Tough lunch time run, very windy on the trails today.
Tuesday, October 30, 2012
Saturday, October 27, 2012
Halloween Half Marathon, Clayton Ohio
Friday, October 26, 2012
Running the Halloween Half Marathon Neurofibromatosis
Entering Ohio on a rainy afternoon. |
Neurofibromatosis (NF) is a progressive genetic disorder of the nervous system. It causes tumors to grow on nerve tissue anywhere in the body and at any time, which often times result in terrible disfigurement, deformity, deafness, blindness, brain tumors, cancer and death. Some tumors may be surgically removed, but they can grow back. Neurofibromatosis is the most common neurological genetic disorder caused by a single gene. Severity of Neurofibromatosis varies greatly. In families where more than one person has NF, the physical signs and complications will vary for each person. Neurofibromatosis can affect people of all races and genders equally and symptoms vary from person to person. Neurofibromatosis can occur in ANY family.
I always ran alone, thinking about myself and my goals, then I met a group of runners and began running with them. On the average, I was 10 years older than most of them but they gave me the encouragement that I needed to run my first half marathon. When I crossed the half marathon finish line I knew at that point I could do it. I could run a half marathon and even better, I had the confidence to run a full marathon. So in 2011 I ran my first Chicago Marathon. I dedicated eighteen weeks to training for the marathon and my wife was always cheering me on. She believed in me, supported me and made sure that I always had everything I needed.
The morning of the 2011 Chicago Marathon all I could feel was runner’s adrenaline; that feeling of excitement and anxiousness for the race to start. I felt good and I started strong. My pace remained around 9 minute miles, until I hit mile twenty-two and I started struggling. My pace slowed to about 10 minute miles and I just kept thinking, finish, make it to the finish line and when I did I remembered the training, the commitment, and the support and I didn’t expect the struggle. I felt for a brief moment last year after running the Chicago Marathon that this was my last and I wasn’t going to run another marathon but somehow like thousands of other marathon runners that all changed. In retrospect, that last hour of struggling to finish the Chicago Marathon is pale in comparison to those who are struggling with Neurofibromatosis on a daily basis.
Every morning, I wake up thinking how fortunate I am to be able to run. What would I do if I couldn’t run anymore? I think about those who can’t run. I decided I would do it again. I would run the Chicago Marathon but this time, I wanted to do if for different reasons I wanted to do it for those that would never experience the thrill of crossing that finish line feeling that great sense of achievement. I have found there is much more to running than just miles. I am just one man who loves to run and I could make a difference and that difference is to help those that are less fortunate.
I’ve decided to dedicate my running to raising awareness for Neurofibromatosis. Neurofibromatosis does not have a big name spokesperson or a big budget. I could raise money for NF, and I could raise awareness, which in turn, would open new doors and make it easier for those that come after me to raise money for NF. It seems that people are more willing to donate or even listen to your story when it is for something they have heard of. In fact, there are about 2 ½ million survivors of breast cancer and over 2 million people who have NF, it’s that common. It’s my opportunity to make a difference in the lives of those that struggle with Neurofibromatosis. So step by step, mile by mile I am running to raise awareness of Neurofibromatosis.
A year ago I never even heard of Neurofibromatosis, since that time I have learned a great deal about NF as well as how John’s struggles with this genetic disorder. Since deciding to help raise awareness for NF I learned of two more people I know that struggle with NF and then I met another person at a Health expo. So when you hear about Neurofibromatosis chances are someone you know has NF and if you are like me, you didn’t even know it.
Packet Pickup with Sheri |
Pasta Dinner at Tony's at Englewood, OH |
Tuesday, October 23, 2012
Danada County Trails, Herrick Lake
Lunch time run on the Danada Country Trails. Very tough run, the longest run since the Chicago Marathon. It has been over 7 months since I have done the lunch time runs on the trails. Nice break from work! Last long run before my next half marathon in Clayton Ohio on Saturday, number 10 of 12 for 2012.
Saturday, October 20, 2012
Country Lane Trail
Angelica, Maria, Carm, Joanna and I at Country Lane. A beautiful morning for a leisurely run on the trails.
