Questions to the HepC Community (Hepatitis C / Liver Transplant & Biopsy (Hep C) HCV Blog)

Monday, 11 April 2011

Hi all, still waiting to start tx (treatment) as my HepC nurse and Consultant have had holidays- one straight after the other...bloody frustrating as I want to get cracking.

I have been told that as a (HCV) geno 1a, post (liver) transplant, I only stand a 30% chance of clearing the virus but hey, it’s worth a shot – it might get rid of it or at least knock it back until some new drugs come along – I think it’s gonna be another couple of years before transplant patients get Teleprevir / Boceprevir (new HepC drugs) on the NHS in the UK and I can’t wait that long – Still hanging in there folks!
(Pictured - 'injecting Interferon')

They also said that there is a chance that the HepC treatment drugs, being fairly bloody powerful, could react badly with my immunosuppressant drugs and that I could end up rejecting my new liver - eeek. I suppose if my docs have put me forward tx then they must think its worthwhile...?

Just wondered if any of you within the HepC community had any info on 'pre-dosing' with Ribavarin for a couple of weeks prior to commencing with Interferon?

I have heard of a few people who have done this (geno 1a's like myself) and said it was very successful, especially as they had been non-responders 1st time around and had tried this on their 2nd attempt and WON, any info would be greatly appreciated as been told I am to start tx any time soon .

This is the 1st attempt for me even though HCV took my first liver (my liver was too damaged by the time I was diagnosed with HepC) so anything to improve my chances 'post-transplant' would be good.

I realise also that the jury’s out on this issue as it seems that the people who have 'pre-dosed', highly recommend this action and those that didn’t tend to say ‘stick to yr doctors orders’ – I have to say that I haven’t come across anyone who has 'pre-dosed' and then not achieved the hallowed 'SVR' (Sustained Virological Response - or cured to you and me). If anyone does feel that it’s so contentious an issue that they would rather email me rather than post a comment, then I understand – whether they are for, or against it, I’m trying to get info to make an informed choice.

I also wanted to ask you folks about Anti-Depressants, I was reading an article on HepatitisC NewDrugs  (http://goo.gl/fb/v51BG) saying that patients who start treatment from the outset on anti-depressants are far more likely to complete tx than those who don’t. And I wondered if anyone felt they needed pain-killers at any point – I get a lot of abdominal pain but wonder if that’s just because I had a transplant.

Other than that folks all is good and I’m waiting to get on with it, my Hep C Special Nurse rang me to say she has no problem treating me but I have to see the Consultant who got back to work last Friday, once he’s gets to his admin I’ll get an appointment and we should be getting going! Keep everything crossed for me.

Take care everyone… Ian

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Tackling Hepatitis C: A Tale of Two Countries (Hepatitis C / Liver Transplant & Biopsy (Hep C) HCV Blog)

Friday, 8 April 2011

I found this article on the Hepatitis C Trust website and was originally published in The Lancet. As a a Hep C sufferer living in England, it backs up what I have known for some time, having been admitted to my local Hospital twice with symptoms of the virus and misdiagnosed and released thereafter, only for it to be picked up on a blood test done by my GP who didn't accept the hospitals findings. I think this country is in denial of the condition and with 250,000 people suspected of carrying this virus in Britain undetected, it is a disaster waiting to happen!

Hepatitis C remains underdiagnosed and undertreated in parts of the UK. Kelly Morris asks whether the National Liver Strategy for England will deliver what Scotland is already achieving.

20 years after the hepatitis C virus was identified, mortality and hospitalisations are steeply rising in the UK as people infected 20—30 years ago develop end-stage liver disease and hepatocellular carcinoma. At least 250 000 people in the UK might have the infection, mostly undiagnosed, and more likely to present with advanced disease.

Graham Foster, professor of hepatology at Queen Mary's University, London, UK, has “no doubt that more people are being diagnosed with an increase in awareness and testing, but still we are way behind Europe and the rest of the developed world in diagnosing patients and our flow through from diagnosis to treatment is still woefully inadequate”. Foster, who also works as a clinician in east London, tells The Lancet that “treatment services in general are very poor throughout the UK”; he fears that excellent treatment performance and high standards of care are found in few services.

