Hepatitis C Support Group
Hepatitis C is a blood-borne viral disease which can cause liver inflammation, fibrosis, cirrhosis and liver cancer. The hepatitis C virus (HCV) is spread by blood-to-blood contact with an 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.
Most people don't understand hepatitis C and cannot imagine what living with a chronic illness means. With the hope that there are some who wish to understand, these are some of the things I'd like you to know about us.
Please understand that being sick doesn't mean we are not still human with all the same emotions that healthy people experience. Some of us must spend our time carefully so that we conserve what little energy we possess. If you visit we may not be much fun, but we still love and appreciate company. Some of us worry about our jobs, schooling and families. Most of the time we'd like to hear what is going on in your life as well as sharing our lives.
Please understand that one can be happy but not healthy. When you have the flu you feel fairly miserable, but we've been ill for years. We can't be miserable all the time, in fact most of us work hard at not being miserable. So when you speak with us and we sound happy, it means we are happy. That's all. It doesn't mean we are not sick, in pain and extremely fatigued, or that a miracle cure has been found and we are all healthy once again. Please don't say, "Oh you're sounding better!" We are not sounding better, we are sounding happy. Feel free to remark about our happiness. Just don't assume that it means we are better.
Please understand that being able to stand up and participate in an activity for 15 or 20 minutes, doesn't necessarily mean that we can participate for 30 minutes or an hour. It's quite likely that doing that 15 minutes has exhausted our resources and we may need time to recover. Remember the last time you played a swift game of tennis or softball. You couldn't repeat that feat over and over again. This applies to every thing we do.
Please understand that chronic illness is variable. It's quite possible that one day we are able to walk to the park, or shop in the mall, while the next day we may have no energy at all. Please don't say, "But you did it yesterday." If you want us to do something, just ask and we will tell you if we are able. If it is necessary to cancel an appointment with you at the last moment , please don't take it personally. There are days when we feel great and all of a sudden that changes and the fatigue is overwhelming.
Please don't ask us how we got this disease. There are many ways to acquire hepatitis C. Some of us made a foolish choice to experiment with IV drugs when we were young and invincible. Some of us were born with hemophilia and need to use blood products to stay alive. Some of us were given blood transfusions before 1992. Some of us are veterans who fought proudly for our country and some of us are kidney dialysis patients as well. Many of us have no risk factors at all and do not know where we got hepatitis C. If we wish to share our medical history with you, we will. Please don't be afraid to hug us, kiss us or hold us. You cannot "catch" hepatitis C from us unless there was a mixing of our blood with yours.
Please understand if we tell you that we have to sit down, lie down or take our meds, that we have to do it now. Chronic illness doesn't wait for a convenient time. It does not feel good to have to stop what we are doing to tend to our health. Remember that we didn't ask for this. We mourn for our lives before illness, when we were free to pursue all our dreams and hopes. We hope you understand.
from:hepcfoundation
PRINT AND SHARE WITH FAMILY & FRIENDS, WE DID!
Please understand that being sick doesn't mean we are not still human with all the same emotions that healthy people experience. Some of us must spend our time carefully so that we conserve what little energy we possess. If you visit we may not be much fun, but we still love and appreciate company. Some of us worry about our jobs, schooling and families. Most of the time we'd like to hear what is going on in your life as well as sharing our lives.
Please understand that one can be happy but not healthy. When you have the flu you feel fairly miserable, but we've been ill for years. We can't be miserable all the time, in fact most of us work hard at not being miserable. So when you speak with us and we sound happy, it means we are happy. That's all. It doesn't mean we are not sick, in pain and extremely fatigued, or that a miracle cure has been found and we are all healthy once again. Please don't say, "Oh you're sounding better!" We are not sounding better, we are sounding happy. Feel free to remark about our happiness. Just don't assume that it means we are better.
Please understand that being able to stand up and participate in an activity for 15 or 20 minutes, doesn't necessarily mean that we can participate for 30 minutes or an hour. It's quite likely that doing that 15 minutes has exhausted our resources and we may need time to recover. Remember the last time you played a swift game of tennis or softball. You couldn't repeat that feat over and over again. This applies to every thing we do.
Please understand that chronic illness is variable. It's quite possible that one day we are able to walk to the park, or shop in the mall, while the next day we may have no energy at all. Please don't say, "But you did it yesterday." If you want us to do something, just ask and we will tell you if we are able. If it is necessary to cancel an appointment with you at the last moment , please don't take it personally. There are days when we feel great and all of a sudden that changes and the fatigue is overwhelming.
Please don't ask us how we got this disease. There are many ways to acquire hepatitis C. Some of us made a foolish choice to experiment with IV drugs when we were young and invincible. Some of us were born with hemophilia and need to use blood products to stay alive. Some of us were given blood transfusions before 1992. Some of us are veterans who fought proudly for our country and some of us are kidney dialysis patients as well. Many of us have no risk factors at all and do not know where we got hepatitis C. If we wish to share our medical history with you, we will. Please don't be afraid to hug us, kiss us or hold us. You cannot "catch" hepatitis C from us unless there was a mixing of our blood with yours.
Please understand if we tell you that we have to sit down, lie down or take our meds, that we have to do it now. Chronic illness doesn't wait for a convenient time. It does not feel good to have to stop what we are doing to tend to our health. Remember that we didn't ask for this. We mourn for our lives before illness, when we were free to pursue all our dreams and hopes. We hope you understand.
from:hepcfoundation
PRINT AND SHARE WITH FAMILY & FRIENDS, WE DID!
Great to give to your boss, or family when you are starting treatment.
God Bless you sweetie and may you always be as beautiful as you are now.
I have no problem telling people that I have Hep C, in fact I often find it important. Something as small as using my tweezers can cause future havoc in somebodys life. I also do not hide how I got it, which was by sharing needles. That was my past (35 years ago) which is a part of my life story. Although it's nothing to boast about, I forgave myself, learned from it, and moved on. I was told by a public health nurse that being that I feel so tired, etc., now, I may feel much better after I start treatment. Ohhh . . . I hope so!
I know I did, I was totally fed up of telling the same old story time after time, so print and give out to those you see often.
Mck