Lee's Latest Post

Chair Pic 05/17/08

As I sit here in Detroit, packing my things and fresh out of the emergency room, I felt it may be a good time to post. For those of you who have no idea what I am talking about, I should probably elaborate.

Following the last post I went into finals and finished up another semester of school. It was a semester that at times seemed pretty rough, but ended up rather well with three A-‘s and a B. I will take that any time, especially with a semester consisting of differential equations, thermodynamics and dynamics.

Early on in the fall semester I had decided to return Detroit this spring. I felt I had made significant progress the first time I was there, and it was worthy of at least one more shot. So when the beginning of January rolled around and all of my classmates were headed back to…well…class, I continued working and increased my workouts to fill my free time. Then the beginning of March I packed my things and headed off for another Michigan adventure.

When I arrived, I found that the person who had been the head of the program when I left had since been replaced. The meeting with the new head was disheartening at best. I was told that therapy would not benefit me and that I would be better off to save my money and return home, but I knew better. Also, that if I did choose to stay I would not be allowed to participate in weight bearing therapy, i.e. walking, crawling, kneeling, or anything else really. So I decided go against his suggestions and stay for a few months, and see what would happen. Now I just needed that bone scan. It seems like a relatively simple concept, go to the doctor and get it done. However, due to conflicts with scheduling and with my insurance company, I had the pleasure of making the 20 hour round trip for the weekend to get it done. It did work out all right, though because it happened to be Easter weekend and my roommate had some of our friends in from out of town.

Once I got back and the doctor got my bone density results there was relatively little headache before I was back in full swing with my therapy. It again consisted of a lot of, coupled with PNF therapies, working on a slide board to improve hip flexer and glute contractions, crawling, tall kneel crawling in a second step, and KAFO walking. I don’t have enough room to get too specific about these things in this particular post, but if you have any questions, let me know. A typical three hour session may consist of any combination of these. I have been walking about 600 feet at a time, tall kneel crawling about 300 feet, and crawling about 150 feet at a time, all of which are improvements of the last time I was here. Also while I was here I have been continuing with my strength training as well as doing a lot of handcycling. I competed in a 25k race in Grand Rapids, MI a week ago. I finished 10th out of 27 cycles with a time of 68 minutes. Considering the fact that it was my first race, and my lack of training compared to many of the other riders, I was pretty happy with my finish. For those of you in the Des Moines area, I am sure you a familiar with the 20k Dam to Dam run. I will be competing in that in two weeks.

Now to address that perplexing opening sentence, my intention had been to stay here one more week before returning home. Therapy has been going well. I had just wanted to be home to enjoy the summer. Well things here got a little hectic. Thursday during therapy I was really not myself. I was incredibly sore and achy and suffering from pretty serious bouts of dysreflexia. That afternoon after returning to my room I found myself fighting a high fever, headache, and all round miserable evening. At that point I was convinced I had contracted another UTI. When I awoke the next morning I found it was something very different. There had been a spot on my back where it hits my seat back which had been slightly discolored for some time, but I had never had any problems with skin breakdown there. However, at some point during the night it had turned into an open wound. I headed over so the therapists could check it out and tell me what they thought. They immediately dismissed it as a pressure issue, because of the massive amount of swelling and obvious infection of the site. The general consensus was go to the ER, so I did. There they diagnosed it as an abscess caused my staph or a similar infection. It was pretty large, about 5 inches long and 3 inches long, right in the center of my spine. So they lanced it drained it, and put me on two different antibiotics. So with combination of the now open wound and the side effects of the antibiotics, I talked to my therapists and decided that if may be time to just return home.

I am planning on driving to Toledo tonight so stay with some friends of mine, then making the long journey home tomorrow. So here I sit, packing my things, fresh out of the emergency room.



This is Me, and this is My Mission, FOREVER IS NOT AN OPTION.



Homepage

My Story

Ok, so here is the deal. If you have found Free Lee you probably know what it is all about. However, if you do not, here is a little information to get you started. My name is Lee Harris. (Thats where the "Lee" comes from). I am a 20 year old mechanical engineering student at Iowa State Univerisity. On Semptember 12, 2005 something happened that changed my life. I was involve in a bad motorcyle accident in which I shattered my spine. I had surgery to put my vertabrae back together with pins and rods but the major outcome of the surgery is that I am completely paralyzed from the chest down and am now confined to a wheelchair. (For those of you who really know your stuff my injury is technically a "T-5 T-6 Asia-A") The doctors give me no chance of recovery. I however have a different fate in mind. After spending 6 weeks in the hospital, and another month or so at home with my parents I now live on my own. I go to school, I work, I party, I drive my own pickup. (If you want more info about me check out my Carepage , my carepage name is HarrisISU, or send me an e-mail. My email address is harrlee@iastate.edu) All of that is great, but my goal is to one day get out of this wheelchair. (Hints the "Free" part). The only way that we can find to do this right now is olfactory stem cell surgery followed by intensive rehab. The surgery is experimental and is therefore not covered by insurance. Although the rehab will be done in Detroit along with all of my preliminary doctors visits, the surgery is only done in Lisbon Portugal. Because of all of these complications I will be forced to come up with over $150,000. That is why I have this site. I am an extremely independent, strong and motivated person, but I can not do this alone. I need as much mental, physical, and financial support as I can possibly get. If you have read this all the way through you must have some interest in my quest and I greatly appreciate it, every message, dollar, and prayer I can get will get me one step closer to my goal.

Thank You,

Lee E Harris

The Fundraising

Fund Meter

This is going to be a very important part of making the surgery possible. If you have any ideas, questions, or concearns let me know. We are currently trying to figure out how to raise the money. Any time we come up with something, I will be sure to put it in the Future Events Section. One idea we do have is my logo, perhaps shirts, stickers, posters maybe with the logo on the. If anyone out there would be interested in purchasing or producing them please contact me. The benifit of something like this is two fold. Not only could it possibly help me raise some money, but it would also be a huge promotional deal and would really help the raising awareness part of my mission.

In addition to these ideas for fundraising, general donations will always be welcome. If you would like to donate, there are a few ways you can do so. The first is to go the fundraisers, and donate there. Another way would be to give the money/check to myself or one of the members of my team, and we will make sure it get processed properly. The final way to donate is dirrectly to the organization that is organizing our funds. The name of the organization is National Transplant Assistance Fund (NTAF). We are having them collect the money because we are trying to avoid the complications of having the money in our name. However, if you go to the site, the infor there can be somewhat confusing, so I will clear some of it up. On the site it says the funds go to a regional fund. Now this is true, but I am the only person that can use the that particual regional fund, so the donations placed into the website will all go to me, and not to any other member of NTAF. The other good thing about this site is that you can donate with cash, credit, or check. This makes it somewhat simpler, and even if you do give them money to myself or my team, we will be placing it in the fund. If you have any questions about any aspect of the fundraising please contact me so I can help.

For aditional information click the fundraising tab at the top of the page or click here.

Future Events

More detailed descriptions of the event can be viewed by clicking on the event. I will update this whenever I find out something new and can remember to post it. Thanks.





Update

Random foliage

I recently ordered 1000 more stickers and they should be here soon. If you want one and still don't have one, or know somebody who wants one let me know. Also, I am still looking for people to send me their pictures of their sticker stuck to things, so if you have any, send them to me. If you don't have any, take some, then send them to me. Once I get them I will post them all in the callery section of this page.

Thanks.

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