Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 In a message dated 5/11/00 4:57:21 PM Eastern Daylight Time, belinda@... writes: He simply doesn't care. It's all he can do to go to work and come home 3 days a week (he's still not going in on the day after shots yet.) **** I`m amazed that he is able to work at all. The treatment is extremely difficult. The poor guy deserves KUDOS IMHO........ bless both of you, debmc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Sheila & Belinda: I feel for you so. I would hate to be coping with a sick spouse AND child rearing (which must totally fall on you) AND financial/legal woes. My husband hasn't worked for over 3 yrs (his business went belly up--that's a whole other story for an AA support group). I'm feeling very fortunate right now that I can support us. I guess the only thought I can offer is " first things first. " Got to get them well so they can get back to work. Belinda, could you get power of attorney so that you can keep up with some of the legal stuff that can't be postponed? Do either of you have family you could call on for help? I wish I could help. Tree Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 In a message dated 5/11/00 5:51:33 PM Eastern Daylight Time, quinlyn1@... writes: This must be such an awful treatment for them to have to go through. ***** A friend of mine described it well, the other day..he explained that interferron is akin to the substance your body emits, in order to fight the flu....the stuff, that makes you sick, is NOT the flu, but the interferron.........and the treatment, when given the combo is ½ interferron.......so if you can imagine injecting yourself 3 X weekly, with your worst case of the FLU...that is what we go through..... I am frightened at how my family feels, too....... I know this is hard on you guys, the family members, but remember, we`re scared AND sick, too. And without the treatment, we might be scared, sick AND dead...... There ought to be support group for families of HCV people........you ought to have a good place to vent, i`m certain it`s hard..... Love and health to all, debmc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Belinda, When my husband was on the combo he went to work but was done in by the time he got home. It pretty much meant that after he got home he ate his dinner took his meds and went to bed. He tried to get as much rest as possible on the weekends. Then at some point he started feeling better and actually felt like doing things. This probably isn't very helpful but just try to hang in there and hopefully he will start feeling somewhat better. I do remember at one point early on we pretty much decided that we just needed to lower our standards and so we decided that as long as both of us were still alive and we were still together then it was okay and we could get through it. I'm sorry I wasn't more help, right now I'm wondering why I started this? Carol advice? > > Okay, this probably seems trivial but I need some advice. My husband is > doing okay, not great but not awful on the combo. Of course he's tired and > feeling icky most of the time, and he's become completely apathetic about > EVERYTHING. Unfortunately, we've got some rather severe financial and legal > problems (stemming from me being on prolonged bedrest and unable to work > during my pregnancy) plus he's executor of his dad's estate, which is mired > in debt not to mention the house burned and needs a great deal of clean up > or the city is going to hit the estate with citations, etc. He simply > doesn't care. It's all he can do to go to work and come home 3 days a week > (he's still not going in on the day after shots yet.) I sympathize, but > we're looking at some serious consequences if we don't cope with some of > this stuff, much of which I can't handle because it's legal stuff in his > name. Plus a 4yo, 4 month old and some frantic freelance work to try to > make up for some of the financial stuff tends to limit my time, too. He > gets furious if I ask what we're going to do -- we already have to move, > and how I'm supposed to do that with him in his current condition is beyond > me. Those of you with spouses going through this -- any insight? Is this > just going to be the rest of my life? > > Belinda > > ------------------------------------------------------------------------ > There's still time to order Calyx & Corolla flowers for mom. > These fresh and elegant bouquets are available for delivery > by Mother's Day. To order, please visit > 1/4103/10/_/96144/_/958078586/ > ------------------------------------------------------------------------ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Belinda, I'm sorry that your life is in such chaos right now. You sure do have more on your plate that any one person should. However, your hubby's behavior is not unexpected. I hope the doctors warned you that there was a VERY high possibility of depression with the combo therapy. The literature that we were given when Pat started the treatments said that we could and should expect depression - ranging from mild to suicidal. Unfortunately it's just one more thing that you have to be aware of and keep your eyes open for. You might want to talk to his doctor. I will keep you in my prayers and hope that things get better for you. Jeanie --- Belinda Sawyer <belinda@...