NottinghamMSSociety

Nottinghamshire & District MS Society here to support people with MS and their friends & families.

[Disability Rights UK @DisRightsUK]

London is failing to make itself more accessible for those with disabilities: https://t.co/l48jGv7beF

[NottinghamMSSociety @nottingham_ms]

Disability inclusion is good for the environment – or it could be… https://t.co/QFI4p2juvQ

[MS Society UK @mssocietyuk]

Only 3 days to go! Thank you to everyone who has signed our letter calling on UK governments for urgent change and #NeurologyNow. If you haven't done so, please join us: https://t.co/NPinC5dihX

Help us spread the word - RT and share our open letter far and wide! #NeurologyNow

[NottinghamMSSociety @nottingham_ms]

Employment and reasonable adjustments - Find out about what support might be available to you or your employer following your MS diagnosis while in employment. https://t.co/Rmk7IsPiw4 via @mssocietyuk

[NottinghamMSSociety @nottingham_ms]

Information webinar - my changing MS symptoms - Are you living with MS? Are your symptoms changing? You’re not alone. https://t.co/7dIDNfPK5l via @mssocietyuk

[NottinghamMSSociety @nottingham_ms]

Menopause and MS webinar - Dr Laura Jarvis, together with a volunteer with lived experience, will lead this interactive webinar on how menopause affects MS. https://t.co/jSco0lkUtS via @mssocietyuk

[NottinghamMSSociety @nottingham_ms]

Mindfulness and meditation webinar - Join award winning wellbeing coach Donna Booth for a session all about the benefits of mindfulness for anyone affected by MS. https://t.co/wirQ98L2vs via @mssocietyuk

[christina applegate @1capplegate]

Hi friends. A few months ago I was diagnosed with MS. It’s been a strange journey. But I have been so supported by people that I know who also have this condition. It’s been a tough road. But as we all know, the road keeps going. Unless some asshole blocks it.

[christina applegate @1capplegate]

As one of my friends that has MS said “ we wake up and take the indicated action”. And that’s what I do. So now I ask for privacy. As I go through this thing. Thank you xo

[MS Society UK @mssocietyuk]

The Prime Minister promised to 'fix social care' and he must keep his word and deliver for the millions of older and disabled people of working age and their carers.

Email your MP and ask them to act now: https://t.co/skZDrLtvOL #KeepYourPromiseBoris

[MS Society UK @mssocietyuk]

It’s easy to get caught up in our thoughts and worries. Whether it's #FridayThoughts. And Saturday thoughts. And Sunday thoughts...

It's important to look after your mental health. If you're experiencing stress, our info may help: https://t.co/EdMRWg15lE #StressAwarenessMonth

[Shift.ms @shiftms]

Very hopeful article from @MSNewsToday

A machine learning-based method that examines walking abnormalities in people with MS could help identify patients who are at high risk of worsening symptoms, a study suggests. 🙌 💚

Read the full article here 👉 https://t.co/teLwmEtbnz

[MS Society Scotland @mssocietyscot]

This MS Week (19-25 April) #LetsTalkMS and raise awareness.

We want to help others better understand MS, and some of the challenges it presents.

Complete our survey and help us to raise awareness about living with MS: https://t.co/Sp8Hyrqcgl

[MS Society UK @mssocietyuk]

Did you know that April is #StressAwarenessMonth? People with MS often find that stress impacts on their condition in some way.

It's important to look after your mental health. If you're experiencing stress, our information and tips may help: https://t.co/EdMRWg15lE

[MS Society Scotland @mssocietyscot]

Has someone you’re close to been diagnosed with MS?

This month join our online Friends and Family Wellbeing sessions to learn more about living well and different ways you can support your loved one to manage their MS.

👉 Sessions begin 22 April: https://t.co/RHqTsTFFLY

[The Institute of Mental Health @InstituteMH]

*New study*
Have you found it difficult to return to work / education after MS or Covid-19?
Why not take part in our online survey?
We'd also like to hear from 'healthy volunteers' - click on the link for more info.
@arc_em @NEuRoMSproject
https://t.co/aT1t3tAt6j

[MS Society Scotland @mssocietyscot]

This #MSAwarenessWeek (19-25 April) we want to help others better understand MS.

#LetsTalkMS and some of the challenges it presents.

Complete our survey by 29 March, and help raise awareness about living with MS: https://t.co/miM8XCniQF

[Shift.ms @shiftms]

What are things you discovered about your MS / Your life with MS due to lockdown?
- For me it was the impact the open plan office had on my energy levels
- How much healthcare could be done over the phone

[MyMSTeam @MyMSTeam]

Members of MyMSTeam admit that they say "I'm Fine" when they're NOT because most people don't understand life with #multiplesclerosis. Why do you say it? Share in the discussion: https://t.co/A35wgqAAjk

[MS Society Scotland @mssocietyscot]

Fatigue is one of the most common symptoms of MS.

If you’d like to learn more about ways that can help manage your energy levels and prioritise the activities that you value most, join our Fatigue and my MS webinar.

🗓️ 18 March, 7pm
➡️ https://t.co/0CS5ALdA3X