Not my usual big blog but at least I will keep y'all up to date. I'm sorry my being gone both with blogs as well as love on y'all's sets. Y'all all know from previous posts I'm a game and movie fanatic so that's were all my time has gone. I was addicted to borderlands 2 I'd start playing for a bit then realize it was like 3am haha. Then finally when I wasn't zombie tranced to a game I got really sick. Getting sick for me is always really bad cause of my heart transplant. I have to have a really low immune system so it doesn't hurt the transplanted heart which making some small sickness into a big deal so that took up 2 weeks of my life. Then of course I've seen like every movie released in the past 3 months haha in my next blog I will talk more about that. Lastly the thing that really has stolen my time is halo4 to put it simple it's like crack a little is never enough haha. I would stay up all night playing ify friends stayed up haha.
One more thing if medical stuff interests you. I've gotten a call from the main muscular dysteraphy association in America to be a parient study. I haven't agreed to it cause it worries me but they say if I do it I can really help people understand my type of muscular dystrophy. Mine is a very rare type they have very little on it cause its extremely aggressive when it first starts cause it attacks the heart and most don't survive that I luckily did so that's why it's important. It's odd tho its aggressive at first on the heart it slows down dramatically after. Like most people with muscular dystrophy lose the ability to walk close to there 20s yet I still can not well I might add but I don't need a wheelchair at home. If you have opinions on this matter I'd like to hear them cause I still don't know what I'm going to do.
One more thing if medical stuff interests you. I've gotten a call from the main muscular dysteraphy association in America to be a parient study. I haven't agreed to it cause it worries me but they say if I do it I can really help people understand my type of muscular dystrophy. Mine is a very rare type they have very little on it cause its extremely aggressive when it first starts cause it attacks the heart and most don't survive that I luckily did so that's why it's important. It's odd tho its aggressive at first on the heart it slows down dramatically after. Like most people with muscular dystrophy lose the ability to walk close to there 20s yet I still can not well I might add but I don't need a wheelchair at home. If you have opinions on this matter I'd like to hear them cause I still don't know what I'm going to do.