Learn how #plasmaprotein therapies have helped people who live with rare diseases, like Ed, live healthier lives.http://bit.ly/32nNwZ3.

We are the 30 Million people asking for a EU Action Plan for Rare Diseases to

✅ Improve the quality of people living with a rare disease
✅ Extend their life expectancy
✅ Establish Europe as a world leader in #raredisease therapies

👉 http://l.eurordis.org/EMM #30millionreasons

Any action which speaks in favour of, recommends, argues for a cause, supports, defends, or leads on behalf of others is ADVOCACY. Check out the progress on the Alpha1 #AdvocacyPathway

Many individuals with rare and genetic disorders rely on you for their #plasma therapies, especially now as we continue to face reduced donations due to #COVID19. Find a donation center near you: http://donatingplasma.org.

#PlasmaDonorsSaveLives 💛

As part of Stress Awareness month ... how do you manage your stress and emotions? Have you ever use the 1-2-3 technique ? Find out more on http://www.facebook.com/alpha1.org.uk/
#a1uksupport #selfcareisntselfish #mentalhealthawareness #StressAwarenessMonth

We're counting down the days until the 2021 Virtual Alpha-1 National Conference in June! Show us you're "All in for Alpha-1" by registering early here: http://a1f.org/alpha1conference

There are 3 days left until our policy event on Improving Care for Alpha-1 Patients. Register today to listen to Alpha-1 experts, patients, and Members of European Parliament discuss ways to improve care for Alpha-1 patients!

Register here: http://ow.ly/Aqpv50Etbhn