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Registered Company: 06000961

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Sort 1059 results by
Recent activityNewest posts

@Dnorwood 

Dnorwood

PPMS

I’m just wondering if anyone with PPMS has anything that they’ve tried. This is a new experience for me so I’m open to suggestions that’ll help.
First posted on the Shift.ms app

@Joannelouise 

Last reply

Joannelouise

Ppms

So my neurologist thinks I have PPMS. Should I be worried?
5

@Lester 

Last reply

Lester

Ppms

I've been diagnosed with primary progressive MS I'm 45 was very active. I know it's a question everyone will ask. I have a young family and need to try and support them by continuing to work. Is it likely I'll work until I retire. Am I likely to walk without crutches?I can't walk very far anymore. R...
Birmingham, United Kingdom
  • Work and play
  • Exercise
  • Healthy living
  • Diagnosis
  • Newly diagnosed
  • Family and children
  • Primary progressive
  • Work and Study
15

@loulou 

Last reply

loulou

PPMS

Hello all I apparently have PPMS I often feel alone reading posts and chat as most people talk about RRMS, feel quite alone sometimes, say hello if you have PPMS so we can talk about OUR MS and compare notes!
  • Primary progressive
  • Diagnosis
  • Relapsing remitting
21

@watsoncraig 

Last reply

watsoncraig

PPMS

Primary progressive multiple sclerosis (PPMS) is one of the rarest of the four forms of multiple sclerosis (MS), making up approximately 10 percent to 20 percent of MS cases worldwide. Like other forms of multiple sclerosis, PPMS is an autoimmune disorder that affects the brain, spinal cord, and opt...
Falkirk,GB
  • Balance
  • Diagnosis
  • Primary progressive
  • Secondary progressive
  • Symptoms
  • Fatigue
  • Numbness
  • Work and play
  • MRI
  • Mental health
First posted on the Shift.ms app
8

@PeterW 

Last reply

PeterW

PPMS

I am new to this site and wondered how many people with PPMS used it? Really interested to hear other people's experience of PPMS. I was diagnosed three year ago after investigations into what was then a mild gait/drop foot problem. Over the past 18 months I have experienced significantly greater...
  • Pain
  • Symptoms
  • Diagnosis
  • Primary progressive
  • Healthy living
  • Exercise
  • Balance
  • Newly diagnosed
  • Treatment
  • Work and play
25

@Mithria 

Last reply

Mithria

PpMS

Two weeks ago I've been diagnosed with PPMS, I was chosen for FenTrepid program what has scary side effects, I don't know would it help me😔 I'm not living now normal life.. Is there anyone with this diagnosis and using this treatment maybe?
  • Diagnosis
  • Primary progressive
  • Newly diagnosed
  • Treatment
8

@Mavrikis 

Last reply

Mavrikis

PPMS

Hello group, this is my first post. I was diagnosed with PPMS here in Greece almost 3 years. I just had my 4th Ocrevus dose. My walking is not that great and I’m tired a lot. Would love to hear advice from you. Thanks
  • Diagnosis
  • Newly diagnosed
  • Healthy living
  • Ocrevus
  • Exercise
  • Primary progressive
  • Treatment
  • Symptoms
  • Fatigue
29

@Joparrott1978 

Last reply

Joparrott1978

PPms

Hi all hope all well, I finally got my diagnosis yesterday after seeing my neurologist, I have ppms which I wasn’t expecting, but feeling ok about it , it is what it is, why is there no treatment for this ms, or is there I don’t understand really, will my ms nurse explain this to me, my neurologist...
  • Diagnosis
  • Primary progressive
  • Treatment
  • MRI
  • Symptoms
42

@markms 

Last reply

markms

PPMS

HI all ppms come on in to the ppms group say hi its getting to quiet in the group lol
  • Primary progressive
  • Diagnosis
  • Disclosure
  • Ocrevus
8
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