Monday, November 26, 2018

Our Brave Bailey 
#BaileyCPWarrior 
This is the story of our brave little 4 year old daughter, Bailey, who has cerebral palsy.  Bailey is kind, intelligent, and fiercely independent.  Even though her mobility is limited by a walker, she is determined to do everything that everyone else can do, no matter what.  Bailey dreams of doing all of the fun things that peers her age are doing, such as climbing on the monkey bars, swinging, rolling down a grassy hill, riding a bike, sitting with her legs crossed in front of her, exercising, and most of all…dancing.  This desire has led us to reach out to a neurosurgeon in St. Louis, MO who performs a life- altering surgery called Selective Dorsal Rhizotomy (SDR).  After doing loads of research, and speaking to parents who have had this surgery on their children, we have decided that this may be the best chance for Bailey, to help her combat some of the painful, lifelong impairments caused by this condition.  Dr. Park has predicted that, after this surgery, Bailey should be able to walk independently, across all environments which would be a dream come true!!

 A fighter is born

Bailey was born on May 26, 2014 at 27 weeks gestation, weighing in at 2 lbs. 2.5 oz. and spent 2 months in the NICU.  When Bailey was 1 month old, we were informed that she had developed a bleed in her brain (diagnosed as Periventricular Leukomalacia or PVL).  She continued to grow and develop but was pretty late in meeting some of her milestones (rolling over, scooting, crawling, etc.).  Just after her 1st birthday, she was diagnosed with Spastic Diplegic Cerebral Palsy. 

Bailey-1 day old
First kiss from mama


Bailey-1 month old


















 

Our family-July 2014


 
The Diagnosis
Cerebral Palsy is a neurological condition that permanently affects muscle control and coordination.  Spastic diplegia affects the legs and arms, making them stiff and contracted (spastic), although in Bailey’s case, her legs are much more affected than her arms.  At just past 2, she got her first reverse walker, and has been on the go ever since. 

With CP, comes many challenges, including an endless battle with spasticity (tightness, constant muscle spasms in her legs), making everyday things, such as walking, sitting up independently, or even sleeping very difficult.  Through medications, botox injections, and countless hours of physical therapy, she can now go to preschool and experience the world with the use of her walker.

Bailey's 1st birthday




 Enter Dr. Park—the life-changing operation
I was introduced to the St. Louis Children’s Hospital Selective Dorsal Rhizotomy group through a fellow CP mama on Facebook.  It was through this group that I found a kinship with a ton of parents that are dealing with the same challenges that we have been dealing with, and found a way to try and improve their child’s situation through Selective Dorsal Rhizotomy or SDR.

SDR is a procedure that treats muscle spasticity by cutting the nerve rootlets in the spinal cord that are sending abnormal signals to the muscles.  By reducing the spasticity, the surgery can help improve walking patterns, help with potty training (which in children with CP can take as long as 5-6 yrs), and can help improve range of motion and functional mobility.  The leading neurosurgeon that performs this surgery is Dr. T.S. Park at St. Louis Children’s Hospital.  Dr. Park has performed thousands of these surgeries and has trained many neurosurgeons on his techniques for a less invasive surgery than has been offered in the past.  Although there are risks to such an involved and invasive surgery, the long term benefits that it can provide are definitely worth the journey. 


Here is where you come in…
A major, life-changing surgery like SDR comes with a large price tag.  The overall expected cost of this surgery (and braces/equipment is just over $46,000, which is WAY out of our budget.  We are expecting our insurance to pick up some of this, but since it is out of state, we don’t really know how much they will cover.  This is where we need your help!  As parents, we want to provide our children with as many possibilities and opportunities for success as possible, and this is our way of doing that for Bailey.  We want her to be able to live a life where she doesn’t have to rely on dangerous pharmaceuticals to get through the day, or have to worry about the deterioration of muscles as she gets older, and the pain this deterioration will cause.   

For more information about SDR, please refer to the St. Louis Children’s Hospital website ( http://www.stlouischildrens.org/our-services/center-cerebral-palsy-spasticity/about-selective-dorsal-rhizotomy-sdr), which explains what Dr. T.S. Park does for these amazing kids.31461154_153385442669828_r.jpeg