I think Russell must've lost his screen name and password! Either that or he didn't find our form of humorous support very meaningful! Nah..... Couldn't be true
Well they say laughter is the best medicine. I don't think it contains any antiviral properties however so I will stick with the Harvoni.
Personally I think Dragons want us to be fearful.
Tig said
Apr 19, 2016
I think Russell must've lost his screen name and password! Either that or he didn't find our form of humorous support very meaningful! Nah..... Couldn't be true
JimmyK said
Apr 19, 2016
russell b wrote:
im hopeing to have a meaningful discussion with anyone with hep c
Ok not sure about one as my stuff may or not be meaningful with regard to significant. And I often employ language that lacks in relevant or important substance so not doing real good on the one request but with regard to discussion , well I am full of it!
Oh wait.
-- Edited by JimmyK on Tuesday 19th of April 2016 07:02:32 PM
Sydhanrahan said
Apr 19, 2016
Give us an update Russell or am I just looking in the wrong place?
Syd
RAGDOLL said
Mar 26, 2016
Welcome Russell, as mentioned by others, when you share your specifics there are a lot of experienced and educated people available in this forum to help you with your journey with Hep C.
Chris
Shadowfax said
Mar 26, 2016
Welcome Russell,
I am pretty sure you will find all the information you could possibly want in this forum. We are glad you found us. As mentioned, please tell us a bit more about yourself so people can respond accordingly.
Take care
SF
Cinnamon Girl said
Mar 26, 2016
Hello Russell, welcome!
I`m glad you stumbled upon this forum, you`ve found a safe haven for anyone who is affected by Hep C, you can relax and speak freely here, you`re with friends.
Once we know a few more details about your Hep C history and circumstances we`ll be happy to share all the information you`re looking for. Feel free to have a good look around, and ask any questions that might be bothering you, someone will always reply.
Looking forward to hearing back from you...
Sydhanrahan said
Mar 26, 2016
Hi Russell,
there is lots of help and support on this site from people who are, or have been, on the same journey as you.
Also while you're getting to know other people you will learn a lot about your liver, its functions, what symptoms, if any, others have.
Glad you have found the forum and hoping to hear your story soon.
Syd
Linuxter said
Mar 25, 2016
Hi Russell,
Welcome to the forum, this a great place, lots of great, up-to-date information, very friendly family here.
I'm on treatment now, you'll find people in all stages, pre-treatment, on-treatment and post-treatment.
We've all been right where you are now, do tell us a little about your diagnosis.
Dave
wmlj1960 said
Mar 25, 2016
Hi Russell and welcome from me as well.
If your looking for conversation about hep c then you have hit the jackpot. We have many active members who are affected by hep c and either looking for information about a cure, presently on treatment, or have been cured. There is an abundance of knowledge and plenty of support here for you.
What is your current situation as it relates to hep c? Are you planning to start treatment? Have you ever been treated in the past? Do you have any lab results you can share with us or have any questions we can help you with?
I understand about feeling down. We've been right where you are but there is a solution and you can look forward to better days ahead. I just completed treatment ~3 months ago and I feel better than I ever remember feeling and it's getting better every day.
Others will be along to welcome you as well so make yourself comfortable. We are glad you found us.
robertsamx said
Mar 25, 2016
Welcome to the forum Russell. You sound a little down ? tell us a little about yourself and let's see if we can help. Take a look at my signature line on this post, it's at the bottom of this message , it tells you a little about me and where I'm at in dealing with the hep c thing .RC
Tig said
Mar 25, 2016
Hi Russell,
Welcome Brother! Glad you found us and invite you to tell us a little about yourself. I'm leaving a link and ask that you provide some info in your signature line. That's the info you see at the bottom of most members posts. Things like your history, genotype, fibrosis, previous treatment, etc. You have 220 characters to share your story and it helps us reply to your questions and concerns!
You have found an awesome group and we're here to help and inform. I'm glad you're here!
Well they say laughter is the best medicine. I don't think it contains any antiviral properties however so I will stick with the Harvoni.
Personally I think Dragons want us to be fearful.
I think Russell must've lost his screen name and password! Either that or he didn't find our form of humorous support very meaningful! Nah..... Couldn't be true
ADJECTIVE
NOUN
-- Edited by JimmyK on Tuesday 19th of April 2016 07:02:32 PM
Give us an update Russell or am I just looking in the wrong place?
Syd
Welcome Russell, as mentioned by others, when you share your specifics there are a lot of experienced and educated people available in this forum to help you with your journey with Hep C.
Chris
Welcome Russell,
I am pretty sure you will find all the information you could possibly want in this forum. We are glad you found us. As mentioned, please tell us a bit more about yourself so people can respond accordingly.
Take care
SF
Hello Russell, welcome!
I`m glad you stumbled upon this forum, you`ve found a safe haven for anyone who is affected by Hep C, you can relax and speak freely here, you`re with friends.
Once we know a few more details about your Hep C history and circumstances we`ll be happy to share all the information you`re looking for. Feel free to have a good look around, and ask any questions that might be bothering you, someone will always reply.
Looking forward to hearing back from you...
Hi Russell,
there is lots of help and support on this site from people who are, or have been, on the same journey as you.
Also while you're getting to know other people you will learn a lot about your liver, its functions, what symptoms, if any, others have.
Glad you have found the forum and hoping to hear your story soon.
Syd
Hi Russell,
Welcome to the forum, this a great place, lots of great, up-to-date information, very friendly family here.
I'm on treatment now, you'll find people in all stages, pre-treatment, on-treatment and post-treatment.
We've all been right where you are now, do tell us a little about your diagnosis.
Dave
Hi Russell and welcome from me as well.
If your looking for conversation about hep c then you have hit the jackpot. We have many active members who are affected by hep c and either looking for information about a cure, presently on treatment, or have been cured. There is an abundance of knowledge and plenty of support here for you.
What is your current situation as it relates to hep c? Are you planning to start treatment? Have you ever been treated in the past? Do you have any lab results you can share with us or have any questions we can help you with?
I understand about feeling down. We've been right where you are but there is a solution and you can look forward to better days ahead. I just completed treatment ~3 months ago and I feel better than I ever remember feeling and it's getting better every day.
Others will be along to welcome you as well so make yourself comfortable. We are glad you found us.
Welcome to the forum Russell. You sound a little down ? tell us a little about yourself and let's see if we can help. Take a look at my signature line on this post, it's at the bottom of this message , it tells you a little about me and where I'm at in dealing with the hep c thing .RC
Hi Russell,
Welcome Brother! Glad you found us and invite you to tell us a little about yourself. I'm leaving a link and ask that you provide some info in your signature line. That's the info you see at the bottom of most members posts. Things like your history, genotype, fibrosis, previous treatment, etc. You have 220 characters to share your story and it helps us reply to your questions and concerns!
You have found an awesome group and we're here to help and inform. I'm glad you're here!
http://hepcfriends.activeboard.com/t58862021/how-to-create-your-signature-forum-abbreviation-definitions/
new to this chat room and its the first room i have ever joind boy what a pain in the arss.
im hopeing to have a meaningful discussion with anyone with hep c
im feeling a little down today and could rely use a helping hand.