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I am watching like a hawk… Thanks for the info.. and I still wish there was a massive campaign about this. Keep the oil coming
Vororo wrote:More on Pamela Anderson… She is cured of hepatitis C, so what is she doing now?
Pamela Anderson Lends Star Power To Fight Against Foie Gras In France!
“In many national cultures, there seems to be at least one cruel tradition that stands out as identifying that culture,” said Anderson. “Be it the bullfight in Spain, eating dogs in Korea, the slaughter of dolphins and whales by Japan or the bloody and obscene massacre of seals in my own native Canada.”
Yeah, right, Pamela. I’m all in favour of animal rights. But what about human livers? There are approximately 4 million in the USA and 750 million world-wide that could easily be saved?
I have thought this too V, and add to that list now cured (via peg/inf) Mr Steve Tyler of Aerosmith, who could help as well. I recall the breaking down of stigma and the support for HIV by stars and royalty alike, and the global awareness of poverty with Geldof’s We are The World, people won Grammy Awards, received Queens honours and so on…these are worthy causes indeed. These are causes that should be incessantly lobbied, yes.
The stats on HCV are still really unknown I think , we only can go by who has been tested, and I don’t like to think about the lack of testing in less developed countries with an unwell GDP and little ability to run on Primary Resources or to develop sustainable infrastructure in Health, Housing and Education. ick:' />
I am sure a projection could be made by a statistician as to the probable number of infected people based on those of us who have been accounted for, and the other data coming into play.Lately many people with public profiles have died as a result of the ongoing fight with HCV. I thought that when Bowie passed away his high profile might have urged some of these rockers to get together and speak up.
I think 2016 we will witness more loss. I hope that these people who have huge social media presence, who have global music markets and the finances to actually break stigma, raise awareness and to assist the global eradication of HCV come to the party.
Thank you for your post, you spoke my language,
ArielThabks Gaj
Yep up the water defs
Gosh my next sx will be growing a hump.
But seriously I just googled and read on a different forum a few had slightly darker urine too at times
I’m almost ready for the 4 week bloods.
If no improvement tomorrow or if it worsens I will pop in to see my GP or even urologist.
All loving non medical and medical assistance greatly appreciated
Splashes
ArielThanks heaps LG
Couldn’t be a bladder infection no, I can’t feel anything like that niggle, and my kidney function was okay the week prior to beginning txI’m drinking so much water I swear I could have filled a small pond by now Day 22
Maybe this darker colour plus the migraine back is dehydration?
I have had a kidney lithotripsy last year so I know it’s not stones that really hurts. I do have two small cysts one 4cm on one kidney and one 1.5 cm in the other since peg/inf just like the stones.Probably just a messy few days
Ariel
Thankyou so much Chejai x
My vision is blurry more than usual yes and sore eyes I think that sun has done this
I read other people’s posts about sun sensitivity
I have never had dark urine. Has a bit.
Wondering if that’s to be expected too can anyone help share some experience please
Thanks all
Splashes,
ArielI kept my riba bottles and made a sculpture of a person, stuck nails into it to join the bottles.
Then I binned it.
I returned the last five weeks of that repulsive stuff when the locum pulled me off peginf riba
I consider the sculpture and my little ceremony as a cleansing of the specialist who never told this lady here anything about fibroscan or gene tested me or sx and at F0 (found that out post tx!!!! By locum) but he did know VL only 422000 started me on a journey to hell all in one day from results of activity to that.
I didn’t know ANYTHING about HepC at all
I was a mum with a daughter in final year of school and one in Uni she’s an International Scholarship recipient.
Now the damage has been done to me I have education
But I was very hurt by what happened
I’m glad I had my little ceremony in private here
It was cathartic in a sort of black weird way.
Day 22 here so not far behind you babe
I look at these bottles and think of them as priceless and they are all about kindness and saving lives and moving forward and getting back some of what was taken from me for no reason at all.
That’s all.
overLove always here Ariel xxxx
Ever felt like this?
You’re in loving company hereP
Thanks Tina
Vale Paul Hester a fantastic funny guy
I’m loving this one xxxxxxxI am at Monash too I can help you sweetie xxx you can use the medicine from here I can explain how to keep the peace and still be able to go to Monash it’s our nearest clinic after all
I have private health insurance too xx we may have sat side by side at last liver clinic not sure but I did talk to a lovely young lady who was anxious
Lots of love Ariel xxxxJosie-Eynaud-facebook wrote:I am 23 and have been diagnosed with hepatitis C three months ago. I am an otherwise healthy girl, but have been very sick from November 2015. I only contracted the virus in May 2015, and was tested positive 7 months later.
