Support for Sweet Mckenna
$401 raised
22 contributors
5 Years running
Mckenna is a sweet little girl who has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1.

This genetic disease effects every 1 in 6,000 babies. Type I s the most severe form of SMA, and strikes infants between birth and six months old. It is ...
Mckenna is a sweet little girl who has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1.

This genetic disease effects every 1 in 6,000 babies. Type I s the most severe form of SMA, and strikes infants between birth and six months old. It is the number one genetic killer of children under the age of two, and is an often fatal disease that destroys the nerves controlling voluntary muscle movement, which affects crawling, walking, head and neck control, and even swallowing.

Mckenna's mom had to quit her job to be able to care for her, and as you can imagine, medical bills are piling up. There is no cure or treatment for SMA. 90% of babies with SMA Type 1 do not make it to their second birthday. The family should be able to focus every ounce of energy on enjoying their sweet baby girl, and not worrying about how to make ends meet. Please keep them in your prayers, and every little bit helps.

To view her facebook page, go to http://www.facebook.com/groups/358260387575538/

To learn more about SMA, go to
http://www.fsma.org/FSMACommunity/understandingsma/quickfacts/

(This is NOT a scam, and I will be personally sending 100% of the funds directly to Mckenna's mom)
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