Hey everyone.

Jacqulynn - posted on 08/09/2009 ( 3 moms have responded )

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I am glad to see the Group has gotten 546 mommies in here. See everyone we may feel alone but we don't need to. There are many other moms with stories and children just as special as our own. It's like we are our own family in here. With not only just the birth injuries but the many complications that can come to a child during or shortly after the birth we always need to remember that we are never alone we have our internet family here to help us through our rough times and hopefully hear about our good times. I am very glad that our community has been so open to exchange stories about themselves and their experiences with their always handsome/beautiful children. And remember my friends we are never alone.

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Emma - posted on 03/03/2011

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Hi my name is Emma, my son will be 2 in May. I had a severe shoulder dystocia delivery with him. He had HIE and erb's palsy. He has made a good recovery from erb's palsy. He has low muscle tone, lax ligaments, mobile joints. poor spacial awareness and is very hyperactive. We have yet to get a diagnosis but have been told he may have cerebral palsy. Anyone else have a child/children with the same problems?

Rose - posted on 02/16/2010

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Hi, my name is Rose and my daughter Allyson is 3 yrs old. She was born with erbs palsey. It would be very helpful to talk to other parents with or children with erbs palsey.

Lesley - posted on 10/07/2009

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hi there my name is lesley my little age is 8 and has quad, cerebral palsy i would love to talk to other parents who children have c.p x