We Are Not Alone Convention - Early Bird Pricing for Registration

[Guest guest]

To All of Our Special Stars & Their Family's,

The Foundation for Children with Microcephaly has recently celebrated

their 3rd birthday having official 501©(3) nonprofit status. We

want to include our families in our celebration by offering Early Bird

pricing again to register for our annual convention for three days

only!

How it Works:

Download your registration form at www.childrenwithmicro.org/wearenotalone.html

- Send in your completed registration form and payment POSTMARKED ON

MAY 3, 4, or 5th and receive Early Bird pricing to register for our

amazing annual convention. This special pricing can save a family

$100 or more! In order to participate and qualify make sure that your

envelope is POSTMARKED ON MAY 3, 4, or 5th!

Families who register on or after May 14th cannot be guaranteed an

appointment with the world's leading physicians, but can be placed on

a waiting list. There are still physician appointments available -

send in your registration form to secure your child's doctor

appointment!

You too can contribute to making this year's convention bigger and

better! Let your local hospitals, doctors offices, & therapists know

about FCM and our unique annual convention, " We Are Not Alone " . They

may know other children diagnosed with Microcephaly, Lissencephaly,

Polymicrogyria or other closely related neurological disorders. Refer

them to the website so they can let their patients know about our

convention. We want this year's convention to be the biggest and best

- we don't want any of our families to miss it because they didn't

know about it! Thank you for helping us spread the word!

Feel free to call us with any questions or concerns! We still need

help organizing the convention - if you have extra time on your hands

and can contribute please let us know!

Thank you all for your support! I look forward to meeting you at " We

Are Not Alone " - the 3rd Annual Microcephaly Convention! Remember...

we also welcome families who have children diagnosed with

Lissencephaly, Polymicrogyria and other closely related neurological

disorders!

Best Wishes,

Jenni & Kaylee

Jenniffer

Founder/CEO

Foundation for Children with Microcephaly

jenni@...

www.childrenwithmicro.org