Hey my name is molly and i am 17 years old i was diagose with chiari malformation if i spelled that right i am struggling and very new i just found out about this and i am scared and mad about it and it makes me angry all the time because its rare and i have rare blood type anyways which my blood type is o blood and i hjust hate it but please help me figure out what i can do..

Hi again Molly. If you're reading this, then you found your way!

First let me say I just love your name. Molly is the name of one of my most favourite people in the world, and one I love so very much. Molly is my late mother's sister, and she's extremely important to me.

Second..... I'd like to welcome you to NeuroTalk. I'm so sorry to read that you're going through all of this at your age. I'm sure there's times when it's ever so scary, and times when it just doesn't seem fair, but please know that all of us have been where you are right now. Probably all for different reasons, and probably all at different ages, but illness tends to give us all a bond of some sort. It draws us together in search of answers and support. I hope you get both here.

I'm not sure if you've found the Chiari Forum yet, but here's the link just in case. : http://neurotalk.psychcentral.com/forum71.html

Hi Molly! Welcome to NeuroTalk. Have a look around and join in anywhere you feel comfortable. Very glad to have you here!

Hi Molly, and welcome to NeuroTalk! You have found a great place with loads of forums and many friendly and helpful people.

Thank you guys so much ..
i just hate what i hear through some of other people recovery and everything and i dunno but thank you totally and i like this site yall are very nice and very welcoming and thanks again ..