @volvof88 @ColinSalter @alexab @revdonahue

You’re not alone in this. Your experience deserves to be heard, and I hope you’ll keep reaching out.

Take care,

Somya from the Carenity team 🌼

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Somya from the Carenity team 🌼


Going downhill fast from PPMS https://www.carenity.co.uk/forum/other-discussions/living-with-multiple-sclerosis/going-downhill-fast-from-ppms-5736 2025-06-13 18:09:48

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