Dylan Fitch

Dylan Fitch I am 10 yr old boy. I have Chiari Malformation and seizures. I am the youngest of 5 kids 1 big brother 3 big sisters
PayPal- fitchdylan@yahoo.com

SunTrust bank (Dylan Fitch)
This account was opened for lil Dylan for donations. Any donations would greatly help and go straight to helping him with all of his medical needs. Thanks

In Feb. 2008 Dylan fell and went into a seizure. He was transported to the hospital where they did an MRI. He was then refered to the Neuro Surgeon at Childrens Healthcare of Atlanta. The doctors did some extensive testing and found that he need a Decompression(brain surgery). In Aug. 2011 Dylan had the surgery. He seemed to be doing well after the sugery. After about 2 months he started to show more symptoms of his Chiari. We watched him and talked to the doctors. They decided to run more test and try new medications. None of the medications helped and all of the test showed that he will probably need more surgery. Dylan had a 2nd decompression March 2013. This surgery was more extensive then the 1st. They had to cut the lining of his brain and push the bottom of the cerebellum up and stitch it up. June 2014 Dylan had a seizure and fractured his C-1 (neck). He was in a neck brace until Oct 2014. He is still have some issues with burning sensations in his head and neck. Alittle info on Chiari Malformation ...

What is Chiari Malformation? Chiari malformations (CMs) are structural defects in the cerebellum, the part of the brain that controls balance. When the indented bony space at the lower rear of the skull is smaller than normal, the cerebellum and brainstem can be pushed downward. The resulting pressure on the cerebellum can block the flow of cerebrospinal fluid (the liquid that surrounds and protects the brain and spinal cord) and can cause a range of symptoms including dizziness, muscle weakness, numbness, vision problems, headache, and problems with balance and coordination. There are three primary types of CM. The most common is Type I, which may not cause symptoms and is often found by accident during an examination for another condition. Type II (also called Arnold-Chiari malformation) is usually accompanied by a myelomeningocele-a form of spina bifida that occurs when the spinal canal and backbone do not close before birth, causing the spinal cord to protrude through an opening in the back. This can cause partial or complete paralysis below the spinal opening. Type III is the most serious form of CM, and causes severe neurological defects. Other conditions sometimes associated with CM include hydrocephalus, syringomyelia, and spinal curvature. Is there any treatment? Medications may ease certain symptoms, such as pain. Surgery is the only treatment available to correct functional disturbances or halt the progression of damage to the central nervous system. More than one surgery may be needed to treat the condition. What is the prognosis? Many people with Type I CM are asymptomatic and do not know they have the condition. Many patients with the more severe types of CM and have surgery see a reduction in their symptoms and/or prolonged periods of relative stability, although paralysis is generally permanent.

Dylans having a full Spine MRI to try and see why his legs go numb and why his back hurts
11/13/2016

Dylans having a full Spine MRI to try and see why his legs go numb and why his back hurts

Excellence in Math and AB honor roll
05/19/2016

Excellence in Math and AB honor roll

11/25/2015

Please share this with your friends

07/09/2015

Im going to a bike ride out of town and I get to see some other kids with chiari and show them my truck mommy and daddy has made for me i cant wait

Me n my truck
04/17/2015

Me n my truck

04/08/2015

My daddy has been working on my truck and as promised was finally able to get my steering wheel installed that my good friend David McAughty gave us in October i cant wait to share it with everyone we'll post pictures in a few days thanks mom and dad and david

Today is Rare Disease Day so share this picture in support of all of us
02/28/2015

Today is Rare Disease Day so share this picture in support of all of us

More pictures of Project Dylans Christmas , Thank you to all the businesses and friends who done this . We are truly ble...
12/27/2014

More pictures of Project Dylans Christmas , Thank you to all the businesses and friends who done this . We are truly blessed and great full for your kind hearts . We love each of you for sharing this with Dylan and making him smile

Dylan wanted to Thank everyone who sent him Christmas presents this year . Here are the pictures we captured of him open...
12/27/2014

Dylan wanted to Thank everyone who sent him Christmas presents this year . Here are the pictures we captured of him opening them . We cant thank yall enough. We love you all and are truly blessed to have great friends who do this on there own . Kyle Killey thank you brother for your kind heart and love for Dylan we cant thank you enough.

I had so much fun at the Dropem Wear show yesterday. Thanks to Dave love you man!!!
10/19/2014

I had so much fun at the Dropem Wear show yesterday. Thanks to Dave love you man!!!

10/16/2014

Doctors said my neck looks healed in the xray . But they said it wasn't broken either with an xray so thats why they did the CT and MRI so mom and dad wants another Ct or MRI to make sure . So for safety reasons mom and dad wants me to wear my neck brace until we get these done just in case its still broken i dont hurt myself anymore. Thanks for the prayers and support

My cousin is doing a school report on me and i think its cool she even added dads truck pretty cool thanks alicia love y...
10/15/2014

My cousin is doing a school report on me and i think its cool she even added dads truck pretty cool thanks alicia love you

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2455 Spaugh Industrial Dr
Winston-Salem, NC
27103-6498

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