Aa
My spouse and some of my friends just don't get what treatment means
I must be feeling like sharing today so tell me to shut up if I'm posting too much.
During my original tx on SOC, my wife, who I love with all my heart, just didn't get that I felt like poop and couldn't do many of the activities that I did before. On shot night she seemed annoyed that I was sensitive to light and sounds and just wanted to curl up in a ball in a quiet environment. When I told her that I was accepted into Prove 3 she said that it's my decision but I better act normal around her and the kids.
All of this is very usual because we have a child with a life threatening disease. From the day of his diagnosis we've been very supportive of him, each other and channeled our grief into raising funds for the cure for his disease. Daily we share in his care giving and therapies.
Next when I told my best friend that I was going to do the Prove 3 trial he changed the topic and acted like I was opting for some kind of elective cosmetic surgery of something. He didn't want to talk about it further.
I've shared my HCV status with very few people and how my wife and best friend reacted really confused me and hurt. Last year I had another best friend die of brain cancer that took about a year between diagnosis and his death. I called or wrote him several times per week and made several out of state trips just to touch base and make sure that he knew what his friendship meant to me.
So, as I start into the Prove 3 trial I''ve said very little to my wife about how I'm feeling and pretend with my friend that I'm not even going through treatment again. I'm not doing this our of anger but more out of confusion.
Have any of you experienced these kind of reactions from loved ones and how are you dealing with it?
Mike
During my original tx on SOC, my wife, who I love with all my heart, just didn't get that I felt like poop and couldn't do many of the activities that I did before. On shot night she seemed annoyed that I was sensitive to light and sounds and just wanted to curl up in a ball in a quiet environment. When I told her that I was accepted into Prove 3 she said that it's my decision but I better act normal around her and the kids.
All of this is very usual because we have a child with a life threatening disease. From the day of his diagnosis we've been very supportive of him, each other and channeled our grief into raising funds for the cure for his disease. Daily we share in his care giving and therapies.
Next when I told my best friend that I was going to do the Prove 3 trial he changed the topic and acted like I was opting for some kind of elective cosmetic surgery of something. He didn't want to talk about it further.
I've shared my HCV status with very few people and how my wife and best friend reacted really confused me and hurt. Last year I had another best friend die of brain cancer that took about a year between diagnosis and his death. I called or wrote him several times per week and made several out of state trips just to touch base and make sure that he knew what his friendship meant to me.
So, as I start into the Prove 3 trial I''ve said very little to my wife about how I'm feeling and pretend with my friend that I'm not even going through treatment again. I'm not doing this our of anger but more out of confusion.
Have any of you experienced these kind of reactions from loved ones and how are you dealing with it?
Mike
Hi, folks,
Since this thread is old and the original participants are no longer taking part, we'll close it now. If you'd like to ask a question or start a new thread, please click the "Post a Question" button near the top of this page. Thanks!
Claire
______________________________________________________
******** CLOSED DISCUSSION ********
No more comments, please.
______________________________________________________
Since this thread is old and the original participants are no longer taking part, we'll close it now. If you'd like to ask a question or start a new thread, please click the "Post a Question" button near the top of this page. Thanks!
Claire
______________________________________________________
******** CLOSED DISCUSSION ********
No more comments, please.
______________________________________________________
i know that this is to be your second time around.
though in afterthough i am not certain how well it was recieved. i did explain to those i cared to, that this is chemotherapy, the drugs used are also used for leukemia - blood cancer. that the medicines used do several things, one speeds up lysis which is red cell death a natural occurance but at a much accellerated rate, another drug attacks the virus its self (if i recall correctly while it was freed fromd the early cell death. this process leaving us anemic most are then prescribe the drug to stimulate bone marrow to release new cells. each drug has its own side effect, ..explained the symptoms,
they seemed to understand, but when they actually see it.. well different story sometimes helpful, understanding sometimes not. they missed the fact that i could not cook, rarely cleaned, saw my homebound as opportunity to offer more rides when needed..
though in afterthough i am not certain how well it was recieved. i did explain to those i cared to, that this is chemotherapy, the drugs used are also used for leukemia - blood cancer. that the medicines used do several things, one speeds up lysis which is red cell death a natural occurance but at a much accellerated rate, another drug attacks the virus its self (if i recall correctly while it was freed fromd the early cell death. this process leaving us anemic most are then prescribe the drug to stimulate bone marrow to release new cells. each drug has its own side effect, ..explained the symptoms,
they seemed to understand, but when they actually see it.. well different story sometimes helpful, understanding sometimes not. they missed the fact that i could not cook, rarely cleaned, saw my homebound as opportunity to offer more rides when needed..