Injection drug use is the main, but not sole risk factor, for contracting hepatitis C, hence the infection is stigmatised and misunderstood in the general population. Prevalence among people who inject drugs is about 50%, yet local provision of testing and treatment varies widely in this often marginalised and unheard of group, despite clear evidence of its usefulness to reduce disease burden and ongoing transmission.

Moreover, treatment and testing are inextricably linked. “If you have a good treatment service, then GPs [general practitioners] become aware that their patients are being cured and that drives them to find the virus and refer patients on”, Foster explains. “If treatment is available at a very low level, GPs stop referring patients because they see nothing happens.” But if specialist services are poorly resourced, then consultants have to place severe restrictions on who gets treatment, he says.

These disparities are increasingly seen now at country level, because action to tackle the virus has widely differed especially between the UK countries Scotland and England, which have similar high prevalence epidemics compared with other countries in the UK and much of the developed world.

England launched a national hepatitis C strategy in 2002 and then an action plan in 2004. This plan, say critics, had few outcome measures, no clear timetable, no attached financing, and the political environment, which focused on priority setting at local National Health Service (NHS) level, was such that the government would not stipulate what was required of local clinical services. “There were absolutely no levers whatsoever to have this actioned. The result is that largely it hasn't been”, says Charles Gore, chief executive officer of the Hepatitis C Trust, which has been campaigning for 10 years for England to develop an actionable plan.

Scotland launched its two-phase action plan in 2006. The 3-year first phase was completed early so that progress and outcomes of the second phase (2008—11) have now been reported for 2 years. From 2007 to 2009, Scotland had a 34% increase in new diagnoses, and a further increase is expected as a consequence of professional and public awareness campaigns, which began early in 2010. Testing has also been enhanced by the roll out of dried blood-spot collection by finger prick, which allows sampling in non-clinical settings.

Development of clinical services has doubled the number of patients started on treatment in 2007—09, while treatment of prison inmates has increased six times. Provision of clean injecting equipment has increased several times since guidelines were approved in 2009. This year, the governance structure and data-generating initiatives now in place will further monitor progress and outcomes. In April, the plan will become part of the Sexual Health and Blood-Borne Virus Framework.

The Scotland Hepatitis C Action Plan “is regarded globally as a model of good practice”, says Gore, who is also president of the World Hepatitis Alliance. To make progress in England, Foster says, Scotland's example “shows how a government-supported initiative can produce enormous dividends in numbers diagnosed and numbers treated”. Gore concurs: “what we in England need to learn is to have outcome measures as a key part of a strategy, to put some money towards it, and to have a clear timetable.” Scotland's total investment in the action plan is about £43 million.

England's action now depends on the forthcoming National Liver Strategy, which is currently in development by the Department of Health and the national clinical director for liver services, Martin Lombard of the Royal Liverpool University Hospital NHS Trust, Liverpool, UK. Lombard has spent the past 12 months working with government policy officials, patient and professional groups, the National Institute for Health and Clinical Excellence, and industry “to develop an understanding of how to tackle the escalating burden of liver disease in England”. Through the strategy, expected in autumn, “we want to transform outcomes for people with liver disease and the various underlying conditions that lead to liver disease”, he says.

Provision of clean injecting equipment has increased in Scotland over the past 2 years

Government commitment to tackling liver disease, including hepatitis, is clear by inclusion of chronic liver disease in outcome frameworks for the NHS and public health, says Lombard, and the National Liver Strategy must link in with the government's vision for the NHS and for public health, published in the white papers Liberating the NHS and Healthy Lives, Healthy People. “Across liver disease, there are significant numbers of patients who need help in their lifestyles to achieve optimum benefit from such a programme. This is an area where we need to do more work with key partners and different agencies”, he says.

“The temptation is going to be to focus very much on alcohol with obesity next as big headline problems”, Gore tells The Lancet. He would like hepatitis C to be the primary focus of strategy: “Out of the main causes of liver disease—alcohol, obesity, and viral hepatitis—hepatitis C is the one bit that is actually solvable in a reasonable amount of time. We could all but eradicate hepatitis C in England within the next 30 years, and make a huge dent in the prevalence in a reasonably short time, if there are clear directions to local NHS on how to go about it in a way that is easy to action.”

