This page is no longer accepting donations
$500
goal
$540
Raised so far

108 % to goal

NEUROFIBROMATOSIS INC

Great Steps for NF 2011 Parkville,  Missouri
Training buddies: Mama, Daddy, Family & Friends

Donations as of May 24, 2013:

$0.00 Raised Offline
$540.00 Raised Online
$540.00 Total Raised

Marching for M'Kenna

Thank you for visiting my fundraising page!

Donating through this website is simple, fast and totally secure. It is also the most efficient way to support my fundraising efforts.

Many thanks for your support -- and don't forget to forward this to anyone who you think might want to donate too!

 

My name is M’Kenna Walburn Heins. I am almost 5 years old and I was born with Neurofibromatosis 1 (NF1). My mom was concerned because I had brown spots that kept growing on my body. Some of them looked like what most people call birth marks. My parents took me to the dermatologist at Children’s Mercy Hospital and the doctor told them that the bigger ones are called café-au-lait spots and the smaller ones under my arms are called freckling which is two of the signs of having NF.

In April 2008 I had an accident while playing with my cousin and the doctor thought I broke my left leg. After being in a cast for six weeks the x-ray showed that my tibia was still bowed. We went to the pediatric orthopedic doctor at Children’s Mercy and she told my mom I had tibia bowing in my left leg which is another sign of NF.

My parents took me to the genetics doctor at Children’s Mercy. I was diagnosed with NF November 2008. My parents have never heard of NF before I was diagnosed.

Most people have never heard of NF even though it is a condition that affects 1 in 3,000 births. Neurofibromatosis (NF) is a genetic disorder of the nervous system which causes tumors to form on the covering of the nerves anywhere in the body at any time. NF can cause cancer, hearing loss, learning disabilities, epilepsy, bone deformities, vision impairment chronic pain and even death. Currently there is no cure or effective treatment for NF. For more information go to www.ctf.org.

You see it is important to raise awareness and raise funds for research to help find a cure for me and others like me who live with NF. So please join us at Great Steps for NF June 11, 2011 to make our walk successful.

Please help and donate online or you can also help by sending your check and in the memo please write my name and participant #308 (M'Kenna Walburn Heins - 308) and mail to:

NF, Inc.

P.O. Box 66884

Chicago, IL 60666

Your donations are very much appreciated and they do make a difference!

Thank you for visiting my fundraising page!

Donating through this website is simple, fast and totally secure. It is also the most efficient way to support my fundraising efforts.

Many thanks for your support -- and don't forget to forward this to anyone who you think might want to donate too!

M’Kenna Walburn Heins

Supporters

Comment Donation
The Knope's
$50.00
Amanda Logsdon
$25.00
Teeter
$10.00
Tony, Courtney and Dylan Lambert xoxo
$30.00
Daddy I love you baby girl!!!!
$40.00
Miranda Miller Have a good walk!
$50.00
Joy Morgan I love you M'Kenna!
$25.00
Brian & Frannie Walburn We love you...keep smiling!
$100.00
Nannie I love you my little lamb.
$125.00
Brian Nehls & Kathy Stipek Have fun on your walk
$25.00
Uncle Bobby Have fun at your walk.
$10.00
Pops & Charlene Pops and Charlene love you M'Kenna
$25.00
Cope Family We love you M'Kenna
$25.00

Donation Summary

Raised Offline
$0
Raised Online
$540
Total Raised
$540
Report offensive content