WOW! what a thread... I mean this is the second longest thread I've seen since posting and covering so much. I don't know about the rest but I'm feeling Good.
jasper
jasper
I was so overwhelmed reading this entire post, that I had to have a small cry. I am one week post treatment.(48 weeks) I am 64 and have completely accepted the possibility that I may not live a lot longer. I felt that doing the tx was owed to my loved ones. I didn't want them to witness the family oldest, giving up, or losing without the same fight I would want from them. Quiting, slitting my wrists, killing anyone, was not an option. As, all of you have said, the sx are impossible to explain to anyone. Most people I have come across seem that think I am having a tx that resembles a very long flu.
My mental disorder from this tx had been the hardest to bear. It is impossible to explain "mind fog" which is a benign way of saying "insane" to me. And it hasn't even begun to leave. I can't make decisions without some notice that I'm going to need to. Just last night at a dinner with some of my adult grandchildren, the menu made no sense to me whatsoever. My grandaughter kindly asked some simple questions to make it possible to order. It was the end to the day, I couldn't think and I was worried about my abillity to get back to the car. My sister with whom I live, as I can't do much for myself, will ask what I want from the store. This is an impossible question to answer. I can't even begin to figure it out unless she says she will go in one half hour to give me time to think. Then the overwhelm passes and in 5 minuets or so, my brain kicks into a more normal mode and I can make a list.
I do however, have relatives that not only do not understand, but have put me through such hell that I don't know if I can ever have a relationship with them again. Making demands of my time, boldly pointing out my undeserved self centered refusals. Pushing relentlessly until I felt helpless and would have to give in and do what was wanted. One time I was in bed for a month afterwards, too weak to dress or bath often enough. (I couldn't get out of a tub, and it is too dangerous to stand and shower as I will fall.) I cried and raged, cried and raged untill indeed I was insane. And still, I haven't killed a soul.
The accusing emails still continue. They ask questions like, don't I know they know I'm sick? Who do I think they are? That's why they gave me a heads up about going to the bank for them NEXT friday, not tomorrow. geeze ! How insensitive do I think they are?
Please..... it make me ill to even think about this ongoing hell, centered around my fathers care,(read money, money, money) which I have been responsible for the last 7 years, until I became too sick last year.
THERE, I HAVE UNLOADED FOR THE FIRST TIME ON PEOPLE WHO KNOW WHAT I AM TALKING ABOUT. There is always more to complain about, but this was enough to help me feel centered again, and can continue. And forgive. But the relationship is ruined and gone forever. And I don't feel one ounce of regret, shoud have done it years ago. God bless you all and thank you over and over for being there.
susan
My mental disorder from this tx had been the hardest to bear. It is impossible to explain "mind fog" which is a benign way of saying "insane" to me. And it hasn't even begun to leave. I can't make decisions without some notice that I'm going to need to. Just last night at a dinner with some of my adult grandchildren, the menu made no sense to me whatsoever. My grandaughter kindly asked some simple questions to make it possible to order. It was the end to the day, I couldn't think and I was worried about my abillity to get back to the car. My sister with whom I live, as I can't do much for myself, will ask what I want from the store. This is an impossible question to answer. I can't even begin to figure it out unless she says she will go in one half hour to give me time to think. Then the overwhelm passes and in 5 minuets or so, my brain kicks into a more normal mode and I can make a list.
I do however, have relatives that not only do not understand, but have put me through such hell that I don't know if I can ever have a relationship with them again. Making demands of my time, boldly pointing out my undeserved self centered refusals. Pushing relentlessly until I felt helpless and would have to give in and do what was wanted. One time I was in bed for a month afterwards, too weak to dress or bath often enough. (I couldn't get out of a tub, and it is too dangerous to stand and shower as I will fall.) I cried and raged, cried and raged untill indeed I was insane. And still, I haven't killed a soul.
The accusing emails still continue. They ask questions like, don't I know they know I'm sick? Who do I think they are? That's why they gave me a heads up about going to the bank for them NEXT friday, not tomorrow. geeze ! How insensitive do I think they are?
Please..... it make me ill to even think about this ongoing hell, centered around my fathers care,(read money, money, money) which I have been responsible for the last 7 years, until I became too sick last year.
