Hello readers, today’s article comes from a face painting mom who has reached out to the community to help her and her son. Kelly Mules posted on our facebook wall about her son and despite sharing it on facebook, I wanted to help them and spread the word more. If you have the time, please find it in your heart to help this brave boy.
The following is from Kelly:

Life was good but all that changed in the blink of an eye, Sept. 2010, when my son got a rare disorder called Guillain-Barre-Syndome. He went form being a healthy, active 10 year old boy in the 6^th grade to being totally paralyzed fighting for his life unable to even breath on his own in just 12 short hours. We spent months in the hospital. Everything in my life stopped and changed that day and nothing is as it was.

The things I loved most like my Faces Gone Wild, faces painting business, artwork and hiking in the Great Smoky Mountains stopped that day. I wanted to trade places with my son, but that wasn’t an option I was given, so I did what any parent would do for their sick child. I became my sons full time nurse, caregiver, therapist, school teacher, friend and mom over night.
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It has been almost 3 years since my son was diagnosed with GBS. He has gotten stronger and his spirit is so amazing and full of life. He is my hero and there is nothing I wouldn’t do for him. I have got my face painting business back up to speed as much as I can and we are learning how to enjoy life and all it has to offer a all new way…in a wheelchair. I have now made it my life quest to make sure my son enjoys life to it’s fullest by introducing him to adaptive sports and looking for creative ways for him to still enjoy the things he loves.
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Transportation is becoming our biggest issue right now. My son is a growing 14 year old boy and I have been lifting him myself in and out of our van for the past 3 years now. He is getting heavier and almost taller then me now. It is really getting hard on both of us. Sometimes I fall over on his lap or set him down in as awkward position and we just laugh…making the best of things. I have put off looking for a handicap van because not only can we not afford but I was truly hoping my son would be walking again by now. The reality is… it’s time to see if we can somehow find a way to get the handicap van we need so we can keep enjoying the things we love.

I have set up this fundraiser for Kyle below so that if anyone would like to help it is an easy way to give, but please don’t feel obligated. If you can’t help right now that’s ok. If you could please share this link with others or just pray with us about this growing need we now have.

[button type=”button_solid_dark nocufon” url=”http://www.gofundme.com/kylemules” target=”on” ]Donate to Kyle Here[/button]