This blog covers the history and status of my living with myeloproliferative disease (MPD) and antiphospholipid syndrome (APS) also known as Hughe's Syndrome. My MPD was an unclassified version and possibly combined with myelodysplastic syndrome (MDS) and autoimmune hemolytic anemia. I had a BMT in 2007 and later a bout with Hodgkins Lymphoma but am doing fine today in May 2016.
Thursday, February 09, 2006
Travel and clotting
On July 4th, I flew out to Boston and helped my daughter drive a Honda Civic with two cats back to MN. While we took three days, there were periods when I must have been too stationary, probably during a three-hour stretch through Chicago area in rush hour traffic. The day after I sensed increased shortness of breath. I went in for a CT scan and routine blood test. My Hb was 8.8 and my platelets had increased to a high of 690. Dr prescribed Hydroxyurea, 500mg per day, to reduce the platelets. The CT scan showed another blood clot in my left lung and I was admitted to the U hospital. Clot probably developed in my leg at moved up to the lung. My Hb had dropped to 7.7 after just 2 days on HU so I received another 2 units of blood. While in the hospital for 2 days, I also had an echocardiogram and ultrasound on my abdomen. My spleen, liver, kidneys and gallbladder all checked out OK. A few days later my INR had increased from an average of 3 to 6.7 and we started to measure Factor II, which was 15%. My coumadin prescription was increased twice a week to 7.5 mg per day with 5 mg for other 5 days. Target Factor II is now 20%.
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