THERE, I HAVE UNLOADED FOR THE FIRST TIME ON PEOPLE WHO KNOW WHAT I AM TALKING ABOUT. There is always more to complain about, but this was enough to help me feel centered again, and can continue. And forgive. But the relationship is ruined and gone forever. And I don't feel one ounce of regret, shoud have done it years ago. God bless you all and thank you over and over for being there.
susan
Today feels like a new day. Yesterday when I posted this topic I had no idea of the responses that I would receive. Honestly thanks for being there when I really needed to talk this out.
Those of you who know me through posting here know that I'm tyically factual and focused on HCV information. I'm not embarassed that I opened up to you guys but I sure am surprised and happy at your support and caring attitudes.
One of my biggest motivations for treating again is to someday see my daughter marry a man who deserves her, The other big motivation is to continue the fight to find the cure for Cystic Fibrosis and see my son live a long and healthy life.
We have a huge group of family and friends who have raised large amounts of money for the research for the cure for CF, which like HCV is also getting closer. Unlike HCV with 200M afflicted people, there are only 30,000 kids with Cystic Fibrosis so the drug companies won't invest in the cure because of profit motives (which is understandable). It is our money that we raised that funded Vertex to produce the VX-770 compound that is showing so much promise and is now in Phase II clinical trials and fast-tracked by the FDA. Wouldn't it be something if Vertex saved both my son and me?
When the time is right 'm going to ask my wife to read this post in its entirety. Your thoughts and insights should mean a lot to her.
Thanks and God bless us all with a cure in the near future.
Mike
Those of you who know me through posting here know that I'm tyically factual and focused on HCV information. I'm not embarassed that I opened up to you guys but I sure am surprised and happy at your support and caring attitudes.
One of my biggest motivations for treating again is to someday see my daughter marry a man who deserves her, The other big motivation is to continue the fight to find the cure for Cystic Fibrosis and see my son live a long and healthy life.
We have a huge group of family and friends who have raised large amounts of money for the research for the cure for CF, which like HCV is also getting closer. Unlike HCV with 200M afflicted people, there are only 30,000 kids with Cystic Fibrosis so the drug companies won't invest in the cure because of profit motives (which is understandable). It is our money that we raised that funded Vertex to produce the VX-770 compound that is showing so much promise and is now in Phase II clinical trials and fast-tracked by the FDA. Wouldn't it be something if Vertex saved both my son and me?
When the time is right 'm going to ask my wife to read this post in its entirety. Your thoughts and insights should mean a lot to her.
Thanks and God bless us all with a cure in the near future.
Mike
sorry to hear about the lack of support. When I was on tx some people that I expected very little support from ended up being the most supportive and visa versa....My philosophy in life (really helped my while on tx and in other situations) which may be helpful for you to think about is...
1. Draw upon people who offer you support now and have done so in the past
2. Dont ask people that have not offered/ or refused you support in the past (or presently) for help, you are setting them and yourself up for a painful situation
3. Put as much distance as possible between yourself and people that are hurtful to you
Have you thought about trying to find a support group? Personal counselling? You really should be talking to someone about how you are feeling...what you are going through can be so isolating
warm thoughts
Sarah
1. Draw upon people who offer you support now and have done so in the past
2. Dont ask people that have not offered/ or refused you support in the past (or presently) for help, you are setting them and yourself up for a painful situation
3. Put as much distance as possible between yourself and people that are hurtful to you
Have you thought about trying to find a support group? Personal counselling? You really should be talking to someone about how you are feeling...what you are going through can be so isolating
warm thoughts
Sarah
I was looking to see if someone posted that poem.
That was from a posting to cheer me up when my husband was being a bugar. It's
a little depressing,but it's true. I let my husband read that. What a slap in his face to realize what we go through.
A perfect poem. Helped me to know my pain was normal and that I wasn't the only one. Some get lucky, but so many aren't.
Thank you
Missy
That was from a posting to cheer me up when my husband was being a bugar. It's
a little depressing,but it's true. I let my husband read that. What a slap in his face to realize what we go through.
A perfect poem. Helped me to know my pain was normal and that I wasn't the only one. Some get lucky, but so many aren't.
Thank you
Missy
This is apparently a very big subject that alot of us share. I'm really sorry
for what your wife said. It could be very overwhelming for her to have you sick again. I believe it will work out for you. She'll come around and realize
you need her. Try to be patient and by all means let her know how you feel
and let her do the same.
My husband really hurt me in the beginning. I guess we both thought I'd get through this and in 2wks I'd be fine. I just didn't realize how insufferable this tx is. The point is, neither does anyone else. My Dr. put it out to us as if it were no big deal and within 2 wks I'd be fine. WRONG!
