#relapsing-remitting

24 Sep 2015 13:50Last reply 5 Mar 2021 16:41

Best Treatment for Relapsing Remitting

I am a 25 year old man from Ireland. I was diagnosed with Relapsing Remitting MS in September 2015. I have been six treatments to choose from 1) Tecfidera 2) Plegridy 3) Avonex 4) Rebif 5)Copaxone 6) Betaferon. If anybody is on any of these and has any advice or recommendations I would be delighted ...

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@gpeps

25 Mar 2013 18:44Last reply 17 Feb 2021 22:00

From Relapsing Remitting MS to Secondary Progressive - questions please!

Hi all, We've got Prof Alan Thompson from the Institute of Neurology in London lined up to respond to your questions about the transition from Relapsing Remitting MS to Secondary Progressive MS. Professor Thompson is a world leader when it comes to progressive MS and this is your chance to ask...

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@Ladianna

14 Feb 2021 18:16Last reply 15 Feb 2021 09:10

Hi my name is Anne and I have relapsing remitting MS for 23 years.

I’m having difficulty with my fatigue I was on provigal and know I’m on Ritalin. I’m going to be trying a time release Ritalin. Ugh. I want aderall. I have done my research. I’m terribly frustrated . I live in Erie Pennsylvania.

3

@Michelle_Grimstad

6 Dec 2019 20:07Last reply 7 Dec 2019 13:57

My relapsing remitting ms

I've had ms for 18 yrs now got diagnosed when I was 27 im on tysabri excellent med I haven't had a relapse for about 10 yrs since I started it but if anyone has any questions I will trt and help I walk still just can't walk for long distance like walmart for that I use my manual wheelchair I'm prett...

3

@Octavio_Breme

6 Dec 2019 09:00Last reply 7 Dec 2019 05:08

Relapsing remitting MS (Tier 2 Visa)

Good morning, I´m from Argentina and I have relapsing remitting MS since 2010 aprox. My employee has offered a job in the UK to start in February and they are requesting a Tier 2 Visa for me and my wife, we need to pay for the Healthcare Surcharge. Right now I´m taking Gilenya Fingolimod 0,5mg; do y...

2

@nicolesmiles

12 Aug 2019 07:37Last reply 12 Aug 2019 08:52

25 Perth, relapsing remitting.

Anyone have experience taking modafinil?

1

@yesterdaysgal

3 May 2017 03:37Last reply 5 May 2017 06:09

Relapsing, Remitting

Temporary memory loss is common for me. I try to stay positive. As a great post once said; Never admit to having an illness. Unfortunately the lack of admission only works when you feel good.

2

@supersmileygal

7 Jul 2009 13:24Last reply 7 Jul 2009 13:24

Relapsing-remitting

I was only recently diagnosed with MS and found to have this form, and must admit that I'm finding it hard to come to terms with. Does anyone know of any counselling support through the NHS that can help with this? e.g. MS nurses etc?

8

@JMon

26 Nov 2022 16:56Last reply 26 Nov 2022 17:03

Newly confirmed , type?

Hey All just confirmed MS in September via MRI & Lumbar puncture. I am wondering how long did it take for your diagnoses to be specify into type . Relapsing Remitting MS. Primary Progressive MS. Secondary Progressive MS.

Galway, Ireland

1

@Chezza1

23 Nov 2022 13:46 EditedLast reply 23 Nov 2022 18:40

My MS story

My symptoms started in December 2019, when my left hand wasn’t doing what I wanted it to do, fast forward to now after 8 MRI scans, 2 lumber punctures, 2 VER and 1 EMG. Also two weeks in hospital with numerous neurologist assessing me. I was diagnosed in February 2022 with relapsing remitting MS, a ...

2

@Amyla72

16 Nov 2022 10:27

@Amyla72

Diagnosed in 2004, relapsing/remitting & trudging along one day at a time since. Seventeen years strong 💪🏻 & still kicking!!

Beverly, United States

@VioletRose88

4 Nov 2022 21:10Last reply 15 Nov 2022 11:47

How long have people been on Tecfidera for?

Hi everyone, I had Relapsing Remitting MS since 2018 and diagnosed in early 2019. I have been on Tecfidera since March 2019 and been on it ever since so almost 4 years. What is the longest people have been on Tecfidera?

39

@Keke

24 Apr 2022 19:25Last reply 15 Nov 2022 04:45

Newly diagnosed

Hi all, I was diagnosed with relapsing remitting in December of 2021. Feeling a bit abandoned after going through so many appointments and tests last winter to checking in once or twice a year going forward. I am on Ocrevus, next infusion is in August. I am grateful for the appointments and care ...

Northfield, MN, USA

10

@Jessicac

1 Nov 2022 12:44Last reply 13 Nov 2022 21:20

Tingly feeling after Ocrevus infusion

Hi, I have recently been diagnosed with Relapsing Remitting MS and have had my first dose of Ocrevus, receiving my next dose this Friday. I just wondered if anyone after theirs had a really strange tingly feeling in their face and limbs after having it? I haven’t spoken to my MS nurse yet but I’m th...

2

@Wuchick

29 Sep 2022 23:57 EditedLast reply 12 Nov 2022 20:53

MS and pregnancy

Hi everyone, I'm new here and happy to be a part of the community. @ 33 weeks pregnant, with relapsing remitting MS, wondering if anyone here has anything to share about labour, post partum and MS. I've been told by my nuerologist that an elective cesarean isn't necessary unless otherwise advised by...

2

@Sheltielove

12 Nov 2022 12:25Last reply 12 Nov 2022 20:40

Optic neuritis and other eye issues

Hello there, Decided to reach out because I am at a crossroads. Diagnosed with relapsing remitting MS in 1998 and started Avonex that same year. Been on Avonex Ever since. Over the last 10 years my MS has remained stable with some noticeable weakness in my legs since the pandemic, I contribute that ...

3

@OrianaP

12 Nov 2022 12:31

Anxiety and feeling of loss

Hello ! My name is Oriana, I am from Spain and I am 23 years old.. I have sm relapsing remitting . I was diagnosed in August and since then I have been between vaccines and treatments. Since I found out I have felt anxious and with many mood swings, any advice on this

@Lindsay25

10 Nov 2022 03:28Last reply 11 Nov 2022 06:48

Does anyone else have both MS and IIH?!?

Hey everyone! I live in Southern Illinois. My problem started in October 2021 with eye problems. I was having moments of blindness. My optometrist discovered that my optic nerves were incredibly swollen. He referred me to a neurologist. After all the MRI’s, blood work, and lumbar puncture, my neurol...

2

@Doug_Graham

12 Nov 2021 15:35Last reply 2 Nov 2022 12:38

Pilates has improved my core strength & ability to walk

I spent 20 years in the US Navy. I had a passion for exercise and distance running. Before I retired in 1995 I became aware of new difficulty running and began to have developing eye problems. In 2002 I was finally diagnosed to have Relapsing / Remitting MS. By then I was an Engineering Manager fo...

Colleyville, TX, USA

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@HeidiHelps

1 Nov 2022 19:39Last reply 1 Nov 2022 23:31

Alzheimer's Disease and MS

Yes, it's possible to have MS and dementia, such as Alzheimer's disease. Changes to the brain can be caused by both MS and Alzheimer's disease. People with relapsing-remitting MS, primary progressive MS, secondary progressive MS, and even very mild MS can go on to develop Alzheimer's disease too. Al...

Kamloops, Canada

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