Cytarabine or AraC, should I or should I not?
Yesterday I went to Kings College Hospital in London, to get the results of my second Bone Marrow Biopsy, see the Professor and find out which …
I am an educational adviser and agent who specialises in bringing and caring for Russian Students who come to UK for all types of education, boarding schools, pre-university Foundation Programmes, under graduate degrees and post graduate degrees. Married to Judith for the last 22 years, with 6 children from previous marriages. Having has MDS for a year, I am told I have now moved on to Acute Myloid Leukaemia.
I am an educational adviser and agent who specialises in bringing and caring for Russian Students who come to UK for all types of education, boarding schools, pre-university Foundation Programmes, under graduate degrees and post graduate degrees. Married to Judith for the last 22 years, with 6 children from previous marriages. Having has MDS for a year, I am told I have now moved on to Acute Myloid Leukaemia.
Yesterday I went to Kings College Hospital in London, to get the results of my second Bone Marrow Biopsy, see the Professor and find out which …
Thank you and im sorry for your prognosis, i appreciate you mail. Its all happened so quick he was diagnosed on the Tuesday and went to hospital alone at his insistance on the Thursday. he hasnt asked any questions so i have insisted on going to hospital with him for a check up on Thursday this week. Will let you know when I find out anymore.
I'm glad you were able to enjoy the poem, sir, and thanks for your favorable comment sent to me.
Thinking of you and praying for the right choice! I cannot help you with defining the chromosome 8. Best of luck! Angie
Cause I like your accent!
In August 2008 I went into hospital for a vascular operation on my right leg. They took a blood sample and told me my platelet count was down to 66, so I must undergo a bone marrow biopsy, which showed I have MDS. Starting to plan my Funeral Service, but will enough people come to fill the church? Don't fear death, but worry about not being able to live a useful and active life.
I have been diagnosed as having MyeloDyspraisa since September 2008. Today I was told I have crossed the boundary and now have AML. I am given 3 to 6 months to live, and have been offered Chemo/Cytarabine, which gives me a 15 - 20% chance of living longer than the 9 months of the chemotheraphy course. The odds do not seem too well stacked in my favour.