Alcohol and obesity must be part of the National Liver Strategy, Foster comments, “but the half million or so people with viral hepatitis deserve a very significant place. There are very large numbers of people infected, the disease burden in terms of cancer and transplantation is huge, and it's a tractable problem where we have solutions”. Conversely, he says, reducing problem drinking requires strategies that are more social than medical, to tackle marketing and availability of alcohol.

Broadly speaking, there is consensus on hepatitis C, “that we need to identify patients earlier”, says Lombard. “Key to this is the need to engage with and up-skill primary and community care services to help us to do this. We also need to do more work with those areas and populations identified as having a higher prevalence of hepatitis C such as drug treatment units, prisons, and within some ethnic groups…many more patients could be treated and prevented from progressing to advanced liver disease if we can achieve this”, he tells The Lancet.

With a new NHS structure and government looking for savings across the board, Gore wonders what will be the levers and incentives to increase testing and treatment. Without safeguards, he says, GP consortia might fail to prioritise or even reduce testing and commissioning of the expensive recommended treatments, with concomitant effects on specialist care. England already ranks second lowest of 14 comparable countries in use of drug treatments, while about a third of patients referred to hospitals in 2009 were not offered treatment, according to the 2010 audit report from the All-Party Parliamentary Hepatology Group and the Hepatitis C Trust.

Amid this uncertainty, the clinical outlook for patients is about to change radically, with the launch of new drugs boceprevir and telaprevir expected within 1 year. When added to existing treatments, these drugs can increase response rates from 40% to 70% in patients with genotype 1 virus and greatly reduce treatment times. “This will transform the picture, both for those who have failed to respond to previous treatment and for naive patients”, says Foster, but could “expose some terrible holes in our service provision”, he warns.

Lombard acknowledges that “some patients who have not responded to treatment programmes in the past may benefit from the availability of newer treatments in the future”. However, he urges, “we need to understand better, and explain better, which particular patients will benefit and what services are needed to treat them”, especially given future financial pressures, and the need to optimise efficiency in services.

Globally, Gore describes the increasing awareness of viral hepatitis B and C infection, as raised last year in a World Health Assembly resolution. July 28 will be the first annual WHO-supported World Hepatitis Day, and WHO is currently drafting a global viral hepatitis strategy. In January, the US Institute of Medicine released a report that recommends steps to improve awareness, recognition, and surveillance, plus integration of care services, to tackle hepatitis B and C in the USA. Foster comments that, “the message from Scotland is absolutely clear. If you set clear targets and you nominate individuals with clear tasks, action happens. If you set rather vague, pious wishes, nothing effective will take place.”

Source: http://www.thelancet.com/ via http://www.hepctrust.org.uk/

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Now The Fighting Really Begins...(Hepatitis C / Liver Transplant & Biopsy (Hep C) HCV Blog)

Friday, 25 March 2011

Okay, so let me tell ya what's been happening of late. I guess it's about time I did as I haven't exactly been a chatterbox recently have I? So I suppose it's about time I put pen to paper so to speak. Truth is, I seem to find it a lot harder to write these days. I don't concentrate as well as I used to and I never was that hot at it even before all this happened - even on my school reports it used to say 'easily distracted, could do better' etc etc. And I find communicating in general a lot more difficult, anyway I'm drifting off the point (and that's something else that was frequently written on my school report!) so let me tell you about whats been going on, 'HepC wise', since I last posted.

A couple of weeks ago, out of the blue, I got a call from one of my doctors at St Jimmy's saying following a discussion by the panel(?); I had been approved to be put forward for Hepatitis C treatment!

Wow, where did that come from? It's true that last month, following my biopsy, that I had asked to be considered for the treatment, but had been told that it would not be considered yet as my doctors were "still trying to protect the graft", it being only a year since my liver transplant and all. They also said that there is a chance that the HepC treatment drugs, being fairly bloody powerful, could react badly with my immunosuppressant drugs and that I could end up rejecting my new liver!

