Links to stories in the media that talk about Noonan syndrome  News...

Below are links to stories in the media that mention

The Noonan Syndrome Support Group, Inc.

Please note the following stories may have information in them that are not TRUE or consistent with what we have learned most recently about Noonan syndrome. 

Send us an email if you have information that can be added to this page.  Noonan syndrome in the news


The Noonan Connection Fall 2006 (adobe pdf)

 


members AND MEDICAL ADVISORS from the Noonan syndrome support group, inc.

HAVE BEEN INVITED TO attend a conference hosted

by

'Stichting Noonan Syndroom'

Dr. Amy Roberts talk in  Dutch & English

 

 


March 2003

Internet news

I am 20 years old . I was a prem. baby


September 22, 1997

Print News

Wanda

First published Monday, September 22, 1997 Woman unites experts, parents with interest in rare medical disorder


Print News

Raising Alyssa

Faith drives family as child with Noonan Syndrome grows



 

Wanda Robinson,
The Noonan Syndrome Support Group, Inc.,
P.O. Box 145
Upperco, MD  21155, USA
1-888-686-2224 within the USA
or 410-374-5245
info@noonansyndrome.org


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* The Noonan Syndrome Support Group, Inc. is a 501 (c)(3) tax exempt, non-profit organization.
Contributions are tax-deductible to the extent allowed by law.