Recently I was informed by the NHS that the drug Ferriprox and its treatment are to be limited to 90 days, thereafter they will no longer supply either. Their reasons were that the application had no weight to it though we are also informed that people in other areas are getting this funding. I am getting together a letter to our local MP to see what he thinks as well as to ask whether my medical status is because of a postcode lottery.
Health wise, I am finding I have the shakes more with my entire body and I am much more tired. My second (and last) hernia opperation is set for the 20/2 as long as my blood count is ok.
Late February I was granted a years supply of Feriprox and care.
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