Friday, July 9, 2010

Day something

Weekend is here and I am fairly excited since it maybe the last weekend I am in the metro Detroit area. I am eating dinner over Mike and Em's House on their new patio. Sunday I am playing my last night of poker in who knows how long. I leave for Kzoo area next week to spend the rest of my days with my lovely fiancé, Kristyn.

As for my health my chemo has been put on hold since my Atc in my liver was too high. I am not sure if it was Atc or something like that but should be fine next week and can get back to schedule. So chemo wise I will start my 2nd round on the 14th. Hope this update helps thanks


Love Scott

Tuesday, July 6, 2010

Days didn't work

I still post as random as ever, and can't keep you updated as much as I would like. Right now I am busy with my personal life. I am moving to Hartford Mi in a couple of weeks. I still have to pack and get my crap together for that. On my health note I get my second round of chemo tomorrow and we will see how I been doing. Nothing really pressing or important. I will let you know if anything happens. Love you all

Scott

Friday, June 25, 2010

Day 3 Post

So as you can see I can't even post everyday it bores me and I know it would bore you to read this. Today was my last day of PT so now I have to work my ass off at home to get my leg straight. It will happen but I need to work on it. Should be a fun weekend and Kristyn is still trying to find us a home. I know we will get one it just takes time. Thats that...Oh played poker till 2am that about killed me....Good night y'all

Wednesday, June 23, 2010

day 2

Today was much easier to type out. Went to PT and found out that it my coverage runs out Friday so I have alot of work to do at home. Which I know I will battle with it. My friend brought me some pizza and watched a tape delay of the US Futbol match which was amazing. Felt like I was there. Then blah blah blah I went to bed. Day 2 in the books

Tuesday, June 22, 2010

day 1 longest of all days day 2 will be better

Day1:

This is very new what I am doing. More everyday posts of what my life is and where it is going. This will be the longest of the Day updates since I have to update you on what has happened since the last post. I have had a trail chemo i think I told you about but what I didn't tell you is that it is making me more nauseous than the other drug but have been fighting it off with some meds.

Thank you all for coming out to the benefit on Thursday June 17th it was a great success due to the Molly Rose McCormick and family on a great great outing. font change I guess. The dinner had a turnout of 220ish and all to support me some how way shape or form. God who knew I had so many peeps that loved and supported me. THanks again for this night. I will remember it for ever.

I have had some stomach issues that me and my mother have had some teamwork on and broke me down a bit but I am looking for the end of the tunnel to just have the easy part of life to live and not this hell of what i call a life. Let me just say I can't walk can't control my bathroom habits and need someone to make sure I get what I need and rides to Pt and other doc appointments. I mean I just want a break from all the shit.

We are looking for a house and that has become a hassle but I am glad Kristyn and Jeanne has taking the reins on that one. I love my friends and family and the really close people know who they are I want you to know all the help and love you send is the best thing I could ask for. I love you all.


Love Scott

Tuesday, June 15, 2010

Long time new update

So its been a really long time since I touched this blog. I have been busy, really busy but that is no excuse not to get you updates. In my life I am planning a wedding, buying a house, doing lots of PT, and starting a Clinical trial. All these things have both Kristyn and I stressed out but we are going to keep on trucking and make this all happen.

Kristyn moves to the west side of the state on Sunday and my mother moves back in to help me with PT. Both my ladies in my life have been great and put up with my inability to walk and me asking them to get me stuff and drive me places all the time.

The clinical trail I started is a Europe drug that has worked on sarcoma cancer. It is a 24hr infusion every 3 weeks. I get 3 infusions then a new CT scan to see if the drug is responsive to my cancer. I am excited to start this trail see if it works and if it doesn't i will move on to the next drug trail what have you.

I am in great spirits right now just excited about all the life changes things that are going on in my life. I am no longer employed and focused on my health. I am making ends meet with help from my parents and others. For those of you that don't know Molly One of the nicest people I know is throwing a charity dinner in 2 days on Thursday. She has worked really hard on this dinner so if you can show up then that would be awesome. Thanks for reading hope all is well in your life.


Love,
Scott

Sunday, May 2, 2010

New news isn't always good news

Weeeeeeeeeeell. As you all know I have battled and kept the positive attitude and still am in the trenches trying to fight off this nasty thing. We had thought that the worst was behind us and that the best was yet to come but I have more to fight before I can state that.

We can start with the good news. My leg bypass was a great success and am recovering great from it. I can get my leg a little straighter and Kristyn, mother, PT lady, and myself are working to get my leg straight. I am hoping that by middle end of may I should be walking with a limp which I can't tell you how much of an accomplishment that will be. Just being able to walk will make me an easier problem for everyone to deal with.

Now on to the news that some know but not all. My tumors have moved to my brain. Yeah I know I don't have much up there to start with but the dear old cancer thing has decided to go upstairs and now I have to deal with that. The way we are going about that is called full brain radiation. I have 14 tumors so this method should kill all the cancer in my brain. I am going to U of M hospital to see what clinical trails I can maybe try to better my chances at this game of life. Sorry it too long to update this but as you can tell I been dealing with some things that are bigger than me. Love you all.


Scott