My name is Jane. I have 3 daughters. My middle daughterrachel (10) was born with Microcephaly. she has melyination issues, slightly large ocpital lobes, thin...
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Jun 1, 2002 7:13 am
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I'm Billy's mom. He is a very hyperactive 5yr old boy. He was diagnosed as microcephalic at about 6months old. He was born with a bifid thumb (now...
Hello, My daughter Rachel was diognose at 5 mounths. She is deaf and globally delayed. She has a behavioral disorder. She is aggressive and self abusive and...
I was surprised to see an answer to my message. Most of the e-mail addresses are out of date. I can't seem to collect my yahoo mail no matter what I try so I...
Hello I just found this group and joined. I am looking to chat with others. Please email me. My daughter is 22 mos old with microcephaly. Thanks Casey...
Hello my name is Malea and I'm Dillon's mom. He's one years old and has microcephaly, cerebral palsy, and seizures. I have my hands full but he is my life!! I...
Rebekah is the youngest of 5 sibs. We were told at birth that she had microcephaly. They gave us the worst prognosis imagined. Rebekah spoke late around 2 1/2...
Hi. The preview of the new Alternatives for Special Kids site can be found at the URL that you have used before, www.4healthykids.org. At the ASK conference,...
Hi. Mr. Alex Sutton, a homeopathic biochemist, is having fantastic success helping kids with severe seizures to be seizure free WITHOUT meds. Let me know if...
Hi - I have just found this sight after 8 months. I am a mum with a beautiful little girl of 14 months named Chiara. She has the longest eyelashes and big...
A note to me from another list: Just wanted to say that I continue to second what Darien has to say about the cell salts... Claire should have intractable...
Lissencephaly / Microcephaly Workshop The Alternatives for Special Kids Conference will have four components: * 200+ 90-minute demonstrations / presentations *...
Kids Wanted for 2003 ASK Microcephaly Calendar Alternatives for Special Kids is looking for children to be a part of its 2003 Calendar series on Microcephaly...
Alternatives for Special Kids is looking for children to be a part of its 2003 Calendar series. These are a collection of calendars that will be sold...
The Alternatives for Special Kids Auctions '03 launch today. Here is an opportunity to support our children and their families in improving their healing,...
Hi i am new to the group and i have a three year old son that has microcephaly. All his doctors have been trying to locate the cause for 2 and a half years. he...
Hi everyone.. I just thought I would tell you a little more about Allison. She is a bugger... She is 12 lbs. and is 251/2 inches long. Her head circ. is...
Hi Valerie How old is Allison? She sounds very similar to Chiara, she is 16 mths now, and her dimensions are similar, (+ very long legs) She isn't quite...
The ASK! workshops offer small group, hands-on interactions with some of the most accomplished expertise in the field. Registrations are limited to 20...
Hi, I'm new to this group. I'm enlisted on another craniosynostosis group and got this email address from one of those moms. My daughter was diagnosed with...
Hi Valerie, I am a grandfather to a beautiful 24 month baby girl who shows no interest in crawling, sitting or using her hands/arms to support herself. My...
Alternatives for Special Kids (ASK!) has a limited amount of scholarships available for its upcoming conference in Irvine, California on May 8 - 11....
im just wanting someone to talk to about microcephaly support group please feel free to email me at tcogley2003@... anytime thank you ... Do you Yahoo!? ...
... hello my name is tonya i just found this group my son is 3 and he has microcephaly also he doesnt say anything which worries me the most and he just...
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