Alliance For Cryoglobulinemia
You Are RARE But NOT Alone
About Me
- CryoLady-Cares
- My Maddening Maze began suddenly, when I was just 47, with a plethora of autoimmune diseases. The life I knew changed forever due to chronic debilitating fatigue and pain. Faced with challenges beyond my understanding I began a never ending search for answers. I was later diagnosed in 2010 with a Rare Disease, Cryoglobulinemia Vasculitis. This disease causes my blood to gel in what appears to be temperatures lower than 70 degrees. When this phenomenon happens it can be life threatening causing organ damage, stroke, eye and vision loss along with a host of other complications. Both my kidneys and heart have been attacked by this uninvited guest and each day brings new challenges both physically and mentally. I live to find answers for myself and others that are afflicted with this rare disease and to find joy in living, whatever the cost. My passion and purpose is sharing the voice of the patient lost in the Maze and offering the face of Wellness in spite of it all.
Monday, December 20, 2010
LITTLE KIDS ASK, "WHERE IS HE"? CAN YOU ANSWER.
So many emotions, feelings, travel thorough us especially at this chilling time of year. Do you know what you believe in? How important is it to you or are you just to busy to even worry or think about it. I'm not here to judge, just question. I wish someone would have asked me that questions many years ago so I would have realized how important it is to search for something, someone to believe in. No one has to agree with you. No one has the right to judge you for your discoveries. But life is clearer when we believe.
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Please contact me at mvennitti@allianceforcryo.org if you would like to know more about Cryoglobulinemia Vasculitis.