Prader-Willi Welcome

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.

Little Miss Adorable in NICU

But, with time, extra support, and a rich life with people who love them, your child will be a star.

Little Miss Adorable Dancing

May is Prader-Willi Syndrome Awareness month.

For more Prader-Willi Syndrome articles in this blog please visit my About Prader-Willi Syndrome page.

Also, please check out these excellent Prader-Willi Syndrome resources:

Prader-Willi Syndrome Association USA (my favourite)

Foundation for Prader-Willi Research

Foundation for Prader-Willi Research Canada


About Angela

Super-powered, Special Ed teacher and special needs mama to FOUR (!) children with an assortment of special needs; including Duchenne Muscular Dystrophy and Prader Willi Syndrome. Our family features a heavy dose of good ol' ADHD). I blog about our halfpastnormal life.
This entry was posted in Prader-Willi Syndrome and tagged , , , . Bookmark the permalink.

Like it? Share it! Please comment - I'd love to know what you think.

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Google+ photo

You are commenting using your Google+ account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )


Connecting to %s