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Hi, I’m involved with AsianMS (part of the MS Society) and we’re hosting a webinar on Wednesday 9th November 2022 at 6pm UK time. The point of AsianMS is that as well as issues all MSers face, there are also cultural issues specific to the Asian community, but the webinar is open to anyone. Here’s a...

The MS Society is running a webinar on PIP this Thursday 26th January at 6:30pm (in the U.K.) Thought I’d share as I’ve seen a lot of questions about PIP recently. This is the information about the webinar: ‘We’ll be joined by Georgie Wood, an MS Welfare Benefits Advisor from the Disability Law Cen...

https://www.eventbrite.co.uk/e/asian-ms-presents-getting-involved-in-research-participation-and-design-tickets-404720328397 This is the link to sign up to the Asian MS Society Webinar. It will look at MS in different heritages. I would encourage everyone to sign up!!

Hi all, MS expert Professor Gavin Giovannoni aka Prof G from Barts is taking part in this webinar from the ZOE COVID study team (they run the big UK COVID symptom app) talking about vaccines and immunosuppressed people, including MSers. It's going out on 28th October at 3pm but will be on youtube fo...

Spotted this interesting-looking webinar from the British Society for Immunology on "COVID-19 vaccines: how effective are they in people with weakened immune systems?" Might be of interest to some here, especially if you're on an immunosuppressing DMT. https://www.immunology.org/events/covid-19-v...

Hey Team, just wondering if anyone knows of any MS 'webinars' I could participate in? -I'm feeling a little MS lonely lately so would be good to feel more connected. I had participated in the webinars on the MS soc site (anxiety/CV19/RTW) but none avail since end of AUG 2020. I value the support of ...

I watch MS Webinars and MS related videos every night from YouTubers I follow. What are good Webinars you listen to that are regularly updated?’I’m trying to find UK Webinars if possible #webinar

Why is movement so important? 🏃‍♀️🏋️‍♂️ What does it do for your brain, body and mood? 🧘‍♂️🧠 Join MSers Gemma & Susan LIVE this Wednesday as they talk MS, movement & mind health. Sign up here 👉 https://buff.ly/32OqGed

What self-management means to me - Webinar by MS Society, Scotland Free Description Are you living with MS? Do you want to learn more about what it means to self-manage? Join Murray, Anne & Kirsty who will be sharing their experiences and tips on how they live well with MS. When: Monday 1st...

Our very own Grand Fromage @gpeps is on the panel at the MS Academy patient webinar next Monday. All about mental health in MS. - Sign up to take part:- https://multiplesclerosisacademy.org/events/live-webinar-ask-the-experts-mscovid19-mind-health-session-for-msers/

@stumbler hope this is allowed? I've been asked by the MS society to let everyone know about this to give them a chance to join in the webinar , it could be helpful to anyone who is struggling to record a time line of symptoms and triggers for appointments etc. Bullet Journals & Managing MS ...

Hi, For anyone aged 18-35 in the U.K. with MS, there is a new charity specifically designed to help young people. It is called MS Together. There is a website (which will be getting updated soon) and a Facebook group. There are also regional Facebook/WhatsApp groups so you can connect to other young...

Hello. Sorry for the negative post, my first time posting on here! I’m 34, diagnosed with RR MS two years ago and really struggling with the fatigue aspect. I feel like I’m walking through mud everyday, having a shower feels like a huge win and I have no energy to get out or see friends. I’m trying ...

So I am awaiting diagnosis but have seen my mri and gp has confirmed I have ms just awaiting ms team review in October. My problem is my mind is not working like it did. I keep forgetting where I have put things. Cannot remember names/words so get very tongue tied when talking and cannot retain in...

Hi everyone, I am relatively new to MS, diagnosed in 2019, realizing that the struggle is real, i am highly engaged in Facebook groups and my local healthcare MS webinar series but thought it never a bad thing to keep connecting with those around the globe as we are all snowflakes.

Dr Conor Kerley who has had MS for 18y talks with Robert Joyce. Robert is a well-known figure in Ireland and has PPMS. I just discovered there is no need for a linked in account - Zoom it is - https://zoom.us/webinar/register/WN_UCoubSTwQ2aaaF3zksxhtA Or, if you use Linked in already just registe...

I've attended some live sessions before with the ever knowledgeable Dr Boster and they are very informative. Also after the session the Q&A area of the session added to the channel is very active and worth keeping an eye on. Just thought I'd share as I hope to attend ;-) The “down theres” encompa...

If you’ve missed it, we’ve been releasing a video a week as part of a course to help build mental resilience called 'PPE for the Mind'. This week we’re doing things a little differently - join Neuropsychologist Jo and MSer Gemma for a live zoom session, 4pm BST, today (Friday 26th June). Places ar...

I just got a notification of an upcoming webinar from Biogen and couldn't believe who one of the main speakers is. He's a doctor I was seeing for a few years but never really did anything for me. I mean if I'm going to be completely honest I actually got steadily worse while I was seeing him. It was...

These are pretty good webinars (Qatari oil money so all quite spiffy!) From an email I received: << We are very excited to announce that following the success of the last webinar, we will be hosting another online edition of the Education City Speaker Series in collaboration with the World In...