They have been 'messing around' with my immunosuppressant drugs a bit recently, changing me from Neoral Cyclosporin to Rappamune Sirolimus. Not that it worked; my mouth suddenly became a hot bed of ulcers and burned constantly. My tongue swelled up and I was unable to taste anything and inside my mouth became sore and highly sensitive. After a few days I emailed my doc and he rang me back to tell me to stop taking it, revert back to Cyclosporin and that the mouth ulcers were a common side effect of that particular drug. I spent the next week and a half in bed feeling very weak and fevered, waiting for the Sirolimus to work its way out my system. As my doc said, "immunosuppressant drugs are extremely powerful and Sirolimus has a very long 'half life' and it will take time to get rid of it". Great! Looking on the bright side I did lose three-quarters of a stone.  However, my doc told me that if I could stand taking it without getting the side effects, the it was the immunosuppressant drug of choice for post liver transplant HepC patients - Clearly, I couldn't stand it!

They had tried the change of drugs as I had been complaining about headaches, especially if I had been pushing or over- exerting myself or I had just gotten over tired and as anybody with HepC knows, fatigue is a major factor of the virus.

Now when I say headaches I mean bloody bad awful headaches, that would leave me locked in a darkened room for two or three days at a time, unable to stand light, loud noise, barely eat and could just about keep myself hydrated by drinking water only. I had been changed from Tacrolimus originally because of these migraine type headaches and they certainly seemed to be less frequent on Cyclosporin but I still got them nevertheless. It looks like for now though, I'm just gonna have to put up with them. It reminds me of the Tommy Cooper joke "Doctor, it hurts when I lift up my arm like this, so the Doctor said 'Don't lift up your arm then'!"
So after emerging from my bedroom with mouth ulcers and headaches in abeyance, I get the phone call from my Doc saying they are putting me forward for HepC treatment, which is good news, even though I face this news with trepidation.

Why trepidation? Well, treatment for HepC is hard work. For a geno 1(a) such as myself (the hardest of all hepatitis C genotypes to get rid of) treatment is generally 48 weeks and can be as long as 72 weeks. The side effects can be bloody awful (I'll post details about it here next post). But probably the hardest of all is that there is no guarantee that it will be successful; at best 50/50 chance of clearing it and following a Liver Transplant, chance of success is down to about 30%.

Not great odds I'm sure you'd agree but what the hell! The thing is, because of the immunosuppressant drugs I take, the HepC virus has a free hand at knackering my new liver so I guess doing everything I can to get rid of it is in my best interest. And if I can't get rid of it, at least I'm gonna give it a good kick in the balls!

My other thought is this, I can feel how the virus is creeping back into my life, day by day, week by week. I can't tell you how much it has affected me as a person. Going back to Tommy Cooper, he used to use a line "I'm a shadow of my former self", talking about how he'd been dieting. The audience would howl with laughter as there was no obvious change to the way he looked and he would stand there with his characteristic 'hapless' look with just the hint of a smile on his face. I feel as though that joke applies very much to me now. Outwardly, it would be difficult to spot that there is anything wrong with me but I am not the confident, 'glass half full' kind of bloke I once was and for me, this is harder to come to terms with than the side effects of any of the drugs I take now or that I face. Above all else, I feel that this change in my being, like the the virus itself, is killing me and that the odds of beating it are low and the challenge ahead is insurmountable. One thing is for sure - now the fighting really begins!

take care everyone... Ian

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Stripped Bare by George Monbiot via The Gaurdian

Tuesday, 15 February 2011

Hi to all, this is an article written by George Monbiot and published today in The Guardian newspaper - both of whom I have enormous respect for!

Stripped Bare

Shocking new financial manouevres by the British government show who it’s really working for.

By George Monbiot, published in the Guardian 15th February 2011

You think you’ve seen the worst of it; you haven’t. Last week I wrote about how the British government, while imposing extra taxes and devastating cuts on ordinary mortals, has quietly engineered a new tax exemption for the banks and corporations, which also encourages these businesses to shift some of their operations overseas(1). I thought that was as bad as it got. I was wrong.

On the day I wrote that column, the Conservatives were doing something just as repulsive, and far more dangerous. On Wednesday George Osborne told the House of Commons that “we will make sure we learn every lesson that needs to be learnt – so that this [the financial crisis] never happens again”(2). Two days before, his government demonstrated that nothing has been learnt at all. Let me first explain the context.

Most people obtain shares or bonds or other securities in the hope that their value will rise. Short-sellers hope that their price will fall. They might borrow, for example, 10,000 shares and sell them for £1 a piece. Then they pray that the value collapses. If they’re in luck, and the share price halves, they can buy the same number as they sold, for 50p each. They return the shares to the broker who lent them, and pocket £5000 (minus fees).

