2006 (Kellisa's First 18 Years)

 

2006 started with Kellisa’s 4^th surgery in four months. Both hips were dislocated again, requiring another surgery of cutting bones, inserting screws, and hardware. It was followed with the same six brutal weeks of recovery.

 

After 18 months without a trip or trail, I was eager to get Kellisa back outside. I wanted to push our limits and see what we could do on trails. I even bought the largest baby jog stroller I could find so we wouldn’t have to use her wheelchair anymore. 

 

2005 (Kellisa's First 18 Years)

After a few good hikes in 2004, I thought 2005 would be our year to get out and explore. The outdoors would be ours!

 

I was wrong, very wrong!

 

The year started out with a surgery to remove the hardware from Kellisa hips. The six-week recovery period was as brutal as the original surgery. Thankfully, The Wiggles were there to help Kellisa through another difficult six weeks.

 

2004 (Kellisa's First 18 Years)

I was traveling a lot for work and when I had to spend the week before Memorial Day weekend in Atlanta, I invited Lisa and Kellisa to join me. It was a mini vacation. I could join them for lunch and evening swims after dinner. I started researching hikes with wheelchairs. I found a short accessible trail leading to a viewpoint of the highest waterfalls east of the Mississippi only an hour from Atlanta. Finished with work, we drove to the trail on Saturday morning.  I was bursting with excitement. I found a hike I could do with Kellisa. It was a beautiful trail, and I easily pushed Kellisa to the viewpoint. The waterfall was breathtaking. The endless mountain views were inspiring. Kellisa was having fun. This was Kellisa’s first wheeled hike on an accessible trail. I was disappointed beyond belief.

 

2003 - Part II (Kellisa's First 18 Years)

Kellisa wasn’t drinking and her only fluid intake was through the limited food she was eating. There was only so much pudding we could force into her mouth. She wasn’t thriving and required surgery to place a G-tube in the summer. With a G-tube, we would be able to give Kellisa the fluid she needed, and prescription formula would guarantee she would receive all the nutrition required to start growing. Of course, Kellisa suffered from complications that required a second surgery to remove the original G-tube and replace it with another. The doctor had been placing G-tubes for 26 years and Kellisa was the first patient to ever require a second surgery. Kellisa was an expert at confusing doctors.

 

2003 - Part I (Kellisa's First 18 Years)

 

Kellisa was slowly dying before our eyes and no one in the medical community was able to figure out what was wrong. 

 

Kellisa's smile and love of life were gone. She was battling high fevers for weeks. Nothing was bringing her temperature down to normal. She saw a doctor every few days and was in and out of the ER and hospitals without any relief. Once again, Kellisa was baffling the doctors. 

 

From early on, Lisa was convinced it was the shunt. After a CT scan and MRI, we were assured that the shunt was fine. Kellisa's shunt had been in place for a long enough time that a shunt infection was very unlikely. The neurosurgeon didn’t want to tap the shunt to check the cerebral fluid for an infection because if it wasn’t infected, the procedure itself carried a 2% risk of infecting the shunt.