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Arthrogryposis: Questions to ask Neurologist?
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Somya.P
Community managerGood advisor
Somya.P
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Last activity on 10/22/2025 at 7:01 PM
Joined in 2023
775 comments posted | 1 in the Living with conditions affecting the muscles, joints and-or skeleton group
24 of their responses were helpful to members
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Hi @aholcomb,
Thank you so much for sharing! It's wonderful to hear how far your stepdaughter has come, what a strong and determined little girl! 💪 This post may have slipped under the radar for some members, so I’m bringing it back up in case others have thoughts or experiences to share. 😊 Your question is such an important one, and I’m sure many caregivers here have faced similar moments before a specialist appointment.
To help get the conversation going, has anyone else had experience supporting a child with arthrogryposis?
What kinds of questions did you find helpful to ask your neurologist, especially around mobility, motor skills, or future development?
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Feel free to share if you’ve been through something similar, your insights might be just what another member needs to hear today. 💬
Take care,
Somya from the Carenity team 🌼
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aholcomb
aholcomb
Last activity on 09/10/2025 at 5:07 PM
Joined in 2025
Family/friend of a patient with Arthrogryposis multiplex congenita since 2025
1 comment posted | 1 in the Living with conditions affecting the muscles, joints and-or skeleton group
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I have a 7 year old stepdaughter with Arthrogryposis. She has learned to walk with the help of splints and can write beautifully. She just needs help with fine motor skill tasks (buttoning etc). We have a checkup with her neurologist this afternoon. Trying to make a list of questions. Please help!