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Welcome to our Family Stories!
Several of our members have prepared family stories. These stories are updated periodically with new (or updated) information.
As you may know, Noonan Syndrome has very many possible symptoms which when you first
read about them can sound quite formidable. But it is a condition with very widely ranging
symptoms, and very few people are affected by all of them. Although there are some whose
lives are quite severely affected, there are also many whose symptoms are quite mild, and
others who were not diagnosed until they were adults and were totally unaware that they
even had it.
We hope you will enjoy reading these introductions, finding out a little about some of
the members of this group, and perhaps even learning a little more about Noonan Syndrome
at the same time.
In addition, many of us have given permission to be contacted for those that want to learn more about Noonan Syndrome, or just need someone to talk to.
If you would like your introduction to be included on this site, or have any comments on how it can be improved, then please contact firstname.lastname@example.org.
Blatchley, Chuck and Sherry
Colodner, Joel and Barrie, Alexandra
Downey, Martha Kate
Jones, Trisha and Kirt
Lance, Daniel MD
Minns, Joy and Jeff
Robinson, Wanda (founder)
Tiren, Craig and Cynthia
Zeh, Art and Linda
The Noonan Syndrome Support Group, Inc. and any associated parties will not be held responsible for any actions readers take based on their interpretation of published or disseminated material. Please review medical treatment and decisions with your physician.