My husband has seen me go through this for 10 wks now. He sees me trying to get past the pain/fatigue/fevers. I really try and he knows this. Finally I got his understanding. I don't ask for a pity party, but I do expect understanding.
FEMALE/RIBA= Explosives
Because you've been through this before it kind of shocked me your wife stated
as she did. Do remind her of what you're going through and tell her your sorry
that this is hard for her,but this is something that has to be done and how important it is for you to be a strong person to get through this and to see her upset brings you down. You'll need all the forces you can get. This time you are going to win!
Your child,well that's a given. Lots of hugs! I don't know how old he is.
Teenagers get a little weird about that. Spend quality time with him as much as possible , as I'm sure this will help you feel better.
As far as your friend, again until you walk in our shoes, they'll never get it.
In the mean time you can come here when needed where we know what you're going through.
Be strong and stay busy 22 wks will fly.
Missy
for what your wife said. It could be very overwhelming for her to have you sick again. I believe it will work out for you. She'll come around and realize
you need her. Try to be patient and by all means let her know how you feel
and let her do the same.
My husband really hurt me in the beginning. I guess we both thought I'd get through this and in 2wks I'd be fine. I just didn't realize how insufferable this tx is. The point is, neither does anyone else. My Dr. put it out to us as if it were no big deal and within 2 wks I'd be fine. WRONG!
My husband has seen me go through this for 10 wks now. He sees me trying to get past the pain/fatigue/fevers. I really try and he knows this. Finally I got his understanding. I don't ask for a pity party, but I do expect understanding.
FEMALE/RIBA= Explosives
Because you've been through this before it kind of shocked me your wife stated
as she did. Do remind her of what you're going through and tell her your sorry
that this is hard for her,but this is something that has to be done and how important it is for you to be a strong person to get through this and to see her upset brings you down. You'll need all the forces you can get. This time you are going to win!
Your child,well that's a given. Lots of hugs! I don't know how old he is.
Teenagers get a little weird about that. Spend quality time with him as much as possible , as I'm sure this will help you feel better.
As far as your friend, again until you walk in our shoes, they'll never get it.
In the mean time you can come here when needed where we know what you're going through.
Be strong and stay busy 22 wks will fly.
Missy
I'm sorry you're not getting the support you need right now.
It must be overwhelming for your wife to consider having both you on treatment and caring for your son right now. I'm sure she feels scared and wonders how she can handle all this.
Going with you to the doctor and reading about this (perhaps on this forum) should help her understand that YOU'RE going through a lot right now.
Also, she needs to focus on the fact that after your treatment she will have a healthy husband to share fully in the bringing up and care of your son.
Treating for 24 weeks is not that long, it goes by quickly, and before you know it you will be through.
I'm sure you've talked it through, but perhaps talking to a counselor or therapist before you treat will help her express her feelings and fears, and she can get help putting everything in perspective.
But whatever happens, congratulations on going ahead and treating even in the face of these very real obstacles. You have every right to take care of your own health no matter how difficult it is on those around you. Keep coming here for support.
It must be overwhelming for your wife to consider having both you on treatment and caring for your son right now. I'm sure she feels scared and wonders how she can handle all this.
Going with you to the doctor and reading about this (perhaps on this forum) should help her understand that YOU'RE going through a lot right now.
Also, she needs to focus on the fact that after your treatment she will have a healthy husband to share fully in the bringing up and care of your son.
Treating for 24 weeks is not that long, it goes by quickly, and before you know it you will be through.
I'm sure you've talked it through, but perhaps talking to a counselor or therapist before you treat will help her express her feelings and fears, and she can get help putting everything in perspective.
But whatever happens, congratulations on going ahead and treating even in the face of these very real obstacles. You have every right to take care of your own health no matter how difficult it is on those around you. Keep coming here for support.
It's really tough dealing with this aspect of the disease. I think people understand and relate to cancer in a way they can't to Hepatitis C. Most people don't know what to say to someone who is doing treatment. Maybe they're afraid of saying the wrong thing or illness makes them uncomfortable.
miked-I run too, and managed to throughout treatment until the last 6 weeks when it got to be more of a shuffle. I knew it was time to start walking instead when I got passed by a walker one day when I was "running" up hill! It wasn't easy, but it helped to keep something in my life that was a part of my normal routine prior to treatment.
Good luck with your 2nd try for SVR.
miked-I run too, and managed to throughout treatment until the last 6 weeks when it got to be more of a shuffle. I knew it was time to start walking instead when I got passed by a walker one day when I was "running" up hill! It wasn't easy, but it helped to keep something in my life that was a part of my normal routine prior to treatment.
