Wash up Post Treatment

Upon waking, the very next morning after receiving the "Virus still detected" result. I Set straight about the business of getting to grips with my situation & my options ! Usually there would be the walk to the kitchen, kettle on & so on. Not today, I reached out & grabbed the laptop, sat up crossed legged on the bed & flipped it open.

"Hmm, right let's think", suddenly Pongos "Hepc trust" came to mind, typed in the name & hit the link. Then spent some time just reading, sent them an email, with a brief outline of my circumstances & carried on reading. All of a sudden I began to realise I'd missed a vital part of any patients treatment or even diagnosis, process, "Information."

How foolish I began to feel, after the lessons learned, through looking after mother, researching our human rights, the patients charter & many other things, now when it came to my own plight I'd sat back & left it to the clinic.
Thinking well all there is to do is give my bloods, do the tests & take my med's, after that what will be will be, Right ! Wrong, within ten minuets of reading I discovered people were being offered extended treatment (tx). That in turn made me think about all that bother about going back to do another blood test at the clinic, after tx had been completed. A reply came in from the hep c trust," Sorry to read of your news, I'm in all morning if you would like to talk", Catherine Corr.

 I rang them up & asked to speak to the person who'd replied. We chatted for some time, if ever anyone needed an understanding ear, now was the time. They Gave me a load of positives that boosted me even more, how my liver had at least had a rest, that there were new drugs on the way. The outpouring, the release was the greatest help & for that I will always be grateful.

Before I knew it nearly two hours had passed, still sat up in bed, my feet had yet to touch the floor. without realising it my come back had already begun. Time for a coffee.

On my way to the kitchen I woke up Jnr & told him how it had played out at the clinic yesterday, followed by my new insight into hep c tx & the new drugs & all the positives that your liver gets from completing tx. He never really let on how he felt about tx failing but he's like his dad, maybe even stronger. After making some what was by now lunch, I decided on a walk, it was another beautiful June afternoon, just what the Dr ordered.

Walking along the road, nearing the bridle path where I turn off into the forest, I noticed a person getting ready for a walk stood by an estate car, they opened the back to let out a labouradoodle, as I got alongside the pair, a voice called out " Peter," I turned to see my old pharmacist, she'd coloured her hair & looked quite different.

This lady was a saint, One of the nicest people I have ever met. Like my Dr she had seen me through most of the 10 years spent looking after mother & Jnr, I'd ask her about mothers med's. One time she even researched new dressings that used a honey from Newzealand & printed out a fact sheet for me. I'd met her parents. We were very good friends as much as a customer could be, but it was the way she cared, for instance if the dr had made a mistake in a script & I had to go all the way back, not only would she stay open for me, but she'd ring up the surgery & tell the staff that she would stay open for me, whilst asking them why it was taking them so long to see to me. This made me fell ten feet tall & gave my dignity a much needed boost.

We walked & talked, she had left the chemist & now worked nearby, we had kept in touch through the old girl who still worked there & so we passed messages through her. So it was, that I knew her sister had passed away some months earlier. As we talked we began to unload our emotional baggage, She remarked that she found this year harder than last when she'd lost her sibling, "that's because you were on auto pilot" I said, I knew all about that, after all it was barely 18 months since mother had passed. I'd been on auto for 10 years. We stopped & talked comforting each other.

I called the trust again a couple of weeks later & spoke to the same lady & told her of the events that afternoon, she like me had drawn the same conclusion, that we had been sent, each other, our meeting was no accident.

 The clinics blood test request had also become clearer. They were thinking of offering me extended tx but why they didn't give me a bigger clue, I'll never know. Tough, when all is said & done I refused point blank their request to go back, so what can you do, shit happens. I made a lot of fuss during tx at times I had cause but my mental state during tx didn't help, I hope they understand that.

Everything happens for a reason , so it is that I sit here now, 16 months on from that still detected result & the afternoon walk with my old chemist. Only now I have redone tx, (12 months this time). I was virus undetected at 8-12 weeks & remained so all the way to tx end. That was 2 months ago ( I kept a diary of my months on Treatment on twitter).

All I can say right now is this time I covered every base, armed myself to the teeth with as much information clinical, medical, practical, spiritual, natural & sensible. Also picking up tips from people like me, who have shared their journey & advice learned. Learned in the best way possible, by "Experience."

This blog has been written because I'm still in the best place to share, as I could still fail. I have noticed The difference between the cleared & failed so my hope is that my words will be taken in the spirit offered. It's also written to keep me busy. Trust me there are some good tips in here, I learned from my mistakes last time. Come the final result I say, Win, Lose or draw, I can look in the mirror & say to myself, "Well kid, you did all you could." As results go they don't get to look much better than this at this point, the virus has been banished, through my own work & effort. The big question is where has it been banished to, some dark decaying corner of my liver or totally routed, April 2011 will be D-Day.

Never say never, my failure plan is to take 5yrs out & live life, then take a look at what's available, what I can say is "there's still some fight in the old dog yet" !


Peace.

1 comment:

ianquill said...

nice one mate and i'll keep everything crossed for April!
Just starting to think about putting myself up for treatment, it's just about a year since my transplant so here goes.
Good luck to you mate and here's to SVR!
Ian