Wednesday, October 17, 2012
Oak Lawn Neighborhood
I tried to get a run in before the rain, ended up getting rained on for the middle 3 miles. Running 5 still seems like a struggle, I guess I have not fully recovered from the marathon.
Monday, October 15, 2012
Friday, October 12, 2012
Oak Lawn Neighborhood
Solo run around the neighborhood. Somewhat of a tough run, my legs are still fatigued. I going to take two days off and hit the trails on Monday.
Wednesday, October 10, 2012
Oak Lawn Neighborhood
Solo recovery run around the neighborhood. I thought my legs forgave me after the marathon. They only said "Really? Seriously?"
Monday, October 8, 2012
Bank of America Chicago Marathon
Perfect weather for the marathon. Came out too fast, first two miles were just under 8 and last two miles were in the 9's, but beat my best time by 16 minutes!
Saturday, October 6, 2012
EVERY DONATION NO MATTER HOW BIG OR HOW SMALL WILL MAKE A DIFFERENCE
On Sunday, October 7, 2012, I will join 45,000 runners in the Chicago Marathon. I am dedicating my run to support, educate and find hope for Neurofibromatosis. I am hoping you will join me in making a difference in the lives of those who struggle with Neurofibromatosis (NF) through a contribution to NF Midwest. Neurofibromatosis does not have a big name spokesperson or a big budget. In fact, there are about 2.5 million survivors of breast cancer and over 2 million people who have NF.
I became aware of Neurofibromatosis, when I learned that a former student in my 7th grade religion class, named John is struggling with the genetic disorder. I never realized he had Neurofibromatosis, in fact; I didn’t even know what Neurofibromatosis was.
John is 22 years old and has had Neurofibromatosis (NF) since birth. He was expected to be blind and deaf by the age of 18. His sight and hearing aren’t the best, but he still has function of both. NF also causes learning disabilities, but that did not stop John from completing high school and completing HVAC training, over a 9 month span. John has numerous cafĂ© au lait (birthmark looking spots) all over his body, along with multiple tumors that affect his daily life and functionality. He is currently seeing a doctor for a tumor on his spine, which causes him immense pain on a daily basis.
Neurofibromatosis (NF) is a progressive genetic disorder of the nervous system. It causes tumors to grow on nerve tissue anywhere in the body and at any time. It often results in terrible disfigurement, deformity, deafness, blindness, brain tumors, cancer and death. Some tumors may be surgically removed, but they can grow back. Neurofibromatosis can affect people of all races and genders equally and symptoms vary from person to person. Neurofibromatosis can occur in ANY family.
Last year, before the marathon, I could feel the runner’s adrenaline; that feeling of excitement and anxiousness for the race to start. I felt good and started strong. When I hit mile twenty-two I started struggling. My pace slowed and I just kept thinking, finish, make it to the finish. In retrospect, that last hour of struggling is pale in comparison to those who are struggling with Neurofibromatosis on a daily basis. Shortly after making the decision to Run4NF, the Oak Lawn Patch did a story on John and me. In the interview John said “I didn’t know that anyone cared about me.” So please join me in letting John and the other 2 million people who struggle everyday with Neurofibromatosis that we care. Together, we have the opportunity to make a difference in their lives.
Click on the links to the right for more information and the link to support NF. If you prefer to send a check, mail to: (Please put M. Blaha in the memo section of the check)
NF Midwest
473 Dunham Road, Suite 3
St. Charles, IL 60174
With your help, the money I raise will create awareness, improve treatments and promote research to find a cure for Neurofibromatosis. Thank you for your support!
With heartfelt thanks,
Michael & Annamarie Blaha
Oak Lawn Neighborhood
Andy and I on our last run before the marathon. Good test for clothing, 7:00AM, 34 degrees, long sleeve Nike compression shirt, long sleeve Brooks dry fit shirt, singlet, gloves, shorts and throw away hat. I am ready!!
Wednesday, October 3, 2012
Tuesday, October 2, 2012
Subscribe to:
Posts (Atom)