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Achondroplasia Support Group
A community of patients, family members and friends dedicated to dealing with Achondroplasia, together.
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08/24/2010 07:07 PM
Beth10
Posts: 1
New Member

My name is Beth and my Grandson was born on May 20, 2010 with Achondroplasia. We have looked at the LPA website and we are very interested in a support group/local chapter with other parents with children with achon.

I think this is crucial and will be very beneficial to my daughter and her husband and all of us. We have yet to connect with other families experiencing the same feelings and experiences with an infant/child with achondroplasia...

If you know of an active and current group in the Plano,Frisco area we would love to hear from you.

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10/06/2010 12:53 PM  Top
jkmurphy
Posts: 1
New Member

Hi Beth my name is Jaime and I am mom to Caitlyn, who is 5 years old and has achondroplasia. I somehow stumbled across this page today and saw your post. I thought that I would send you a message.

Are you or your daughter on Facebook? We have a wonderful group on there called POLP (Parents of Little People). I googled where Plano is and I have several LPA friends in TX. There's a family that lives in Allen, which doesn't look too far from you. Katie has a 3 year old son.

You can email me at jkmurphy@surewest.net

I look forward to hearing from you.

Jaime

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