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Being very extatic and happy now!!!!!
Got my blood taken on tuesday – there was a technical problem at the hospital so I couldn’t get it taken friday as planned.But today I got the result!!
In just 3 weeks I beat this !! My testresult is negativ…Of course I have to finish the cure, so I’ll stay on the meds for three months as planned. My doctot said I had to so I will. But she expected this to be a finished chapter for me
I couldn’t be more happy now
There is a positive twist to the story now.
My BF and I was contacted by some other patients, asking if it was possible to get them medications for this.
So we are going to India again in a few days.
Our wish is to help others, not making money on this. We just want to help – the healthcare system in Dk can’t do anything, but we can.. and it is perfectly legal.I will of course keep on with writing
Diagnosed august 2015
Genotype 3a
Viruscount 350.000
Fibroscan 5,5December 2015 virus 190 !! Thought I was going to clear this myself
March 2016 virus 23.000
June 2016 virus 5900 going down
Fibroscan 7,7 and risingOctober – going to India to get medication Sofosbuvir and Daclatasvir
October 31. starting the treatment
Virus 69.000Friday 11. november the first bloodtest after starting the treatment
Thank you all for being concerned for others, this is amazing
Yes Donna, I will post my results when I get them…Blood on friday, results on wednesday
Diagnosed august 2015
Genotype 3a
Viruscount 350.000
Fibroscan 5,5December 2015 virus 190 !! Thought I was going to clear this myself
March 2016 virus 23.000
June 2016 virus 5900 going down
Fibroscan 7,7 and risingOctober – going to India to get medication Sofosbuvir and Daclatasvir
October 31. starting the treatment
Virus 69.000Friday 11. november the first bloodtest after starting the treatment
Hi Tommy
Crossing my fingers for you too, hope everything work out just fine for you
And thanks for the compliment (not sure this is spelled right) nice to know you understand what I am writing.
Going to the first bloodtest this friday after sterting the treatment, hoping things have gotten better.
My virus isn’t that high in the last test so I hope to clear this in the three month treatment
Diagnosed august 2015
Genotype 3a
Viruscount 350.000
Fibroscan 5,5December 2015 virus 190 !! Thought I was going to clear this myself
March 2016 virus 23.000
June 2016 virus 5900 going down
Fibroscan 7,7 and risingOctober – going to India to get medication Sofosbuvir and Daclatasvir
October 31. starting the treatment
Virus 69.000Friday 11. november the first bloodtest after starting the treatment
I tried to follow the link to write in my diagnosis and all the numbers, but for some reason my computer won’t accept it.
So maybe later on I can.But I am so happy to find this place, this site. Feeling like I am part of a community.
I am not hiding the disease for anyone, everybody around me knows this has happened. I think it is important to be open about it if it is possible.
I am aware that it is not possible to be open for everyone, but for me it is, and I am telling poeple what’s going on. But they don’t really understand what it is like, just as I wouldn’t really understand how it is to have fx a heartcondition since I never tried it myself.I am actually proud of myself for taking control. When I was diagnosed, my world fell apart and I felt like I couldn’t do anything about it, but then a wonderful nurse pointed me in the direction to India and the possibilities in bringing home my meds.
In fact, I came in contact with another patient in this process and he asked if I could bring medications home for him too, so I did, and I would do it again if someone came along and asking.
I want to help if I can, and I can totally understand if other people think it is too much to go to India to pick up their meds.And it is perfectly legal for me to do so
But for now I just feel happy to have found this site
Diagnosed august 2015
Genotype 3a
Viruscount 350.000
Fibroscan 5,5December 2015 virus 190 !! Thought I was going to clear this myself
March 2016 virus 23.000
June 2016 virus 5900 going down
Fibroscan 7,7 and risingOctober – going to India to get medication Sofosbuvir and Daclatasvir
October 31. starting the treatment
Virus 69.000Friday 11. november the first bloodtest after starting the treatment
Thanks for the nice welcome to this forum. I am still trying to find my ways around here, but can you guide me to where I write details on the condition?
I would be happy to give details and be helpful to others, I am so happy to find the help I needed when I got the diagnosis.For HepC patient in Denmark you don’t get treatment unless you are very sick. Your liver has to be extremely damaged, so you can have this condition in 20-30-40 years before they will treat you.
If we want to buy the meds outside Denmark, you can have it send to England and then go to pick it up, but it is not very secure to do it this way.
But it is legal to go to India (or where ever you can get the meds) and bring back supply for three months for yourself. So we did this, but it was difficult to figure out where to get it, who to trust, finding someone here in Dk who took the same journey we did.
But we succeeded and if I can help other patient with this, I sure would do so.The meds cost us around 2000 US dollars pr person and we got from Delhi
Diagnosed august 2015
Genotype 3a
Viruscount 350.000
Fibroscan 5,5December 2015 virus 190 !! Thought I was going to clear this myself
March 2016 virus 23.000
June 2016 virus 5900 going down
Fibroscan 7,7 and risingOctober – going to India to get medication Sofosbuvir and Daclatasvir
October 31. starting the treatment
Virus 69.000Friday 11. november the first bloodtest after starting the treatment
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