It’s a controversial practice. Some people say that it helps markets find the right price for their wares. Others maintain that it exacerbates risk, as the sellers are using assets they don’t possess to take on potentially unlimited liabilities (while share prices can’t fall below zero, there is no fixed limit to their increase in value). Short-selling also creates an incentive to try to drive down the price of securities, amplifying or even creating economic crises. An example was the Asian financial crisis of 1997, triggered by a coordinated attack by short-sellers on the Thai baht(3). It destituted tens of millions.

You don’t like the idea? Then take a look at naked short-selling. In this case the sellers not only don’t own the assets they’re selling; they haven’t even borrowed them. They sell a promise of shares, hope the price falls, then try to obtain the shares they’ve sold. In the surreal traditions of modern finance they’re effectively selling securities that don’t yet exist (perhaps they should be called insecurities). Naked shorting may grant short-sellers golden opportunities to wreck companies and economies, by flooding the market with low-cost ghosts.

Almost everyone condemns naked (also known as uncovered) short-selling and wants it banned because of the tremendous risks it presents to the economy. It has already been prohibited in the United States, Japan, Hong Kong, Australia and Brazil(4,5): none of which are renowned for draconian regulation. The European parliament has drafted a directive to bring it to an end within the EU(6). I did say almost everyone, didn’t I? There’s one group frantically seeking to protect naked shorting and strangle the directive: the UK Treasury and Conservative MEPs acting on its instructions.

At a committee meeting in the European parliament last week, the Tory MEP Syed Kamall inveighed against the ban(7). When I asked him how he justified this position, he claimed that ending naked short-selling “will reduce liquidity, meaning that borrowers will insist on higher returns, pushing up the cost of borrowing. This will lead to governments spending more money on servicing debt and less on state-provided public services.”(8) This, as far as I can determine, is rubbish: perhaps the polar opposite of the truth.

Kamall’s office told me his position “reflects that within the government”(9). The Treasury confirmed this: “the UK does not support permanent restrictions on the uncovered short sales of either equities or sovereign debt … we believe it will do much to impair liquidity”(10). Tory MEPs will be instructed by the whips to oppose the ban when they vote on February 28th. The UK Treasury will then oppose it in the European Council.

So here we have a government which claims to have learnt the lessons of the financial crisis, opposing an obvious precaution against insanely risky speculation. How is this possible, when it knows what lax regulation does?

To understand its position, you must first understand that the government is not managing the economy for the people of this nation. It is managing it for a tiny transnational elite, a kind of global gated community. To the people inside the gates, who fund the Conservative party, who own our politics, the media and the banks, the rest of us are an inconvenience, to be bribed, threatened or fooled.

The politicians who get to the top in these circumstances don’t just present no threat to the gated community; they actively do its bidding. That is why Blair succeeded where his Labour predecessors failed. Talent, hard work and intelligence all help, but only if they are harnessed to the interests of economic power.

Governments don’t ask themselves “what can we do that is good for the people?” They ask themselves “how do we persuade people that what we want to do is good for them?” The task of both politicians and the corporate press is to convince us that what is good for billionaires is good for everyone but billionaires. This was the thrust of George Osborne’s statement to the Commons last week(11).

The social isolation of those now in power makes the task easier: they were born into the gated (or moated) economy, and they share its views. Theirs is a different challenge: to disguise their indifference towards the other 99%. They must kiss the babies of the electorate, listen to its complaints, drink its tea – and carry a handkerchief in which to spit. Their interests are not our interests. Their interests are the opposite of ours. If a measure enhances the wealth of the people inside the gates – even if only fleetingly – the government will back it, though it might beggar everyone else. The Treasury’s support of naked short-selling is the homage it pays to naked greed.

An economic war is being fought here. Wealth is being transferred from the poor and middle to the rich at stupefying speed and on a stupefying scale. The financial sector seeks to wring every drop from the productive economy, heedless of the eventual impacts. The government is there to help.

