Find all needed information about Microcephaly Support Australia. Below you can see links where you can find everything you want to know about Microcephaly Support Australia.
https://raisingchildren.net.au/disability/guide-to-disabilities/assessment-diagnosis/microcephaly
Financial support for children with microcephaly If your child has a confirmed diagnosis of microcephaly, your child can get support under the National Disability Insurance Scheme (NDIS) . The NDIS helps you get services and support in your community, and gives you funding for things like early intervention therapies or one-off items like wheelchairs.
https://rarediseases.org/organizations/microcephaly-support-group/
The Microcephaly Support Group (MSG) is an international, voluntary health organization in the United Kingdom dedicated to providing information, support, and networking opportunities to families of children with microcephaly, a condition characterized by abnormal smallness of the head.
http://www.childrenwithmicro.org/
Microcephaly, holding fundraisers or parent-to-parent support. Disclaimer: The information provided on this website is to inform and help new parents cope with the sudden, unexpected change in their life.
http://geneticalliance.org.au/conditions_detail.php?Microcephaly-357
Help Support Genetic Alliance Australia. Click on Bert, the Genetic Alliance Frog - to make a donation. All donations over $2 are tax deductible. ABN 83 594 113 …
https://www.facebook.com/groups/241561679197141/
MICROCEPHALY SUPPORT GROUP has 4,453 members. To support families who are affected by Microcephaly in anyway Wether you are a parent, grandparent or...
https://www.facebook.com/Microcephaly-Australia-251686071568209/
Microcephaly Australia, Nambour, Queensland. 430 likes. This page is for people to share there life journeys, please feel free to share stories.Followers: 449
http://www.geneticalliance.org.au/conditions.php
If you cannot find your condition here, or you would like to add a support group to the list, please contact us directly by phone or email. If you know of a change of contact details for a support group listed here, please contact us so that we can update the website. Please …
https://www.circleofmoms.com/microcephaly-support
Started by Ana Karen on 06/24/2017 in MIcrocephaly Support. Last update on 06/24/2017 by Ana Karen. 1. Holding up head. Hello, I have a 21 month baby with microcephaly, and developmentally is more like a 2 month old baby. I was just wondering if anyone had advice on how I …
https://rarediseases.org/rare-diseases/lissencephaly/
In addition to signs and symptoms of classical lissencephaly, infants with Miller-Dieker syndrome may also malformations including microcephaly with a broad, high forehead; bitemporal hollowing; a relatively wide face; micrognathia; a long, thin upper lip; a short nose with upturned nostrils; low-set, malformed ears; polydactyly; abnormal palmar creases; cataracts and/or malformations of the heart, kidneys …
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