Description
The Adenomyosis Advice Association is working hard on this year's Rare Disease Day 2021 campaign and in this our 10th year of the Association, we have been invited by My City Med to take part in '24 Hours of Rare: A Global Celebration' on 28th February 2021. The Adenomyosis Advice Association will act as a resource and as a leader in the rare disease global community. The event will be full of excellent content and information and will go live across the globe to organisations highlighting rare diseases. The event will be free to all patients and caregivers - so look out for more information on our social media pages and please share, not only to raise the adenomyosis awareness campaign further, but to hightlight what is set to be a fantastic event!
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