Well, I haven't written anything for a while. And It's surely not because I have nothing to write about. Or should I say , Need To Write About! This writing thing is a huge tool in my program. It has helped get all the crap out of my head and make room for the good or Great stuff that absolutely surrounds us everywhere. Its just the way we think about things sometimes that make situations seem to be here to stay.
As it is said "The only constant in life is change". Not going to get to deep into that right now nor anytime. Because you can talk and theorize for hours , perhaps even days and you will always come back to the same thing.."The Only Constant In Life Is Change". I had a sponsor once that attempted to show me... A day of someone alert enough to his surroundings and that takes nothing for granted, had the ability to teach this ole foggy sole a lesson that will be with me till I am no more of this earth. So Yes...We Do Change. Every addict no matter how bad can change!
Now, I have a lil trash to dump. As most of you know I have Cirrhosis of the Liver. Secondary to HCV which was secondary to blood I received in 1979. I lost my right leg below the knee and dam near lost the left one also. I received tons of blood and blood products (over 100 units in a 4 month stay in ICU) Of course in 79 they didn't screen for Hep c because they had no idea what it was. If you died from it or developed symptoms you were labeled Non A B. Anyway my symptoms eventually stopped me in my tracks in Nov. 2013. I was treated with triple therapy. That stuff came very very close to killing me. I went septic so bad I only had a slight chance to live....But they didn't have a clue who they were messing with! lol...so In September 2013 I was chosen to receive the new Hep c drugs. Olysio and Salvaldi. I cleared hep c in 12 weeks of therapy. But my liver was crapping out. That stuff is hard on all your organs.
My old diseased liver continued to De-compensate over the next 3 yrs. Man I was sick as a dog every single day! Now here's the kicker or perhaps the blessing in my situation, With Cirrhosis you get NO pain meds at all. My doc lets me take 2 Tylenol twice a day. ...Now back to what I was bitchin about. I am on the transplant list but due to my lengthy I.V. drug abuse I will only get to the top 5 in the nation. And I shouldn't deserve that. Anyway I got to hurting so miserably I went to my local e.r. The immediately flew me to Vanderbilt in Nashville, where I am on list and have all the workups done. After a couple of days they found that the hepC had returned and my liver was super small and very Nodular. Its not regenerating nor making new cells that live longer than a couple hrs. Looked like I was pretty much tits up this time.
I was started on Ribavirn and Harvoni. This makes me feel worse than ever. And absolute no sleep at night at all. I sleep when I can usually 2 hrs at a time. I am suppose to be on this therapy for 24 weeks instead of the usual 12. they say its due to my liver not metabolizing enough of the drug to help so I need to be on a longer regimen.
Thanks for letting me dump all this...I don't have to many people coming around to see me anymore ...Most if not all friends I have live hundreds of miles away.I left home in 1982 and started a career in Heavy Civil Construction. I made friends at the many many jobs at worked at or supervised. Some still keep in touch but I miss the work and the adventures on the road.
Hope you all stay clean no matter what....Things always change...That Light at the end of the tunnel is an oncoming train no-more!!! See...I told ya.....Cause someone else told me!!
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