Good luck with your 2nd try for SVR.
I also want to say that I have great admiration for you and your wife. Dealing with one serious health problem is very difficult. I can only imagine what two familiy members with problems must be like.
You must be a very strong family to be able to handle that. I am sure that strength will work in your favor.
You must be a very strong family to be able to handle that. I am sure that strength will work in your favor.
Thank you for that. There is also a poem someone posted recently. :
If It Don't Show Today
I have had quite a few people
come up to me and say
why you're looking pretty good
you don't seem sick today
Well, have you ever lived wondering if
each day will be your last
not knowing if there's a tomorrow and
reliving and regretting your past
Have you ever fought daily just
to get out of your bed
had a foggy grey cloud hanging always
over your head
Have you ever lost 30lbs or
had your hair all fall out
wasted away in a chair
with no one about
Oh I have my good days too
when I don't let it show
and some see me those days only
so they don't really know
So all you nonheppers out there who
haven't ever felt this way
don't ask are you really sick if
I don't show it today....
J.W. Cutrer
aka SirJohn
If It Don't Show Today
I have had quite a few people
come up to me and say
why you're looking pretty good
you don't seem sick today
Well, have you ever lived wondering if
each day will be your last
not knowing if there's a tomorrow and
reliving and regretting your past
Have you ever fought daily just
to get out of your bed
had a foggy grey cloud hanging always
over your head
Have you ever lost 30lbs or
had your hair all fall out
wasted away in a chair
with no one about
Oh I have my good days too
when I don't let it show
and some see me those days only
so they don't really know
So all you nonheppers out there who
haven't ever felt this way
don't ask are you really sick if
I don't show it today....
J.W. Cutrer
aka SirJohn
I think it all has been said in the earlier posts. I can only say that my experience was often like yours and theirs (I have done this a few times). While I was still working, I once posted the interferon warnings on the company email system. I highlighted suicidal ideation and homicidal ideation (as a joke). I got many funny responses about people refusing to be in the same room as me and having a rule that I could only teleconference until my treatment ended.
After a while, they actually became sympathetic and made life a little easier. I gave my wife a lot of literature and asked her to read this board; she is much more understanding now.
Today I had a wonderful experience: spring is sailboat commissioning time and for a sailor like me, this is one of the most exciting times of the year. This year, I am felling so sick that I didn't have a clue how I would get the boat ready for launching. Yesterday my wife and best friend said that they would accompany me to the boat, and I should only supervise while they did all the work!
This is my 5th time on treatment and I finally have support. Perhaps it is because as I age, I look worse while I am treating. When I first treated, most people said I looked better than normal even though I felt worse. Now people meet me and look worried when the see me for the first time in a while.
I am sure things will improve for you and I certainly hope the new drug works well for your son .
After a while, they actually became sympathetic and made life a little easier. I gave my wife a lot of literature and asked her to read this board; she is much more understanding now.
Today I had a wonderful experience: spring is sailboat commissioning time and for a sailor like me, this is one of the most exciting times of the year. This year, I am felling so sick that I didn't have a clue how I would get the boat ready for launching. Yesterday my wife and best friend said that they would accompany me to the boat, and I should only supervise while they did all the work!
This is my 5th time on treatment and I finally have support. Perhaps it is because as I age, I look worse while I am treating. When I first treated, most people said I looked better than normal even though I felt worse. Now people meet me and look worried when the see me for the first time in a while.
I am sure things will improve for you and I certainly hope the new drug works well for your son .
For those who can maintain their regular activity levels while on tx, God bless you. I couldn't and got fired. I did learn from both times on tx that the people you work with, even your loved ones, are accustomed to you meeting your responsibilities and obligations. Once they see you can't, attitudes will change. Once they go through their phases of shock, anger, pity and acceptance they get to the point of wanting it to be over for you. I don't mean death. They get weary for us and don't know what to do or say. The first time I was on tx I did not include my wife in any part of my tx. She is much like your wife. She holds everything in and maintains a positive attitude for her and the kids. This I am very grateful for, but the sx can be overwhelming at times. This 2nd time around I made sure she went with me to my Dr's appointments. This has helped a great deal. I have made sure she is my partner in this personal hell.
Hope this helps you and others.
Hope this helps you and others.
yalls comments confirm the positve aspects of my strategy. i have told virtually no one about my disaster, especially not my family. i didnt tell them because i knew it might play out for many years. why drag them through it? i didnt tell anyone else because of the anticipated lack of understanding. it is simply true that until youve been here, it is all meaningless. i beleive, too, that to survive this you must have a least one person to talk to who at least acts like they understand. my plan of solitary confinement may be lonlier but its easier, you dont have to worry about others disappointing you along the way.
Your hermit comment really rang true. When I last treated I avoided social situations like the plague. We're big-time hockey fans but just the idea of being in the area with the horns and music blowing at goals just about drove me nuts.
I too take comfort in my gardening which for the Prove 3 trial will be in the summer. It's peaceful and feels productive to plant something that you know is for the future. Right now we're pigging out on Asparagus.
Thanks everyone. I really do feel better for talking (writing) this out today.
I too take comfort in my gardening which for the Prove 3 trial will be in the summer. It's peaceful and feels productive to plant something that you know is for the future. Right now we're pigging out on Asparagus.
Thanks everyone. I really do feel better for talking (writing) this out today.
"once treatment is over and the "old you" returns that friends and family will be back, I found that out. Thing is how many of them do you really want back. Sorry for the cynicism but wanted to let you know that you're not alone."
Just call me cynical. And I don't (want them back).
wyntre
Just call me cynical. And I don't (want them back).
wyntre
I'm so sorry that you have had little or no understanding from your wife and best friend re: your treatment. It's very hard for many people to understand what we are going through that's why these support forums are so wonderful.
My younger son and his wife wouldn't even let me hold me new grandbaby for a couple months because they thought I was contagious. I had to have the doctor send them all this stuff on how you get hep. C. You cannot get it casually. Many people have hep. B and C mixed up or Hep. C and HIV.
There are brochures at the doctor's office you can give your wife and friend, etc. That explain better what we are going through and why sometimes we feel so badly. I hope you can get some of them. This is not the flu.
My younger son and his wife wouldn't even let me hold me new grandbaby for a couple months because they thought I was contagious. I had to have the doctor send them all this stuff on how you get hep. C. You cannot get it casually. Many people have hep. B and C mixed up or Hep. C and HIV.
There are brochures at the doctor's office you can give your wife and friend, etc. That explain better what we are going through and why sometimes we feel so badly. I hope you can get some of them. This is not the flu.
were here for ya buddy and each other. Yup!, same reaction from sisters. Ho well ****'em I'm living for me cuz me is the only one I got.
jasper
jasper
Gee, it must be tough living with someone who is probably in denial about how bad you feel. My husband is supportive though he's having a tough time with my emotions.
Two weeks ago I had a huge argument with my sister. She is a social butterfly and always tries to get me to participate. So I've tried to tell her, unlike others close to me, just how badly the side effects of tx are. She just couldn't accept it. In her mind, I am fine, I couldn't be sick.
SO when she told me she needed me to housesit for her and check in on my mom, while she went to Italy for 3 weeks, I lost it. I went ballistic, asked my sister if she would be asking favors of me, if I was undergoing chemo for cancer. AND my doc says this is what tx is like.
It is difficult. My friends are great but for the most part, I've become a hermit. I just want to be left alone, grow my flowers and read my book. I hope you can find a way to reassure your wife while letting her know that you need her support. Best of luck. OH
Two weeks ago I had a huge argument with my sister. She is a social butterfly and always tries to get me to participate. So I've tried to tell her, unlike others close to me, just how badly the side effects of tx are. She just couldn't accept it. In her mind, I am fine, I couldn't be sick.
SO when she told me she needed me to housesit for her and check in on my mom, while she went to Italy for 3 weeks, I lost it. I went ballistic, asked my sister if she would be asking favors of me, if I was undergoing chemo for cancer. AND my doc says this is what tx is like.
It is difficult. My friends are great but for the most part, I've become a hermit. I just want to be left alone, grow my flowers and read my book. I hope you can find a way to reassure your wife while letting her know that you need her support. Best of luck. OH
people have such a lack of understanding - despite explaining the disease and what to expect. i thought this would have garnered some kind of understanding or support, i felt very alone and misunderstand, and also found the quiet darkness of my room preference to anything.
i also was discouraged from talking complaining or any other manner of speaking about my situation. i began tx w/o support from this forum (though reading prior to beginning tx, i joined the forum at about 3 mths in. i really needed the kind of understanding that can only be obtained from others in the same situation. i thought about therapy, but i don't think my energy levels could have taken on another obligation.
sunspot - that was a wonder post. thank you for sharing it. i would like to print that one out. despite the fact i a 5 wks post tx - the way i feel on any given day is still so unpredictable. just like your post.
thank you all for being here.
i also was discouraged from talking complaining or any other manner of speaking about my situation. i began tx w/o support from this forum (though reading prior to beginning tx, i joined the forum at about 3 mths in. i really needed the kind of understanding that can only be obtained from others in the same situation. i thought about therapy, but i don't think my energy levels could have taken on another obligation.
sunspot - that was a wonder post. thank you for sharing it. i would like to print that one out. despite the fact i a 5 wks post tx - the way i feel on any given day is still so unpredictable. just like your post.
thank you all for being here.
