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| 2014 IronMan Relay |
Hello and welcome to my Blog, my name is Jaime Salas and I wanted to take a quick moment and basically say who I am and why I am starting this Blog. Well like my beginning sentences says my name is Jaime Salas, I am 40 years old. So why start a Blog at this age and for what reason? Well this Blog is to inspire and maybe help those with have Charcot-Marie-Tooth find a place they can hang out, chat about the disease and get some info all at the same time. Yea, I know it sounds like something someone made up and is trying to make money off of some fictitious disease. Well it's real, its REALLY real. Charcot-Marie-Tooth is a debilitating disease that effects the nerves. The name comes from three different doctors who discovered the disease in 1886. Yea it's that old!
Here is the short short version of how it effects people with Charcot-Marie-Tooth or CMT. CMT basically is a neuropathy heredity disease, passed on from generation to generation. Though it is mostly prominent in males, not to say that girls can't get it, they just have a smaller chance of getting the disease at birth. Though keep in mind CMT can effect people in many different ways. Here is the best way I can explain it: There is a sheath that coats the outside of your nerves called Myelin. The purpose of myelin is to basically help send a signal from your brain to your muscles to fire off. Meaning to move a specific muscle, well this Myelin sheath the coats our nerves is either non existent or is slowing going away as we start to age. So when we ask our leg muscles to lift our leg or point our toes so we can walk properly the response from our muscle is very little or no response from our legs at all. So we do a lot of foot dragging, and tripping over things, as well as having balancing problems, as well as problems with our hands.
Some people think of it as drop foot or or Charcot Foot, they have identical symptoms, but they are two totally different disease. CMT doesn't only effect the legs or the feet, but can effect hands as well. Their are other cases out there that CMT not only effects the extremities, but can start effecting the lungs and other vital organs from what I hear are extreme cases. So in short CMT can be a very crippling disease. If you really want to dive in to the in's and out of CMT click on this web link to get more detailed information.
NIH Charcot-Marie-Tooth
So now that's out of the way, let me explain a little bit more what I plan for this Blog. To me Blogs are not just informative pages, but it is for those people who want to share their experience with other like minded, or with others who are going through the same thing and who can empathize with the writer/blogger.
So my blog is for those of us who are not sitting on our arses and working to keep our selves healthy and mobile. CMT has not slowly started to effect me. One I was young I was super active. I was a soccer player, I used to love to run and basically do everything a young boy/young man loved to do. I never had any real problems with my legs as a young adult. It wasn't until my later years, and I would have to guess in my mid to late 30 that CMT started effecting me. To top things off in my messed up gene pool, my family has a history of Type II Diabetes. Well yes you guess it I was diagnosed with type II diabetes about a year and 3 months ago. So I obviously I had to make a change in my life if I wanted to keep living. So I did! I changed my diet for the diabetes, and then one of my best friends in the whole entire world had introduced me to the world of cycling.
Since that time I have lost close to 50+ pounds and have been living a much healthier life and I owe it all to him and my loving and supporting wife. Cycling has now turned into a passion of mine. To give you a small glimpse of my accolades in a one year period, I have ridden close to over 800 miles in one year. One event that I am super proud of myself, is that I ridden over 103 miles while climbing over 9000 feet of elevation in one of my local mountain areas. I have also completed a Half IronMan Relay where I cycled in the hot Nevada desert over 56 miles with over 4000 feet of climbing in 100+ degree temperatures. So as you can see, cycling has got a good firm hold of me, and I love every bit of it. I have done some swimming and a little walking since I have a bad tendency to drag my feet when I walk fast or try to jog due to CMT.
So I want to make this blog for those who are athletes or recreational swimmers, cyclists, and runners with Charcot-Marie-Tooth and talk about their experience from the first time you decided you are going to make that change in your life, to those who just found out that they have CMT and are wanting some advice, or tips for training. I want this blog to be for everyone who is just wanting someone to chat with about the disease and be with people who understand what it's like to have CMT.
What I am bringing to the table is that in 2016 I will be entering in my first EVER Ironman event. I have started training and I have until July of 2016 to prepare myself mentally and physically for a 2.4 mile swim, a 112 mile of cycling, and a 26.2 mile run. And I want all of you to be with me 100 percent of the way as I train and go through the trials and tribulations of all the mental and physical blocks I will have to over come as I prepare for my first ever Ironman event. I will blog everyday on what I am doing as well as post pictures all the way up to the day of the event.
Most importantly I want to hear from all of you on what your future goal is for 2015 or those long goals like mine in 2016. I'd like to hear what you are doing to train and what you are using for orthotics or other training devices or orthotics that can help others break those physical barriers.
Thanks again and come back and see how well I am progressing or see how I am struggling mentally and physically.
Thanks again for reading my Blog anddon't forget to following me!
-Jaime