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🔗: bit.ly/4i4fIGW Kevin Sullivan, who lives with arthrogryposis multiplex congenita (AMC), is opening up to PEOPLE about his his day-to-day life. | People
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2020 Arthrogryposis Awareness with AMC Princess Ana - Day 3 - Arthrogryposis is Rare - How Ana feels about being rare - Ana's rare bicycle DONATE to Arthrogryposis Multiplex Congenita Support, Inc. by clicking on the donate button on this post or by going to www.amcsupport.org Want more AMC Princess Ana? You can also find her on: YouTube @amcprincessana Instagram @amcprincessana TikTok @amcprincessana Twitter @amcprincessana | Team AMC Ana
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