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Come check out Let's Talk Achondroplasia!
Hi, friends!
Have you seen The Mighty’s newest group?
We recently launched Let’s Talk Achondroplasia, a public group for peer support and connection around achondroplasia (ACH), the most common type of dwarfism. Whether you have been diagnosed with ACH, care for someone else who’s been diagnosed, or you are an ACH patient advocate or educator, our community is here to support you!
Join us here: Let’s Talk Achondroplasia
#LetsTalkAchondroplasia #LivingWithRareDisease #RareDisease #Achondroplasia #MightyTogether
Let’s Talk Achondroplasia | An Online Health Community
We know how hard it can be to get answers and find connection with a rare disease. This is a public group where you can connect with others affected by achondroplasia (ACH), the most common cause of short stature, or dwarfism. Whether you care for someone diagnosed with achondroplasia, you are diagnosed with the condition yourself, or you are an ACH patient advocate or educator, we are here to support you! In this group, you can chat freely about your experiences, discover resources and events, and find peer support along your achondroplasia journey.
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