SMile

🇷🇴 Counseling and support group for people with MS/ //

[SMile @CentrulSMile]

@ConorKerley Great job with your presentation at the Romanian conference!🙌

[Shift.ms @shiftms]

Cognitive impairment is one of the most common hidden symptoms of MS 🤔🌫️ but there are things you can do to keep your brain working at it’s best and mitigate the symptoms.

Check out our 'Ways to keep your brain active' blog by Sarah here ➡️ https://t.co/5k11eFCGU6

[MSTrust @MSTrust]

If you are newly diagnosed with MS and experiencing relapses, you may be considering treatment with a disease modifying drug.

This short guide explores the range of drugs available that can decrease the number and severity of relapses.

https://t.co/9m6jvpXTLY

[MS Society Scotland @mssocietyscot]

BREAKING NEWS | Siponimod, a new treatment for secondary progressive MS, has been approved for use on NHS Scotland.

It's the first oral treatment to be made available on the NHS in Scotland for secondary progressive MS.

[SMile @CentrulSMile]

@shiftms Hi, Oana! Have a great Takeover weekend! Hugs from Cluj!! 🤗

[SMile @CentrulSMile]

Important for #Msers who use(d) interferon-beta!

[WHS Alumnae @whsalumnae]

Please support WHS Alumnae @TrishnaBharadia who was diagnosed with MS 12 years ago raise money for @mssocietyuk All donations greatly received #StopMS #mswalklive #WycHighProud #ThisWHSGirlCan

[SMile @CentrulSMile]

Most #MSPatients struggle with these thoughts

[OZ @OZbipp]

https://t.co/AB3bKVCSWY

[Shift.ms @shiftms]

"My experience of using cannabis as an alternative to using prescribed drugs to aid my MS symptoms."

Check out Paul's guest blog here 👉 https://t.co/LKf1DEDhrU

[SMile @CentrulSMile]

Patients might not have a similar professional background as HCPs, but nobody knows more about the MS bodies/symptoms/struggles than the #MSpatient! And no one else can fully understand! So who’s really the expert on #YourMS?

[Trishna Bharadia BA(hons), MFPM(hon) @TrishnaBharadia]

Just heard someone refer to Patients & Carers as not being experts. Apparently if you're a scientist, physician, pharmacist or work in pharma, you're an expert. But if you're a patient or caregiver you're a "non-expert." Really??? At the very least we are experts in

[Shift.ms @shiftms]

Misunderstanding of MS is common, often family members, friends & others who we love just don't get it 😕🤷‍♀️

But how can we expect them to get it when we don't talk about MS?

Sidecar is a film exploring the pressures of advanced MS. Watch ➡️ https://t.co/h1MaD1iU3I

[Shift.ms @shiftms]

VOTE for us to win ➡️ https://t.co/0oRTLDf6cn

We're so happy to see our 'Animated Symptoms' series has been nominated by
@Webfestberlin 🤗 The series shows real stories & experiences told by people living with symptoms of #MultipleSclerosis.

[WebMD @WebMD]

Studies are beginning to show that, in rare cases, people with severe COVID-19 may develop the serious nervous system disorder known as Guillain-Barre syndrome. What to know: https://t.co/8bJsDk3lks

[European MS Platform @eumsplatform]

Did you miss the ’You Have MS: Why every word counts’ webinar 👨‍🏫💻last Wednesday on the impact of communication🗣 between people with #MS and their HCPs?

The recording is now available here: https://t.co/9MAjiMPY74

#EMSP2020 @MS21Century

[Birgit Bauer @Birgitpower]

Sitting with the great Steering Committee of @MS21Century online together in our spring conference. We all #stayathome but it is great to see the people online and move #ms21 forward! #ms

[European MS Platform @eumsplatform]

It is with great sadness that we decided to postpone the EMSP conference to the end of November 2020.

This decision was required to protect our community from exposing themselves to any risk during the current COVID-19 outbreak.

For more info👉 https://t.co/XmEoitbL9z

[Trishna Bharadia BA(hons), MFPM(hon) @TrishnaBharadia]

“Coronavirus & MS”
I have compiled a list of reliable sources of info & links so PwMS can make informed decisions regarding treatment & actions. Includes ⁦@MSTrust⁩ ⁦@mssocietyuk⁩ ⁦@BartsMSBlog⁩ ⁦@AaronBosterMD⁩ ⁦@MSUK6⁩ https://t.co/ZtQ3GJoVoX

[MS Society UK @mssocietyuk]

We’ve been talking to lots of people in our community about MS and #COVID19.

We answered some of the questions that crop up the most: https://t.co/ynfPf5xoAa #ukcoronavirus #coronavirus

We're regularly reviewing and updating our information, so keep checking in with us.

[European MS Platform @eumsplatform]

Happy International Women's Day! Today we're celebrating all the amazing women in the #MS community!

Who are the inspirational women in your life? Reply below, we'd love to hear from you!
#HappyWomensDay2020 #InternationalWomensDay #IWD2020

[European MS Platform @eumsplatform]

Help @MS21Century to understand your perspective on the influence of families and carers on decision-making and appointment satisfaction of people affected by #MS #MS21

📝 Share your experiences by taking 2 minutes and filling their survey: https://t.co/T2Nj8iMd6z