55 y/o male with hep c dx from 1998 (probable exposure in 1970) . Three biopsies indicate consistent decline (now at grade 3). I have continued to work full time, despite episodes of fatigue and neuropathy in my feet. In the past year the fatigue has worsened significantly and I now have begun experiencing joint pain in my
handsHand or foot spasms
Hand tremor. My G.I. Dr. consistently has not been very proactive in my condition. More than four times, it is I who has requested timely blood work. In May of this year, I had to remind him that it had been over a year since my last viral load. On two subsequent f/u appt's the report was not available and he said he would f/u on next appt. I saw him last week (no mention of the blood work) re: my continued decline and my inability to attend work consistently due to "cycling" into periods of almost debilitating fatigue, now lasting several days at time. I requested to begin treatment and to be placed on disability, to avoid losing my job and benefits; specifically my long term benefits which would pay me 66% of my base salary. He blew me off, telling me "he doesn't do that" and referred me to the Stanford Liver clinic which has a clinic monthly at the local hospital. By the time I'm able to be seen I may have already lost my job from calling in sick to much. Also, how can I be evaluated and ask for a leave of absence from someone who has no history with me. It may come across has a malingerer when my "specialist" has refused to do it. Likewise, if I change doctors it may look as some form of "shopping" in order to get off work. I don"t no what to do. I have a
familyBirth control and family planning
Choosing a primary care provider
Ewing’s sarcoma
Family troubles - resources to care for. This disease is difficult enough, let alone having to be treated in this way. Sorry for the long question, but what should I do? Thankyou
Good luck,
Chiara