#relapsing-remitting

7 Aug 2018 08:26Last reply 7 Jan 2019 13:06

MS buddy

Hi all Hope you all are having a day. I’m Gemma (34) I began have sympsons in spring 2013 but the doctor never seemed to put them all together so my offical diagnois of relapsing/remitting didn’t come till 2016. Im December 2017 a MS consultant said I was that the diseases had progressed to second...

17

@chloeautumnx

24 Apr 2015 08:26Last reply 25 Apr 2015 14:11

RESRRMS

Hi there! I wonder if any one could share their experiences on this. I recently went to my neurology appointment where we discussed medication, I was assessed and we looked at my previous MRI results. I saw a different neurologist this time and she interpreted the MRI scan again. She stated that ...

16

@Gemma1988

10 Aug 2014 07:10Last reply 17 Aug 2014 15:51

New to ms

Hi, just wanted to post say hello... I was diagnosed in May 2014 with relapsing remitting ms... It's been quite a journey I'm 26 and a mum to 2 little girls age 4 and 2 and getting married in November. I've been so scared of the diagnosis and suffering a lot with anxiety! Hoping to hear some good st...

16

@Julesds1977

15 Jul 2018 15:08Last reply 23 Jul 2018 00:17

Recently diagnosed!

Hi everyone, I have just been diagnosed 3 weeks ago with relapsing remitting MS. I have been experiencing problems with my balance, skin numbness and tingling in my legs since December 2017 when I was signed off work. I'm currently still off work now as I've still got residual symptoms from what I...

16

@Lynette09

27 Jun 2017 18:30Last reply 29 Jun 2017 19:22

Lemtrada

Hi Everyone I was diagnosed a couple of months ago with relapsing remitting ms. All tests complete, lumbar puncture, another brain and spine MRI so now focus is on DMD's. Appointment with my ms nurse last week was going through the different treatments my neurologist had suggested. I was between Tec...

15

@mscole

23 May 2017 05:59Last reply 23 May 2017 18:15

How Do You Handle Stress? I HANDLE IT!!!

Hello, everyone! My name is Nicole and I am new to Shift. MS. This is my first post. I was diagnosed with Relapsing-Remitting MS in December of 2015. For me, it was a quick diagnosis. One July evening I went to bed and awoke the next morning with my left hand numb. I, of course, went through the ty...

15

@Andrew_Tarpey

6 Jan 2016 19:23Last reply 15 Jan 2016 12:22

Choosing a treatment

Hey I'm new here after being diagnosed in mid-December with relapsing remitting MS. The two neurologists I've seen have both been keen to get me started on treatment. I am currently in my 3rd year at university though, and am worried about the side effects medication could have on my ability to do ...

15

@Peacezone

5 Apr 2018 19:42Last reply 8 Apr 2018 13:12

Recent diagnosis

Hi, I'm very recently diagnosed, last month in fact. I'm 36 mum of three and soon divorced, so all of this had happened very quickly and is Very overwhelming. At the moment I have hardly any symptoms apart from numbness but I'm really scared of getting some of the symptoms and whether they will remi...

15

@166wow

25 Aug 2017 12:43Last reply 28 Aug 2017 15:50

getting up in the morning

Do other MSers find getting showered and dressed in the morning exhausting? I have to lie down again the recover!!! I have had relapsing remitting MS for almost 25 years.

13

@evieb

26 Jul 2019 16:11Last reply 27 Jul 2019 09:11

Mavie & Me

I have RRMS (relapsing remitting ms) I am quite a private person who has never before posted anything on Facebook. I cook badly so wouldn’t get many, if any likes and my children are both late teens so there aren’t any best in class forward roll or cycling proficiency certificates to show off and as...

13

@Almost

10 Oct 2016 13:37Last reply 12 Oct 2016 11:11

Just Been Bullied By Neurologist

So, after, what turned out to be a relapse about a year ago, I was diagnosed this January with relapsing remitting MS, after two MRI's. I decided against having any treatment, as I wanted (and still do) to try and control the disease with diet, nutrition etc and see how it went. So far so good, I fe...

13

@Tabbycat

13 Dec 2014 21:32Last reply 17 Dec 2014 21:14

RR to progressive ?

I am due to see my neuro soon . I have been diagnosed as relapsing remitting, but have not had a relapse for two years. During that time lots have things ( walking distance, balance, spassicity of muscles etc) have got slowly, but noticeably worse. I think I have had Ms for at least 12 years and am...

13

@sigmadelta

31 May 2017 20:45Last reply 4 Jun 2017 20:49

It's a Ghost in the Machine

I've had MS for 26 yrs. It's gone from almost un-noticeable to relapsing remitting to secondary progressive in the last 2 years. In spite of countless scans, examinations and consultations... one thing has become quite clear. NO-ONE has any idea what they are dealing with. Treatments are for symptom...

12

@Kimberley11

16 Feb 2017 13:22Last reply 22 Mar 2017 17:25

Is Personal training helpful for MS?

Hi, I have had relapsing remitting Ms for 3 years now and I'm doing relatively well. I'm thinking of getting some personal training as I struggle with intense cardio sometimes (legs go to jelly) and I'd like to lose weight and gain muscle. I obviously would like them to have an understanding of h...

12

@Abby_Atkinson

12 Jul 2016 14:42Last reply 14 Jul 2016 15:38

Don't know anyone else with MS...

...so I thought I'd introduce myself here. I was diagnosed in May 2016 (Friday the 13th, lucky me) with relapsing remitting MS after being unable to walk in February and then having severe diplopia and nystagmus in April. The diplopia and the nystagmus are still here nearly three months later, altho...

12

@strawberrygirl

28 Jun 2012 16:33Last reply 29 Jun 2012 07:46

Help wanted!

Hi Guys, I am wondering if anyone can help me? I got diagnosed with relapsing remitting MS 6years ago now and feel I haven't accepted it. I feel like I never have received help with how it effects me emotionally, some days I wish I had never been given the diagnoses of MS as it feels like it plays ...

12

@hhobbs

16 May 2018 19:25Last reply 18 May 2018 02:04

My partner was just diagnosed.

Hello all, My partner was just diagnosed with relapsing remitting MS this year. I am wondering if anyone has any advice on how I can support her. Thank you in advance :)

12

@Nomez

16 Feb 2018 17:40Last reply 22 Jul 2018 13:57

Copaxone and Pregnancy

Hello, I was diagnosed with Relapsing Remitting MS in December last year. It was a bit of a shock but explains the symptoms I have been having over the last couple of years. I had my first meeting with an MS nurse yesterday and we talked through the various DMT options. It would be good to start a f...

12

@Elixir

10 Mar 2021 13:13 EditedLast reply 11 Mar 2021 21:51

Help, newly diagnosed RRMS

Hi there, I've recently been diagnosed with Relapsing/Remitting MS. My Papa (grandfather) had Primary Progressive MS and sadly died 2 years ago, due to UTI complications, which caused seizures and a coma. I first went into hospital in September, after I woke up with severe vertigo, migraine, naus...

12

@Anawith1n

19 Oct 2015 04:31Last reply 20 Oct 2015 04:51

The drug, called Ocrelizumab,

2015UPDATED 13:21, 9 OCT 2015BY JOHN VON RADOWITZ The drug, called Ocrelizumab, is the only known treatment for the disease shown to help one in ten patients A drug is offering hope to sufferers of multiple sclerosis (MS), with experts dubbing it a "game changing" breakthrough. Ocrelizumab has sho...

11