- Home
- Share
- Forum
- Multiple sclerosis Forum
- Living with multiple sclerosis
- MS and the Coronavirus - How are you handling the pandemic?
Patients Multiple sclerosis
MS and the Coronavirus - How are you handling the pandemic?
- 1,718 views
- 49 times supported
- 64 comments
All comments
Go to the last comment
Nathan76
Nathan76
Last activity on 21/11/2021 at 10:40
Joined in 2016
1 comment posted | 1 in the Multiple sclerosis Forum
Rewards
-
Explorer
Any information regarding ms and taking gilyena as I have been on this treatment since October
See the signature
Ntindsley
Desertflower
Desertflower
Last activity on 15/08/2022 at 10:51
Joined in 2017
4 comments posted | 3 in the Multiple sclerosis Forum
Rewards
-
Explorer
-
Evaluator
I only take Low Dose Naltrexone for my MS since 2014. I've been signed off from the Hospital since last year because I don't take any of their Drugs still. I was given permission to self isolate from my job at a school this week. Mainly because I am in contact alot with the students and I could catch the virus. This isolation will be hard for me as I have a Daughter living not far away and 3 Grandsons, but can't physically see them . However we have Facetime at least!
Vixen10000
Vixen10000
Last activity on 20/07/2020 at 10:48
Joined in 2018
1 comment posted | 1 in the Multiple sclerosis Forum
Rewards
-
Explorer
I was diagnosed with MS in 2001. When I was 30 years old I am due to turn 50 in January. My MS is progressing, I am very lucky, I have 2 children, an amazing husband, great family and friend network and a part time job. If anyone is feeling stressed, scared, isolated or uncertain about how you deal with our current challenges, sometimes a chat can help. Please get in touch. Vicki x
See the signature
Vixen
Jomarian
Jomarian
Last activity on 15/09/2024 at 15:05
Joined in 2015
2 comments posted | 1 in the Multiple sclerosis Forum
Rewards
-
Committed
-
Explorer
II'm a retired NHS speech and language therapist, so know little about medical practice, only how to be compliant. i've had MS for 36 years, worked for 12 years after my first symptom but thankfully have not worked since. I've never been at a suitable age for treatment or been advised to have any for MS. For my symptoms since retiring I take modafinil whi GPsch keeps me awake all day and amytriptyline which keeps me asleep at night. I live with my spouse / carer who self isolates better than I do. We both receive PIP and he enjoys shopping on his very able legs. Overall I am lucky in every way and enjoy being at home and making a little money using my laptop. I recommend keeping away from the NHS as much as possible.. When you need help try to talk to GPs by phone, be well prepared with questions and know your own medical history.
See the signature
Jomarian
clarebear030574
Good advisor
clarebear030574
Last activity on 11/05/2020 at 18:46
Joined in 2020
2 comments posted | 2 in the Multiple sclerosis Forum
Rewards
-
Good Advisor
-
Explorer
@Vixen10000 Hi there Vicky, my name's Clare. I'm 45 was diagnosed in 1998 at the ripe old age of 24 and my MS is also progressing and it has been confirmed by my neuro that it has got to Secondary Progressive stage, hardly surprised! lol
I also have 2 children, well 16 and 18 yr old boys so young men! The Hubby buggered off 4 years ago but i do have 2 sons which are in training to do diy (not that the ex used to do it anyway), put the bins out and shopping so no love lost there.
I do have dark moments obviously but I do try to look on the bright side even if this coronavirus is freaking me out a bit!
Anyway, that's enough, just thought I'd say hi and introduce myself.............take care and stay safe, Clare x
ladymary
Good advisor
ladymary
Last activity on 07/08/2023 at 21:39
Joined in 2017
36 comments posted | 27 in the Multiple sclerosis Forum
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Explorer
@Nathan76 @Desertflower @Vixen10000 @Jomarian @clarebear030574 Hello all. I've been self-isolating out of precaution Have any of you received a message from the NHS? The MS Society has a comprehensive page on their site with lots of information and advice. I've been following that since I haven't heard anything yet and I haven't been able to get through to my GP. Stay safe everyone! xx
nameless
Good advisor
nameless
Last activity on 08/06/2023 at 11:50
Joined in 2017
19 comments posted | 18 in the Multiple sclerosis Forum
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Explorer
@ladymary I got a call yesterday. 12 weeks of isolation is it! How is everyone handling the isolation?
LindaBlacker
Good advisor
LindaBlacker
Last activity on 18/12/2024 at 18:32
Joined in 2020
180 comments posted | 71 in the Multiple sclerosis Forum
2 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Committed
-
Explorer
-
Friend
@Vihi everyone my husbxen10000 and abandoned me almost 4yrs ago. Have 1 daughter 3 grandchildren. Was 24yr old when i started with ms symptoms. Its been 39yrs i now have secondary ms. Met my new boyfriend 4 mths ago hes itallian. Hes brilliant about the ms. I self isolate. Scared to death of this dam virus. Hope your all doing well as expected. I live alone life can be daunting. So have to do everything alone. Enjoy the challenge now. Its surprising what you can do when your all alone. Cheers you guys
brianbeecroft
brianbeecroft
Last activity on 30/10/2021 at 19:44
Joined in 2020
1 comment posted | 1 in the Multiple sclerosis Forum
Rewards
-
Explorer
Hi all I'm new to this forum, I have secondary progressive MS, with mobility issues due to my spasticity it my legs. The whole virus issue is a worry, but we carry on regardless.
Carrie16
Carrie16
Last activity on 17/04/2020 at 01:03
Joined in 2020
1 comment posted | 1 in the Multiple sclerosis Forum
Rewards
-
Explorer
Hi all
I’m new to the site, has RRMS since 1983, 2 grown up sons, and a host of delightful grand kids , still fighting and winning so far, so important to stay as positive as we can ( I know it’s hard ) every night I write a wee note, one thing to achieve the next day, sometimes small a walk outside, or a bit of painting indoors, feel great wen I achieve this, if I don’t tomorrow is another day, exercise, fresh air, and rest fills my day, keep safe guys 🧡 Caroline
See the signature
Carrie 16
Give your opinion
Members are also commenting on...
Articles to discover...
04/10/2024 | Advice
Multiple sclerosis (MS) and sexual dysfunction: everything there is to know!
30/05/2024 | News
What are the benefits of herbal medicine for multiple sclerosis?
24/04/2024 | Testimonial
Multiple Sclerosis: “I am a warrior, and I will overcome this illness with love and positivity.”
19/05/2017 | Testimonial
23/03/2018 | News
13/06/2016 | News
02/10/2018 | Advice
Medication fact sheets - patient opinions...
Subscribe
You wish to be notified of new comments
Your subscription has been taken into account
Courtney_J
Community managerGood advisor
Courtney_J
Community manager
Last activity on 13/10/2022 at 16:47
Joined in 2020
1,280 comments posted | 58 in the Multiple sclerosis Forum
10 of their responses were helpful to members
Rewards
Good Advisor
Contributor
Messenger
Committed
Explorer
Evaluator
Hello dear members,
While the Coronavirus epidemic concerns many across the UK (and Carenity members too), I've created this discussion to allow you to talk specifically about the virus in the context of cancer, as we all know that patients can be weakened by their treatments.
Have you had any special instructions from your doctor regarding your care? Are you going to limit your travel? Do you have any advice for others?
Take care,
Courtney