My daughter, Little Miss Adorable, has Prader-Willi Syndrome. If you are a parent of a child with Prader-Willi Syndrome, let’s connect through the comments on this blog or Twitter @specialneedmom2.
Prader-Willi Syndrome might seem scary at first, most unknown things are.
But, with time, extra support, and a rich life with people who love them, your child will be a star.
More posts about Prader-Willi Syndrome or Little Miss Adorable:
‘etre,’ to be – or if if it ain’t broken, don’t fix it thoughts on Growth Hormone Therapy (rGH) and PWS
Information about Prader-Willi Syndrome on the web:
Prader-Willi Syndrome Association USA http://www.pwsausa.org/
Foundation for Prader-Willi Syndrome Research (USA) http://www.fpwr.org/prader-willi-syndrome-research
Foundation for Prader-Willi Syndrome Research (Canada) http://www.fpwr.ca/
Please add comments about Prader-Willi Syndrome and how it’s touched your life or links to other sites about PWS. Thank you.
©Angela halfpastnormal (2012) All work in this blog is my own and subject to Canada’s copyright laws. If you wish to copy all or a part of any of my posts or blog (including re-blogging, posting links to my blog on sites I do not authorize, etc…) please contact me via email first: