Description
This year on Rare Disease Day the Adenomyosis Advice Association will be focusing on future research opportunities and how with the support of our trusted partners at Westminster, across the UK’s NHS and associated research bodies, the Association is at the forefront of understanding the impacts of COVID on adenomyosis patients worldwide and is actively supporting and ensuring that patients receive the support they need.
The Adenomyosis Advice Association’s event in association with the EURORDIS – Rare Diseases Europe Rare Disease Day 2022 campaign will continue across the whole weekend from Friday 25th to Monday 28th February.
In this our 11th year of the Association, we will also highlight adenomyosis stories in the media worldwide and will share all of the above on our website and associated media platforms. We invite Association members, their families and friends to actively take part by sharing our updates, so please feel free to join our awareness campaign on Rare Disease Day 2022.
Many thanks for your support.
Danielle
Founder, Adenomyosis Advice Association
www.adenomyosisadviceassociation.org
#ADENOMYOSISAWARENESS #RAREDISEASEDAY
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