In partnership with @NeuroAlliance, today we’re launching a new tool designed to help NHS commissioners, providers & professionals to plan, design & improve local services for people of all ages affected by headache and migraine.
Read more about the tool: https://t.co/LrTeDf47cA
@MigraineTrust wants to learn about your experience in accessing migraine treatments. We want to ensure anyone living with migraine has fair access to treatment and care. If you're aged 18+ and live within the UK, please consider completing our survey: ➡️ https://t.co/8E7hUAy3DT
Earlier this week Lord Londesborough @UKHouseofLords raised the need for improved migraine care, and why the government must consider migraine as part of key conversations around work and health - catch up here: https://t.co/S7JqRZOpWQ
🎄Our helpline elves are in need of a well-earned break this festive season!
📞Our helpline & live chat will be closed from 4pm 23 Dec, reopening 10am Friday 2 Jan.
You can email, fill in the Live Chat form & leave a message & the team will get back to you in the new year.
Recently, Maria spoke with @WebMD about the impact of migraine on her life, the validation that came from diagnosis and developing her own strategies for managing life with migraine. Check out the video here 👇
https://t.co/qe4XplkZjZ
Who we are affects how we experience migraine. Aspects like gender, ethnicity and social background can influence the way we talk about, and seek support for, migraine. Our new research explores how inequities shape migraine experience: https://t.co/mdzNqFyhWf
Every contribution, big or small towards our £21,300 donation target will help us to invest in real-life research with people affected by migraine, so that we can help them access better treatment, feel understood and live fuller lives 💙
1)From today until Tuesday 9 December, all donations made to The Migraine Trust via the #BigGiveChoice#ChristmasChallenge website will be doubled at no extra cost to you: https://t.co/UY4HHAxNyD One donation, twice the impact!🌟
We need your vote! 🗳️✅ Our 'Migraine Means' campaign film is up for a @SmileyCFA award! Please take a moment to vote for it here: https://t.co/WdIO10emkQ
🎙️ Fantastic conversations with @PJOnline_News on their most recent PJ Pod episode around the important role of pharmacists in contributing to better migraine care. Check out the episode here👇
In our latest #PJPod episode, we discuss insights from a recent expert roundtable, which explored how pharmacists can contribute to improved migraine care for patients and optimise the use of medications
#migraine#ukpharmacy#communitypharmacy
https://t.co/QquTeW5Y1H
Our Information and Support Services team are ready to answer your questions! From treatment options to your rights, you can submit anonymous questions here and we will answer as many as we can in a video coming to our social channels on 11 December.
https://t.co/ZJpYXwVoGT
This week, we joined fellow @NINCA_NI members to call for urgent changes to neurology services in NI. Find out more about the #FightForNeuro campaign & what it means for people with migraine living in Northern Ireland:
https://t.co/60ITCghGPZ
We’re here today at Stormont for the @NINCA_NI#FightForNeuro campaign launch, calling on the health minister for improved access and better investment in neurological care in NI
Join us on 3 November for our next Managing Your Migraine as we hear from Susie Lagrata – Advanced Headache Nurse Practitioner – about lifestyle and non-drug treatments in the self-management of migraine
Book your free place here:
https://t.co/n2hApc3aL4
Thanks to Sean for helping to raise awareness of the experiences of people with migraine in the workplace and the change that we need to see.
You can read more about Sean’s experience here: https://t.co/DpLsrjQ4QP
Our research shows that Sean isn’t alone in his experiences with 91% of people living with migraine working while experiencing migraine symptoms. 65% of people with migraine felt that others often don’t believe them when they report their symptoms.