... some ... loss. ... bad ... Hi my name is Alyson and I'm 41 years old.I was born with congenital heart disease.I had pulmonary stenosis and atrial septal...
HELLO, MY NAME IS DEBRA, I HAVE A SON WITH NOONAN SYNDROME. HE WAS DIAGNOSED AT BIRTH. IF THERE ARE ANY QUESTIONS THAT YOU MIGHT HAVE. I WOULD BE HAPPY TO HELP...
Oh my gosh I have a million and one ? to ask you. How did he get diagnosed at birth? It took me a year and 3 major hospitols.Peyton was just labled delayed and...
hello I am new here an really need help in understanding this for I have an 8 year old who has been diagnoised with noonan syndrome.,she has got the features...
Hello, I see this is a very slow group, but I figured I'd check it out :) My name is Shannon, I have 3 kids, soon to be 4. We are adopting a little boy who...
Hello, My name is Jacqui and I am a mom of a 10 year old boy who has experienced many of the same difficulties (physical, emotional, and educational) as many...
Hi, My name is Beth and my son Zachary was just diagnosed with Noonan Syndrome this past week. He is almost 14 months old. He tested positive for JMML at 2...
Hello, all! I am a special ed teacher and have been researching Noonan's syndrome lately. Didn't realize how rare it was and how little info is out there....
hiya my name is jane, my son jonathan has noonans .. i wouldnt change him for the world he has his own little personallity ..we do have our moment with him tho...
Hi - my name is Heather and I have a daughter Becky (9) with Noonan Syndrome. (There is some information about her at www.hnye.com) Looking forward to...
My Name is Kim and my Son Kyle(16) was born with Noonans. Well that was a dumb statement, of course he was born wit it, you don't catch it. Kyle is pretty...
... heart ... the ... this ... Hi Beth Nice to meet you. I am glad Zach does not have any heart problems. Kyle also had feeding problems. he failed to thrive...
Hi, My 7mth old son Bailey was diagnosed with noonans last week. It's a 2nd shock for us because he was also diagnosed with jmml (juvenile myelomonocytic...
Hi Lorraine, My 14 month old Zachary was diagnosed with noonans in mid-October. He also was diagnosed with JMML in October 2003. The doctors didn't think that...
Hi, My son Ryan 6 years old has Noonan Syndrome. We are going to have our first heart surgery on December 6th. He has Pulmonary Valve Stenosis as well as...
Hi Beth, I've just been reading Zachary's caringbridge page. I logged onto jmml webpage and saw one of your messages. How strange that you should be sending...
HELLO, I RECEIVED YOUR LETTER THROUGH, BEING ON THE NOONAN WEB SITE.I TO HAVE A SON WITH NOONAN SYNDROME/ HEART DEFECT. I WANT TO KNOW MORE ABOUT THIS JMML....
Hi Debra, JMML is juvenile myelomonocytic leukaemia. Children with either noonan's or jmml are more predisposed to getting the other we've been told. If your...
I would like to talk to anyone who has a child with Noonan Syndrome.My son Connor has NS, he is 11 years old and would love to know if anyone out there is...
my baby has noonans, so I cant be of help we just found out for sure last week.does your son have heart defects as well? Kirsten mom to alexandria 12, ethan 2...
I am someone with Noonans the younger years were the worse I still have some problems. which I don't care to talk about and even though I am an adult ...
how do you cope? I mean kids are mean..alot of adults too! I was made fun of and being someone who didnt have any visable problems that was tough. What did...
Hi I had a question for you. Your son is 11 yrs old. When did he get diagnosed with NS? How did he get there? I have an 11 yr old son who our doctors refuse to...
Hi, My son Ryan has NS, he is 6 years old. My son was dx as a baby by a genticist. He has Pulmonary Valve Stenosis, Woffle Parkinson White Syndrome, Hearing...
thats great advice! I was trying not to worry yet as Owen is 7 mos. but its good to know for the future. I have has several adults ask me whats wrong with...
I know your asking someone else but for us, Owen has heart defects, doesnt eat by mouth had lost weight AND he has facial characteristics of a child with...
Hi. My name is Ann and I live in Sweden. My daugther Frida has NS, she is now 2 years and 3 months old. When she was born and up to a year old they said they...
