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  • Profile picture of Brittany Pittman
Group logo of Cerebral Palsy and Hydrocephalus

Cerebral Palsy and Hydrocephalus

Public Group active 10 months, 3 weeks ago ago

My daughter has both. I am interested in talking with other parents who have a child or children with one or both of these. Anyone is welcome to join to put their own opinions, facts or ask questions.

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  • Profile picture of m

    m joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 10 months, 3 weeks ago

  • Profile picture of Jennifer Giroux

    Jennifer Giroux posted an update in the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 4 months ago

    My daughter is 10 years old and was diagnosed with hydrocephalus at 18 months, shunted at 19 months. She is on an IEP at school and receives speech and occcupational therapy at school, pull out for math and push in for language arts. She is a pretty happy girl but really wants to have some friends.

  • Profile picture of Jennifer Giroux

    Jennifer Giroux joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 4 months ago

  • Profile picture of Tammy Giardina

    Tammy Giardina posted an update in the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus: 1 year, 6 months ago

    I have an 8 year old son who wears an AFO on his right foot. The latest one he received is a bit bulky. I have heard on the CP/Hemiplegia list serve I read occasionally that the Croc’s brand shoes are good. Does anyone have any experience with this?

    • Profile picture of Julia Roberts
      Julia Roberts replied 1 year, 6 months ago · ·

      Tammy, when our daughter had them we went to get her fitted for a pair of shoes…there were a few brands that run wider. Crocs wouldn’t have worked for our girl because she lacked (and still does) the toe strength to keep shoes like that on her feet and trips too much. She JUST this past summer started wearing flipflops, although she’s worn…[Read more]

    • Profile picture of Sylvia Ross
      Sylvia Ross replied 1 year, 6 months ago · ·

      Micah can’t do Crocs either. We love Keens hiking style shoes. I get them from zappos.com (free shipping both ways if you want to try a couple of different sizes to see what she needs). The insoles were easy to remove to allow extra depth for his AFOs.

    • Profile picture of Jennifer Giroux
      Jennifer Giroux replied 1 year, 4 months ago · ·

      Claire used to wear AFO’s in her shoes and we found that Stride Rite x-tra wide shoes worked best. They are a little expensive, but gave her solid support. Crocs do not work for her, as much as she would like them to. They just don’t offer enough support.

  • Profile picture of Tammy Giardina

    Tammy Giardina joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 6 months ago

  • Profile picture of Laurie

    Laurie joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 7 months ago

  • Profile picture of Jean Schroeder

    Jean Schroeder joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 8 months ago

  • Profile picture of Erin

    Erin joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 9 months ago

  • Profile picture of CJ

    CJ joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 9 months ago

  • Profile picture of Courtney

    Courtney joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 1 year, 11 months ago

  • Profile picture of Shelley Mannell

    Shelley Mannell posted an update in the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus: 2 years ago

    study in Experimental Brain Research journal in 2010 indicates that children with spastic CP have more difficulty with sitting balance with their eyes closed (not so for children with dyskinetic CP). These children may be using their eyes to reinforce their balance which may interfere with their ability to use their eyes for reading. Ask your PT!

    • Profile picture of Michelle Howard
      Michelle Howard replied 2 years ago · ·

      Very interesting. My son has spastic cp and has trouble sitting steady with his eyes open!

  • Profile picture of Shelley Mannell

    Shelley Mannell joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 2 years ago

  • Profile picture of Colleen Pohl-Weary

    Colleen Pohl-Weary posted an update in the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus: 2 years ago

    A specialist I took my 2 year old son to suggested that he has slight spasticity in his lower legs, Babinski’s reflex, and had some white matter brain damage in his deep brain white matter. He called it a static encephalopathy. No one has yet called it Cerebral Palsy, but I’m pretty sure that would explain why he stumbles over one leg all the…[Read more]

  • Profile picture of Colleen Pohl-Weary

    Colleen Pohl-Weary joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 2 years ago

  • Profile picture of Tubaville

    Tubaville joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 2 years ago

  • Profile picture of M_B

    Marla_B posted an update in the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus: 2 years ago

    I didn’t realize this group existed until just now. My daughter has what has been classified as mild athetoid/dystonic CP. (She doesn’t seem to actually have dystonia, but the neurologist used that term so for now I use it too.) Hello!

  • Profile picture of M_B

    Marla_B joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 2 years ago

  • Profile picture of Oceana

    Julie Vila joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 2 years ago

  • Profile picture of Ruth Nelson

    Ruth Nelson posted an update in the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus: 2 years, 1 month ago

    I have a son with both as well. However his Hydrocephalus has been considered benign and he has been released from that specialist!!

  • Profile picture of Ruth Nelson

    Ruth Nelson joined the group Group logo of Cerebral Palsy and HydrocephalusCerebral Palsy and Hydrocephalus 2 years, 1 month ago

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  • Cindy Marie commented on the blog post Four Things That Stifle Caregivers and Kill Their Dreams 1 day ago

    This is such a powerful article that I am sharing with my best friend. She has a special needs child and has a lot of tunnel vision about herself. I try to explain things to her such as these four examples but I […]

  • Profile picture

    Blog: Trivia Thursdays (No. 3- Answer and Winner) from Sailling Autistic Seas in the group Group logo of Blogging Our LivesBlogging Our Lives 1 day, 1 hour ago

    Yesterday’s Trivia Question was: What year was the word “autism” first added to the Diagnostic and Statistical Manual of Mental Disorders (DSM)? Answer: 1980 For […]

  • Profile picture of Justin Hennessey

    Justin Hennessey became a registered member 1 day, 3 hours ago

  • Profile picture

    Blog: Trivia Thursdays (No. 3) from Sailling Autistic Seas in the group Group logo of Blogging Our LivesBlogging Our Lives 2 days ago

    Every Thursday, I will ask a trivia question. The questions will fall under developmental disabilities, special needs parenting, special education, etc. Any week […]

  • Carol Davis Costin commented on the blog post Surrounded by the love of a public school. 2 days, 12 hours ago

    Julia, for the second time today, you made me cry. The video was the first time. Thank you for this. Sean is not a special needs child but we certainly feel the same you do about the school and the people in it.

  • Profile picture of Julia Roberts

    Julia Roberts commented on the post, For better or worse. Or worse., on the site Kidneys and Eyes 2 days, 15 hours ago

    I completely understand…because, let’s face it, the kids health surrounds everything we do. As far as lessons, well, a lot of it we just make up as we go along.

  • Profile picture of Julia Roberts

    Julia Roberts commented on the post, For better or worse. Or worse., on the site Kidneys and Eyes 2 days, 15 hours ago

    Awww, thanks. But it’s really Julian.

  • Profile picture of Jenny smith

    Jenny smith became a registered member 2 days, 17 hours ago

  • Deenie commented on the blog post For better or worse. Or worse. 2 days, 22 hours ago

    I kind of feel weird saying that I loved this post since so much of it was about your kids fragile health … but I did. A lot of people could take lessons from you guys.

  • 20% Project: Day Two | emily the educator commented on the blog post Squag: Connecting Kids with Autism through Social Networking 2 days, 22 hours ago

    [...] * http://supportforspecialneeds.com/2010/10/14/squag-connecting-kids-with-autism-through-social-networ… [...]

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  • 20% Project: Day Two | emily the educator on Squag: Connecting Kids with Autism through Social Networking
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