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Microcephaly - Foundation for Children with Microcephaly

Welcome to the Foundation for Children with Microcephaly! We have created this website. To help and inform parents and families of children who have been diagnosed with. Microcephaly, Lissencephaly, Polymicrogyria and other closely related neurological. If your child has just been diagnosed, you have a million questions and thoughts running. Through your head. It gets really frustrating when no one has the answers to any of your. Questions. We are here to help! Contact a parent now. Just try to help our ...

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Microcephaly - Foundation for Children with Microcephaly | microcephaly.org Reviews

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Welcome to the Foundation for Children with Microcephaly! We have created this website. To help and inform parents and families of children who have been diagnosed with. Microcephaly, Lissencephaly, Polymicrogyria and other closely related neurological. If your child has just been diagnosed, you have a million questions and thoughts running. Through your head. It gets really frustrating when no one has the answers to any of your. Questions. We are here to help! Contact a parent now. Just try to help our ...

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Microcephaly - Foundation for Children with Microcephaly | microcephaly.org Reviews

https://microcephaly.org

Welcome to the Foundation for Children with Microcephaly! We have created this website. To help and inform parents and families of children who have been diagnosed with. Microcephaly, Lissencephaly, Polymicrogyria and other closely related neurological. If your child has just been diagnosed, you have a million questions and thoughts running. Through your head. It gets really frustrating when no one has the answers to any of your. Questions. We are here to help! Contact a parent now. Just try to help our ...

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microcephaly.org

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Foundation for Children with Microcephaly - Volunteer

http://www.microcephaly.org/volunteer.html

Disclaimer: The information provided on this website is to inform and help new parents cope with the sudden, unexpected change in their life. The. Information contained on this site is not intended to replace information you have received from doctors or other health professionals. Though there are. Many facts on this website, there are also many opinions. We are not doctors, we are parents with children diagnosed with Microcephaly. A Message from the Founder:. Time, effort and hard work!

2

Foundation for Children with Microcephaly - Donate - Little Help... BIG Difference

http://www.microcephaly.org/donations.html

Disclaimer: The information provided on this website is to inform and help new parents cope with the sudden, unexpected change in their life. The. Information contained on this site is not intended to replace information you have received from doctors or other health professionals. Though there are. Many facts on this website, there are also many opinions. We are not doctors, we are parents with children diagnosed with Microcephaly. Thank you for your interest in making a donation. Every penny helps!

3

Foundation for Children with Microcephaly - Donate - Little Help... BIG Difference

http://www.microcephaly.org/mission.html

Disclaimer: The information provided on this website is to inform and help new parents cope with the sudden, unexpected change in their life. The. Information contained on this site is not intended to replace information you have received from doctors or other health professionals. Though there are. Many facts on this website, there are also many opinions. We are not doctors, we are parents with children diagnosed with Microcephaly.

4

Foundation for Children with Microcephaly - Our Children's Websites

http://www.microcephaly.org/websites.html

A New Kind of Perfect - Emily. Presley and Parkers Blog. Mitchell Stout (You Tube video). Links to Other Great Websites. Microcephaly Support Group (in the UK). Do you have a website for your child diagnosed with Microcephaly, Lissencephaly or. Disclaimer: The information provided on this website is to inform and help new parents cope with the sudden, unexpected change in their life. The. Websites for Our Children.

5

Foundation for Children with Microcephaly - Coping

http://www.microcephaly.org/coping.html

Disclaimer: The information provided on this website is to inform and help new parents cope with the sudden, unexpected change in their life. The. Information contained on this site is not intended to replace information you have received from doctors or other health professionals. Though there are. Many facts on this website, there are also many opinions. We are not doctors, we are parents with children diagnosed with Microcephaly. Doctors cannot tell you your child's future, all they can do is make a.

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For Maddie's Sake, Inc. - Maddie's Blog

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Always give them the chance to try. When they finally do it on their own, stop doing it for them. Sign up for dance reminders. Or was she ever broken? 8203;My mom read this story On Radical Acceptance (& not fixing your kid). It seems to me this is the way to be in this world. 8th grade dinner, dance.then what? I can't believe I'll be in high school next year. I'm the luckiest girl ever, though, my favorite middle school teacher is going with me. I love Mrs. Fussell. She is the best. The dance was a huge...

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Who we are - For Maddie's Sake, Inc.

http://www.formaddiessake.com/who-we-are.html

Always give them the chance to try. When they finally do it on their own, stop doing it for them. Sign up for dance reminders. The best part is making friends along the way! Founded by Richard and Donna Dixon, For Maddie's Sake, Inc. is a non-profit organization (not a tax-deductible entity) formed with the help of the Arc of Texas. And a 10-person board of directors. On July 12, 2010. We hold two free dances per year called Saturday Social Inclusion Dances. Awareness events and causes we participate in:.

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A journey through our daughter's experience with microcephaly and hypotonia. Photos of our Pretty Princess. Http:/ www.westonaprice.org. Http:/ www.helpyourbabywalk.com/mainsite. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out.

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microcephaly.org

Microcephaly - Foundation for Children with Microcephaly

Welcome to the Foundation for Children with Microcephaly! We have created this website. To help and inform parents and families of children who have been diagnosed with. Microcephaly, Lissencephaly, Polymicrogyria and other closely related neurological. If your child has just been diagnosed, you have a million questions and thoughts running. Through your head. It gets really frustrating when no one has the answers to any of your. Questions. We are here to help! Contact a parent now. Just try to help our ...

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