My blood test results are: GGT 76, AST 84, ALT 107. I have been experiencing severe nausea, vomiting, and Inappetence for the last 3 months. I am on no medication or vitamins for any health conditions, except that I’ve been using Stemetil or Phenergan for the nausea and vomiting, but to no avail.
I have private health insurance and I am absolutely desperate for help! I am willing to travel around Victoria, Australia for treatment, but not out of Victoria as I get very home sick.
I am on a waiting list at Monash Medical Centre, but I’ve been told that I could be waiting for a couple of months before even having an appointment booked with the gastroenterologist/hepatologist.I’m becoming extremely depressed as I am unable to work and do most daily activities because of the constant nausea and vomiting.
I’ve lost weight and struggle to keep hydrated as I can barely keep anything down.I live in Inverloch, Victoria, and I am asking, pleading for help.
TIA.I live near you
I’m on tx from this site
You are not alone
Private message me if you would like support during this time
I’m a mum and one of my daughters is your age xxx I am a local surfer and ex school teacher
Sending you love xxxxxxxKeep the pressure on NZ
AWESOME work team NZ love your passion
Lobbying is a draining and sometimes most frustrating task. My letter to then PM Tony Abbot was hand delivered via a secret route and his reply indicated he had not read my letter
I disclosed my identity my degrees my interferon debacle my loss of income
I explained the matter of the burden to the health industry and the causal effect it would have in Australia to deny tx
He wrote back the most inane drivel
It was a personal letter not written by a staffer but by himself
It just made the hair on my neck stand up at his complete head in the sand retort.
Same type of reply from two other leaders here.
Lobbying is hard work when $$$$$$$ are involved at this level of greed. Also the scaremongering trying to con people into waiting eternally for the PBS that never came that’s been promised but hmmmm ve vill see!
Go NZ GoLG I see it is a toasty 7 Celsius in London! ARGGGHHHH!
Yes Blue Book LOVE IT
”Lynne-Francis-facebook” wrote:Hi Not sure if this is the right place to be for my question…I have five days to go before I finish treatment. The past week I have felt incredibly down and unhappy….not my usual demeanor……very teary. Very anxious about my post 12 week blood test….not sure if it is maybe being anxious about the result…… Has anyone else experienced this?
As an interferon relapser I was even scared of starting any new tx…I am scared of relapsing…I am scared of sx, I am scared of a lot of stuff BUT I think this is completely normal.
After all, I realise I have not been well for a darned long time, in my case Lynne, I was not told of any sx going into peg/inf, in fact when I asked I was told about people who ‘worked all the way through peg/inf’, and how they ‘breezed’ through it, no no truth was told. I was NOT told about fibroscan and not given one. I am F0! I was urged in fact to commence tx immediately.
I was not gene tested, I was not told about this and when I finally was taken off tx at 43 weeks with heart trouble by a locum while the Gastro person responsible for this failed duty of care was away, I relapsed within four weeks.These and the last four years of rebuilding my completely destroyed body have made me nervous.
I agree with LG, I have decided to praise myself, and that is; focusing on the triumph of reinventing myself, of taking the bit between this old nags teeth and giving this a go…of never giving up hope, and of just accepting baby steps are my thang.
I asked about relapsing going in, via a pm to Dr James, and I know if the worst happened it is not all lost and done and dusted for any of us. I think that this is a great issue you have raised.
We will be okay. After tx a nice cleansing lifestyle to detox these meds too…lots of swimming in the sea (not very close to Bendigo ) massages, walks, new hobbies, trying something we have never done before…these are great things to distract the mind.
I feel your anxiety, and thank you for the honesty Lynne xxx
ArielThanks for the lurve friends,
My eyes this morning are pretty blurry
I must say the best thing is I realised……for ever and ever, as long as I have a memory I have been having tiny ‘blackouts’ when I go surfing…they have definitely gone. (I didn’t know this until now..lightbulb moment)
LG I was playing keys the other day and my clarity is improved too there and that is my wobbly third leg workwise… so that is a good sign too.
Thankyou all for the props it helps me immensely feeling the collective spirit. Thankyou for the advice and recounting of dealing with these medicos and staff who are less than charitable…. I didn’t say this earlier on, but my Public Hosp. specialist made me switch from Mesochem to Indian…
Blue Book has been purchased…well it is aqua. And large.
I just am so pleased to be getting better…well I guess I am haha! Bloods at week four. Day 20 today so tomorrow is my 21st Birthday…YAY let’s eat cake
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