So what do we do? Look to Cairo. I suspect that UK Uncut – the most coherent response so far to the economic transfer – could be the beginning of something very big: a mass citizens’ revolt against institutional theft. The point is not to overthrow the government: that must be done electorally in the UK. The point is to make it impossible to keep fleecing the nation to serve the elite. We go unarmed into this battle; but it’s the government that’s naked.

http://www.monbiot.com/

References:

1. http://www.monbiot.com/2011/02/07/a-corporate-coup-detat/

2. George Osborne, 9th February 2011. Statement on banking by the Chancellor of the Exchequer. http://www.hm-treasury.gov.uk/press_16_11.htm

3. See Joseph Stiglitz, 2002. Globalization and its Discontents. Allen Lane, London.

4. http://www.ft.com/cms/s/0/d2add296-666f-11df-aeb1-00144feab49a.html#axzz1DxOT3Lue

5. http://online.wsj.com/article/SB122518367230175569.html

6. European Commission, 15th September 2010. Proposal for a
Regulation Of The European Parliament And Of The Council on Short Selling and certain aspects of Credit Default Swaps.
http://ec.europa.eu/internal_market/securities/docs/short_selling/20100915_proposal_en.pdf

7. See http://www.europarl.europa.eu/wps-europarl-internet/frd/vod/player?eventCode=20110207-1500-COMMITTEE-ECON&language=en&byLeftMenu=researchcommittee&category=COMMITTEE&format=wmv#anchor1

8. Syed Kamall’s office, pers comm, 14th February 2011. The full email is as follows:

“George – just spoke Syed he is about board a plane now he gave me some new lines for you on the phone,
“If naked short selling of bonds is banned this will reduce liquidity meaning that borrowers will insist on higher returns pushing up the cost of borrowing. This will lead to governments spending more money on servicing debt and less on state-provided public services.”

“A ban on uncovered CDS will mean that investors in infrastructure and other projects, especially in Central & Eastern Europe, will not be able to “insure” their investments by proxy hedging meaning that some projects may not go ahead or they will have to invent new financial instruments to cover their investments that could be less transparent”.”

9. Syed Kamall’s office, pers comm, 14th February 2011.

10. HM Treasury, pers comm, 14th February 2011. The full statement is as follows:

“The UK does not support permanent restrictions on the uncovered short sales of either equities or sovereign debt. No persuasive evidence has been provided to support proposing such restrictions – in terms of either settlement failure or market disorder caused by naked short selling – and we believe it will do much to impair liquidity and increase financing costs for issuers.”

11. George Osborne, 9th February 2011, as above.

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Time goes by so slowly...(Hepatitis C / Liver Transplant & Biopsy (Hep C) HCV Blog)

Monday, 31 January 2011

Well... It just aint been happening for me at the moment folks, which is damn frustrating!


If you haven't already picked it up via twitter or facebook, I didn't get to have my biopsy but just a rather expensive and annoyingly frustrating kind of a week.

As I said on my vid, I was due to go in on Tuesday - Fantastic. So I got up on Tuesday, pumped up and ready to go, dashed around a bit because on that morning I had an interview with a recruitment agency. That went well and as soon as I came out I thought, seeing as I was in town I would do a little retail therapy and hit the shops. I wanted to get myself a wireless internet 'dongle' so that I could keep in touch with the world whilst I was in hospital.

Many of you who have spent time in Hospital will know what I'm talking about when I say I feel so cut-off when I go in to these places, especially for something which you feel is routine or seemingly straight forward and then suddenly turns into a marathon 'staycation'.

If also like me, you use St Jimmy's specialist liver unit, you'll know there are no TV's on the wards. Now I know the phone signal is patchy inside the Hospital but, being a Vodafone customer, I have found that generally speaking I can get a signal. So I headed straight for the Vodafone store and re-emerged 20 minutes later with said item and £20 quid lighter, excellent. Now all I needed was to find was a 'vanilla slice', a cappuccino to go and my retail fix was done, cool!

Ok, once I got home I decided I would put an update on my blog. As my typing is still painfully slow even after all these years of using a keyboard, I decided the quickest way (and as Mandy and the kids were at work and school) was to use Mandy’s' laptop which has a webcam and post a video diary update. (http://youtu.be/vviKROJXEa8)

Ok, so after that I just had to load my 'dongle', pack and soon as we'd had tea and got the kids to bed at 7pm, I would get gone.

