My wife has been blogging for years. Something like 10 years. I have been publishing blogs for a long time too, but there isn’t alot to publishing one for someone else. You just put it up and it’s out of your hands. But this will be my first REAL attempt at blogging about something that I feel might be worth falling on potential viewers.

In setting out on this journey, I hope I get to meet new people that have the awesome gift that was given us… mutated red blood cells. Mediterranean disease as it has been called, leaves us with mutated gene structures that limit the oxygen carrying qualities of the red blood cell, leaving us with a shortage of oxygenation to the body. Anyone who breathes knows how important sufficient oxygen is to a healthy body, much less a living one. Turns out there are countless “symptoms” that this asymptomatic disease leaves in its wake.

I hope that this blog serves as a conduit of information that is invaluable in helping those of us with the blood disease that the medical world deems too small to care much about. T-major gets attention as it should, since it leaves its victims with certain death, and a lifetime filled with blood transfusions. T-minor has its share of miseries that make it very hard to cope in a world that doesn’t consider our disease as something more than a nuisance that surfaces in the worst of circumstances.

I will be leaving posts nearly daily if possible. Some posts will be just me talking about whatever it is I feel like talking about, but most will be on topic and will deliver some sort of insight as to what I’m doing to make my body feel as normal as possible as often as possible.

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