A lot of blogs do a little segment called Thank You Thursday so I thought I’d try it out, especially as today is a particularly poignant anniversary for me.

On May 27, 1995, Christopher Reeve was paralyzed as the result of a riding accident and he became a ventilator-dependent quadriplegic. Reeve used his money and fame to start the Reeve Foundation, which is dedicated to “curing spinal cord injury by funding innovative research, and improving the quality of life for people living with paralysis through grants, information and advocacy.” I don’t know a lot about Christopher Reeve, except that he played Superman and that after his accident, he became the face of spinal cord injury. He showed the world that even if you were a quadriplegic, you still had a brain, you still had a heart, you were still a person and you could still change the world. From what I can tell, his foundation blew the field of spinal cord research wide open and was one of the most vocal proponents of stem cell research (along with Michael J. Fox) during the Bush years.

If Christopher Reeve hadn’t been injured, I am not sure I would be here today. When I became a quadriplegic, my doctors loaded me up with steroids for months. Eventually, the lesions and swelling on my brain stem came down and with the help of the best therapists ever and an unbelievably huge amount of work, I started to get almost all of my mobility back. I don’t know if those therapies were available before the Reeve Foundation started funding research, but I do know Christopher Reeve created an atmosphere of hope for people with spinal cord injuries and paralysis.

I was given the steroid regimen because even though my case looked dismal and there was almost no chance I would regain any mobility whatsoever, it was worth a shot. I was sent to the best spinal cord rehabilitation unit in the state, and possibly the Midwest, because my doctors and insurance company understood how crucial the best physical and occupational therapy was rather than send me to a “long-term care facility”, otherwise known as a nursing home. Even if I had never moved a muscle again, these were the people would try to coax any life out of my damaged nervous system and teach me how to live as a person with a disability. My therapists never gave up on me and I did regain most of my mobility and begin to learn how to care for myself again.

The likelihood is that had I been sent to this particular spinal cord rehabilitation unit (at Froedtert Hospital in Milwaukee, WI), I would have had this experience no matter what. However, had there not been Christopher Reeve and the Reeve Foundation, I am not sure I would have received the same drug regimens at the first hospital or even been sent to Froedtert for specialized spinal cord rehabilitation. Without Christopher Reeve or the Reeve Foundation proving that people living with quadriplegia can still live full and productive lives, I’m not sure anyone would have had any hope for me at all.

##

  • Share/Bookmark

Sunday was the anniversary of a really good day. A great day, in fact. It was the fifth anniversary of the day I was admitted to Froedtert Hospital in Milwaukee, Wis., where I where I stayed for the next two months. I’m sure most people wouldn’t commemorate the anniversary of the day they entered a hospital for two months, but April 11, 2005, was a day that changed my life.

The story really begins five weeks early, on March 2, 2005, when I was admitted to another hospital, also in Wisconsin. (I’ll call this hospital “Hospital X” for the simple fact that I don’t wish to give them free advertising on my blog, for various reasons.) I had been sent to Hospital X from my home in northern Wisconsin because I was having headaches and the doctors suspected my shunt was malfunctioning. (I have Dandy Walker syndrome and hydrocephalus, which produce excess cerebrospinal fluid, aka CSF, in the brain. If the CSF isn’t drained with a shunt, it puts pressure on the brain and bad things can happen. Including death.)

It’s a long story, but while I was at Hospital X, I had a lot of other days that changed my life. On March 5, 2005, I went into respiratory arrest (“coded”). I was intubated, put on a ventilator and transferred to the ICU. On March 6, 2005, I was extubated, after which I promptly coded again. That was fun. During this time, the paralysis settled in and by March 8, 2005, I was paralyzed from the neck down, including my vocal cords. In other words, I became a quadriplegic. I couldn’t speak and communicated by mouthing words and using letter boards. (More on this in a future post.) I spent most of my time at Hospital X in the ICU and experienced many oh-so-fun things like cardiomyopathy, pneumonia, blood clots, a subdural hematoma and countless procedures.

I was really, really, really sick and for a while, they didn’t expect me to live. But of course, I did. In early April, I was well enough to be transferred from the ICU to the regular neurology floor as the social workers and case workers made plans to transfer me to rehab. At that point, I had been in the hospital for over a month. I just wanted to go home. The reality hadn’t set in yet that I was a ventilator-dependent quadriplegic who needed total, and I do mean total, care. And bless me, I thought I could go home to my mom’s house, where she could take care of me 24-7, because moms are super-human, right? Yeah, right.

So it was that on April 11, 2005, I was transferred from Hospital X to the Spinal Cord Injury Center at Froedtert Hospital in Milwaukee, where I spent a week in the acute care. The doctors did their own tests and determined that I had probably had either a brain stem stroke or a spinal cord infarct at the C4 level. After a week, I moved to the rehab side of the unit, where I stayed until I went home on June 9, 2005.

Being in rehab at Froedtert was one of the best things that ever happened to me. (It was unbelievably hard, stressful and exhausting, but still one of the best experiences I’ve ever had.) When I got there, the doctors expected me to be a quadriplegic for life. My physical therapist didn’t care. He decided he would make the most out of whatever time he had to work with me and little by little, just got me moving. By the time I left, I was walking about fifty feet with a walker. I had gotten a lot of mobility in my left hand and arm, thanks to my occupational therapist. The right hand and arm would come back later. My speech therapist rocked so I was even talking again, although I couldn’t swallow well enough to eat. That would happen later, too.

I left Froedtert on June 9, 2005. That was a good day, too. Hard, but good.

I wanted to write this post because I have spent the past month and a half in a state of remembrance. I’ve wanted to talk and blog about my experiences but it’s hard when I haven’t explained the back story. I plan to refer to this post in the coming days, weeks and months so I hope you come back and keep reading. Thanks!

##

  • Share/Bookmark