All you oldtimers may have seen this before but it's been over a year and has bearing on this thread. So here goes again.
Having Hepatitis means many things change, and a lot of them are invisible. Unlike having cancer or being hurt in an accident, most people do not understand even a little about HCV and its effects, and of those that think they know, many are actually mis-informed.
In the spirit of informing those who wish to understand ... These are the things that I would like you to understand about me before you judge me...
Please understand that being sick doesn't mean I'm not still a human being. I have to spend most of my day in considerable pain and exhaustion, and if you visit I probably don't seem like much fun to be with, but I'm still me stuck inside this body. I still worry about life and work and my family and friends, and most of the time I'd still like to hear you talk about yours too.
Please understand the difference between "happy" and "healthy". When you've got the flu you probably feel miserable with it, but I've been sick for years. I can't be miserable all the time, in fact I work hard at not being miserable. So if you're talking to me and I sound happy, it means I'm happy. That's all. It doesn't mean that I'm not in a lot of pain, or extremely tired, or that I'm getting better, or any of those things. Please, don't say, "Oh, you're sounding better!". I am not sounding better, I am sounding happy. If you want to comment on that, you're welcome.
Please understand that being able to stand up for ten minutes, doesn't necessarily mean that I can stand up for twenty minutes, or an hour. And, just because I managed to stand up for thirty minutes yesterday doesn't mean that I can do the same today. With a lot of diseases you're either paralyzed, or you can move. With this one it gets more confusing. Please repeat the above paragraph substituting, "sitting", "walking", "thinking", "being sociable" and so on ... it applies to everything. That's what Hepatitis does to you.
Please understand that HCV or HBV is variable. It's quite possible (for me, it's common) that one day I am able to walk to the park and back, while the next day I'll have trouble getting to the kitchen. Please don't attack me when I'm ill by saying, "But you did it before!", if you want me to do something then ask if I can. In a similar vein, I may need to cancel an invitation at the last minute, if this happens please do not take it personally. Please understand that "getting out and doing things" does not make me feel better. Telling me that I need a treadmill, or that I just need to loose (or gain)weight, get this exercise machine, join this gym, try these classes... may frustrate me to tears, and is not correct... if I was capable of doing these things, don't you know that I would? I am working with my doctor and physical therapist and am already doing the excercise and diet that I am suppose to do. Another statement that hurts is, "You just need to push yourself more, exercise harder..." Obviously HCV deals directly with muscles, and because our muscles don't repair themselves the way your muscles do, this does far more damage than good and could result in recovery time in days or weeks or months from a single activity.
Also, Hepatitis may cause condary depression (wouldn't you get depressed if you were hurting and exhausted for years on end!?) but it is not created by depression. Please understand that if I say I have to sit down/lie down/take these pills now, that I do have to do it right now - it can't be put off or forgotten just because I'm out for the day (or whatever). Hepatitis does not forgive.
If you want to suggest a cure to me, don't. It's not because I don't appreciate the thought, and it's not because I don't want to get well. It's because I have had almost every single one of my friends suggest one at one point or another. At first I tried them all, but then I realized that I was using up so much energy trying things that I was making myself sicker, not better. If there was something that cured, or even helped, all people with hepaititis then we'd know about it. This is not a drug-company conspiracy, there is worldwide networking (both on and off the Internet) between people with Hepatitis if something worked we would KNOW. If after reading that, you still want to suggest a cure, then do it, but don't expect me to rush out and try it. I'll take what you said and discuss it with my doctor.
In many ways I depend on you - people who are not sick - I need you to visit me when I am too sick to go out... Sometimes I need you help me with the shopping, cooking or cleaning. I may need you to take me to the doctor, or to the physical therapist. I need you on a different level too ... you're my link to the outsideworld... if you don't come to visit me, then I might not get to see you... and, as much as it's possible, I need you to understand me.
Authored by Bek Oberin
Having Hepatitis means many things change, and a lot of them are invisible. Unlike having cancer or being hurt in an accident, most people do not understand even a little about HCV and its effects, and of those that think they know, many are actually mis-informed.