The reason for going in the evening before my biopsy was scheduled was to get me into a bed, get some blood taken out of me for tests, put a 'venflon' put in (see image) and then make sure I was 'nil by mouth' from midnight onwards.

Great, so I arrived and everything was going 'swimmingly' until a doctor came round and after 'blowing' a vein in the back of my left hand (not her fault, it's easily done!), we got onto the subject of medications and what drugs I was prescribed. As soon as I told her that I was on Warfarin for a clinical trial, we both realised that having a biopsy was not going to be an option! Goddamit!

I kick myself as I should've realised that taking a drug that thins your blood would probably help you bleed to death when they started trying to 'spike' you to take a peace of your liver away for examination - Warfarin stops your blood from 'clotting'! Ouch! Apparently I should’ve had a letter telling me to stop taking it five days prior to attending. I can only assume that as the study is being carried out by the Imperial College, London and not St James Hospital that it was an oversight and didn’t get sent. This was reaffirmed by the doctor who had no knowledge of my being on the study - bugger.

So after that I was told my bloods would be checked and then could go home in the morning once a new biopsy had been booked. Well, at least I got to check that my dongle worked OK! And I spent the next few hours chatting to guy in the next bed who had recently been 'transplanted' and consequently was still on high doses of meds - he babbled intensely and will probably have no recollection of ever meeting me but I hope I reassured him at the time that he was gonna be OK and was in safe hands. I know his situation only too well!

Next morning I was given a bowl of cornflakes and a cup of insipid tea and informed that my 'bloods' were fine and a date set for the following week to do it all over again! After hanging around to get my venflon taken out, I was released and went down to the main reception. As I'd driven myself in and parked my car in the hospitals' multi storey, I found the pay-parking machine and popped my car parking card in - £15.90!!! Yeas, I'll say that again, 15 bloody ponds, 90! To park overnight for something that didn't happen!!! Bloody Hell, I won't be doing that again.

So after running around the hospital to find a cash-point that worked before the price went up any further, I grabbed a Cappuccino to go to try and get rid of the very bitter taste in my mouth.

So that was last week in a nutshell. I was hoping to get the biopsy out of the way so I could try and make some decisions on moving forward. So many questions at the mo and I can feel the clock ticking away in the background all the while, bloody hell, it's like banging your head against a brick wall sometimes. This damn thing keeps stopping me every time I get started. Ho-Hum, we move on.

I did get some good news; both agencies I had signed on with came back to me with some possibilities of interviews. One fairly well paid but in London (which I'm not opposed to) and one not so but staying here (which is also good). Now I just need biopsy results so I can make a decision on what's best to do!!!

Watch this space, we'll try again this week - I go back in on Tuesday 2nd.

Take care everyone... Ian

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What Is Hepatitis C?

Hepatitis C Information:

Hepatits C is a blood-borne viral disease which can cause liver inflamation, fibrosis, cirrhosis and liver cancer. The Hepatitis C virus (HCV) is spread by blood-to-blood contact with infected person's blood. Many people with HCV infection have no symptoms and are unaware of the need to seek treatment. Hepatitis C infects an estimated 150-200 million people worldwide. It is the leading cause of liver Transplant...

Hepatitis C is an inflamation of the liver caused by infection with the Hepatitis C virus is one of the five known hepatitis viruses: A, B, C, D & E. Hepatitis C was previousley known as non-A non-B hepatitis prior to isolation of the virus in 1989.

Symptoms of Acute Hepatitis C:

Acute Hepatitis C refers to first 6 months after infection with HCV. Remarkably, 60% - 70% of people develop no symptoms during the acute phase. In the minority of patients who experience acute phase symptoms, thet are generally mild and non-specific, and rarely lead to specific diagnoses of Hepatitis C. Symptoms of acute hepatitis C include decreased appetite, fatigue, abdominal pain, jaundice, itching and flu-like symptoms.

Symptoms of Chronic Hepatitis C:

Chronic Hepatitis C is defined as infection with the Hepatitis C virus persisting for more than six months. The course of chronic hepatitis C varies considerably from one person to another. Virtually all people infected with HCV have evidence of inflamation on liver biopsy however, the rate of progression of liver scarring (fibrosis) shows significant inter-individual variability.

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