My son Connor was diagnosed at 17 months with NS and it has been a
sparodic mutation (no one in either families have it, it just
happened out of the blue.) I think just as well I didn't know what
was in front of me but deep in my heart I know that god gave me
Connor and Lee for a reason.

Lynda mum to Lee hypothyroidism, episodic ataxia type 2, and
schizoaffective disorder. Connor NS,PVS,Asthma, large liver
spleen,hyperexstensive joints and much more.



--- In noonan_support@yahoogroups.com, "Robyn" <dictatorqueen@...>
wrote:
>
> We're still waiting to find out if we (the parents) have NS or not.
> Our first boy (2.5 years) is fine, our infant (5 mo) was diagnosed
at
> birth.
>
> We're waiting for DNA confirmation as to whether hubby or I have
> passed it on.
>
> Would we have had kids had we known? I'm not sure. Possibly not. It
> definitely would've changed our outlook.
>
>
>
> --- In noonan_support@yahoogroups.com, "heather51308"
> <jamieandheatherscruggs@> wrote:
> >
> > Did anyone here know they had Noonan Syndrom before having
children??
> >
>