In the spirit of informing those who wish to understand ... These are the things that I would like you to understand about me before you judge me...
Please understand that being sick doesn't mean I'm not still a human being. I have to spend most of my day in considerable pain and exhaustion, and if you visit I probably don't seem like much fun to be with, but I'm still me stuck inside this body. I still worry about life and work and my family and friends, and most of the time I'd still like to hear you talk about yours too.
Please understand the difference between "happy" and "healthy". When you've got the flu you probably feel miserable with it, but I've been sick for years. I can't be miserable all the time, in fact I work hard at not being miserable. So if you're talking to me and I sound happy, it means I'm happy. That's all. It doesn't mean that I'm not in a lot of pain, or extremely tired, or that I'm getting better, or any of those things. Please, don't say, "Oh, you're sounding better!". I am not sounding better, I am sounding happy. If you want to comment on that, you're welcome.
Please understand that being able to stand up for ten minutes, doesn't necessarily mean that I can stand up for twenty minutes, or an hour. And, just because I managed to stand up for thirty minutes yesterday doesn't mean that I can do the same today. With a lot of diseases you're either paralyzed, or you can move. With this one it gets more confusing. Please repeat the above paragraph substituting, "sitting", "walking", "thinking", "being sociable" and so on ... it applies to everything. That's what Hepatitis does to you.
Please understand that HCV or HBV is variable. It's quite possible (for me, it's common) that one day I am able to walk to the park and back, while the next day I'll have trouble getting to the kitchen. Please don't attack me when I'm ill by saying, "But you did it before!", if you want me to do something then ask if I can. In a similar vein, I may need to cancel an invitation at the last minute, if this happens please do not take it personally. Please understand that "getting out and doing things" does not make me feel better. Telling me that I need a treadmill, or that I just need to loose (or gain)weight, get this exercise machine, join this gym, try these classes... may frustrate me to tears, and is not correct... if I was capable of doing these things, don't you know that I would? I am working with my doctor and physical therapist and am already doing the excercise and diet that I am suppose to do. Another statement that hurts is, "You just need to push yourself more, exercise harder..." Obviously HCV deals directly with muscles, and because our muscles don't repair themselves the way your muscles do, this does far more damage than good and could result in recovery time in days or weeks or months from a single activity.
Also, Hepatitis may cause condary depression (wouldn't you get depressed if you were hurting and exhausted for years on end!?) but it is not created by depression. Please understand that if I say I have to sit down/lie down/take these pills now, that I do have to do it right now - it can't be put off or forgotten just because I'm out for the day (or whatever). Hepatitis does not forgive.
If you want to suggest a cure to me, don't. It's not because I don't appreciate the thought, and it's not because I don't want to get well. It's because I have had almost every single one of my friends suggest one at one point or another. At first I tried them all, but then I realized that I was using up so much energy trying things that I was making myself sicker, not better. If there was something that cured, or even helped, all people with hepaititis then we'd know about it. This is not a drug-company conspiracy, there is worldwide networking (both on and off the Internet) between people with Hepatitis if something worked we would KNOW. If after reading that, you still want to suggest a cure, then do it, but don't expect me to rush out and try it. I'll take what you said and discuss it with my doctor.
In many ways I depend on you - people who are not sick - I need you to visit me when I am too sick to go out... Sometimes I need you help me with the shopping, cooking or cleaning. I may need you to take me to the doctor, or to the physical therapist. I need you on a different level too ... you're my link to the outsideworld... if you don't come to visit me, then I might not get to see you... and, as much as it's possible, I need you to understand me.
Authored by Bek Oberin
hi mike - ditto to what everyone said... when i told people i was going to re-treat, there was a variety of responses. i have learned to share only with people who i feel are "positive" about my situation. i have several close friends i can talk to, a few people at work, and fortunatly a supportive husband and sons'. i don't answer my phone much - cause i don't want to keep being asked "how are you feeling?" - i let the machine get it and then return calls when i feel up to it. luckily my friends understand - they know when i don't want to talk and they respect that. the tricky part of this whole treatment thing is - that for the most part, most of us look good - the other day i stopped in to work and my boss said "you look fabulous!" - i jokingly said "well, too bad my insides don't feel as good as my outsides look!", with that, he gave me a hug. so, my suggestion would be - find a few people you feel comfortable with, who fully understand what you're going thru, and reach out to tham when you can. you're not alone in your feelings.
peace & blessings,
w.c. missy
peace & blessings,
w.c. missy
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