Back in the office after an incredible wedding and honeymoon! Excited to get back to work and use design for positive social change. Need design help? Reach out - abi@abimaydesign.co.uk

It's been a busy couple of months, but I've finally got around to adding some more projects to my website, including the branding for the amazing Young Trustees Movement and a few projects for the MS Society's talented Digital & Content team. https://t.co/GWfx6X8789

Will you be taking part in #MyMSWoof? We'd love to see pictures of your four-legged friends who will be joining you. 📸👇 Once you sign up for the event you'll also receive an MS Society dog bandana to show off yours and your pooches’ achievements, just like Nash, below! 🐕

When you have MS, sometimes it can feel like you start the day on less than zero. This #WorldMentalHealthDay, Jacqueline reflects on her daily life with MS. And how it's always OK to not be OK and ask for help. Find support: https://t.co/Pi0oDhiAAt

Neurology services were neglected long before the pandemic and many people with MS weren’t getting the vital support they needed – now the situation is critical. 📢We need urgent change and #NeurologyNow: https://t.co/NPinC4VHqp

Healthcare professionals are working themselves ragged but still finding it impossible to deliver the care that is needed with the resources available to them. Our #NeurologyNow report shows the tragic effect this situation has on real people: https://t.co/i9nCFH1iqy

Last week, we shared that the @DWP have now released their Health and Disability Green Paper, that proposes changes to disability benefits like PIP. Now the UK Government wants to find out what you think. Share your opinions and #SpeakUpForMS: https://t.co/z070SbLYKl

Sativex, a cannabis-based spray to treat spasms in people with MS when other treatments haven't worked, was approved in England in November 2019. Yet many people with MS are still being denied access - Sativex is only being funded by 46% of local health bodies in England. (1/2)

We’re getting ready for Octopus – our ground breaking multi-arm, multi-stage trial for progressive MS. But how does Octopus work? And what makes it different to other clinical trials? Have a look! 👀📽️ RT and help make Octopus happen: https://t.co/k3FuWN7JjK #StopMS

Here's some of my work from the last year and a bit! To say it was an odd year would be an understatement, never the less I loved working on these projects #graphicdesign #creative #freelancedesign #charitydesign

Too many people with MS in the UK have to fight for the treatments, services, care and support they need. If you’re not getting the services and support you need, taking #LocalActionforMS can change things 📢 Start today ➡ https://t.co/VovxqAiqbt

Do you have a great idea to make a change for people with MS? We can support you to campaign and make it happen! You can still take lots of action online, even during the pandemic. Sign up to be an MS Society campaigner today and take #LocalActionforMS: https://t.co/VovxqAiqbt

It's beginning to look a lot like Quizmas! Just 1 day to go! 🎁 Whether you grab a team from your household or go for it solo, test your festive knowledge and support people living with MS at the same time. 🗓️Wed 9 Dec, 8pm ➡️ https://t.co/7OBR6QFRSa

This International Day of People with Disabilities is about invisible symptoms. When you look OK but that's not how you feel. Watch and share Rebbecca's story to spread awareness of invisible MS symptoms. ➡️ https://t.co/v1vxmvbHnH #NotAllDisabilitiesAreVisible #IDPWD2020

"When my consultant mentioned MS-STAT2 of course I said yes. The way I look at it is, if it doesn’t help me it’s definitely going to help someone else." Andy shares his experience of taking part in our @MsStat2 trial: https://t.co/ATzQI8hDf2 #BehindTheTrials #StopMS

We've been talking about clinical trials. Not everyone can join a clinical trial, but there are more ways to get involved in #MSResearch: 🔸join @UKMSRegister 🔸sign up for our research network 🔸explore our Tissue Bank 🔸take part in a study ➡️ https://t.co/nXIq5qcA78 #StopMS

Meet some of the people behind our @MSstat2 trial: 🔸Dr Anisha Doshi - trainee neurologist 🔸Jacqueline - trial participant (recognise her from our #StopMS TV ad?) 🔸Andy Merry - trial participant and guard at the @TowerOfLondon ➡️ https://t.co/KOPlO2mHOH #StopMS

Will it be 10's all-round in your house-hold? Pub Quiz Live is back tonight! 🔟 Former Strictly contestant and our host, @scott_mills will be asking the Strictly themed questions. 🗓️Weds 28 October, 8pm ➡️YouTube: https://t.co/fqYFFGFH2v ➡️Facebook: https://t.co/AmrMaXlQEq

Thank you to everyone who supported #TooMuchToLose! As the pandemic continues, we can’t allow people with MS to be left behind. Too many people with MS in the UK have to fight for the treatments, services, care and support they need. Let’s take #LocalActionforMS!📢 (1/2)

If you have questions about MS or need any support, our MS Helpline is here to help: 📞 0808 800 8000 ✉️ helpline@mssociety.org.uk