> wrote: > > Okay, this probably seems trivial but I need some > advice. My husband is > doing okay, not great but not awful on the combo. Of > course he's tired and > feeling icky most of the time, and he's become > completely apathetic about > EVERYTHING. Unfortunately, we've got some rather > severe financial and legal > problems (stemming from me being on prolonged > bedrest and unable to work > during my pregnancy) plus he's executor of his dad's > estate, which is mired > in debt not to mention the house burned and needs a > great deal of clean up > or the city is going to hit the estate with > citations, etc. He simply > doesn't care. It's all he can do to go to work and > come home 3 days a week > (he's still not going in on the day after shots > yet.) I sympathize, but > we're looking at some serious consequences if we > don't cope with some of > this stuff, much of which I can't handle because > it's legal stuff in his > name. Plus a 4yo, 4 month old and some frantic > freelance work to try to > make up for some of the financial stuff tends to > limit my time, too. He > gets furious if I ask what we're going to do -- we > already have to move, > and how I'm supposed to do that with him in his > current condition is beyond > me. Those of you with spouses going through this -- > any insight? Is this > just going to be the rest of my life? > > Belinda > > ------------------------------------------------------------------------ > There's still time to order Calyx & Corolla flowers > for mom. > These fresh and elegant bouquets are available for > delivery > by Mother's Day. To order, please visit > 1/4103/10/_/96144/_/958078586/ > ------------------------------------------------------------------------ > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Hi Belinda, I'm not going to be much help either,but feel like I am going through the same thing! My husband took hist first treatment last night.Was awake most of the night,shakes,shivering etc.He was suppose to work tonight,tomorrow,off Saturday & then work Sunday thru Thursday.Guess all of this was too overwhelming for hime this morning.He went into work(they had no idea he had been sick before this morning)He explained everything to them & took a leave of absence.Then stayed in bed all day. Now I'm wondering ok,where do we go from here...... Where will the loss of money come from,I've already been carrying the household load the last few months(he use to do SOOO much with the house & kids) Also wondering how long will this go on. Like I said not much help,but feel free to email me. Maybe we can support each other...... Sheila advice? Okay, this probably seems trivial but I need some advice. My husband isdoing okay, not great but not awful on the combo. Of course he's tired andfeeling icky most of the time, and he's become completely apathetic aboutEVERYTHING. Unfortunately, we've got some rather severe financial and legalproblems (stemming from me being on prolonged bedrest and unable to workduring my pregnancy) plus he's executor of his dad's estate, which is miredin debt not to mention the house burned and needs a great deal of clean upor the city is going to hit the estate with citations, etc. He simplydoesn't care. It's all he can do to go to work and come home 3 days a week(he's still not going in on the day after shots yet.) I sympathize, butwe're looking at some serious consequences if we don't cope with some ofthis stuff, much of which I can't handle because it's legal stuff in hisname. Plus a 4yo, 4 month old and some frantic freelance work to try tomake up for some of the financial stuff tends to limit my time, too. Hegets furious if I ask what we're going to do -- we already have to move,and how I'm supposed to do that with him in his current condition is beyondme. Those of you with spouses going through this -- any insight? Is thisjust going to be the rest of my life? Belinda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Hi Sheila, I wish I could say something to help both you and Belinda. You are going through such hard times right now. At least Pat was still able to work while on the treatment, even though he became such an SOB that I wasn't sure if I was going to kill him or if one of our clients was going to beat me to it. This must be such an awful treatment for them to have to go through. Have either of you tried to get social security benefits? I've heard that it is very difficult, but worth a try if they can help with some income. Keep writing. We are all here to help even if all we can do is listen and offer support. My heart breaks for you and your hubbies. Jeanie --- mrsam@... wrote: > Hi Belinda, > I'm not going to be much help either,but feel like > I am going through the same thing! > My husband took hist first treatment last night.Was > awake most of the night,shakes,shivering etc.He was > suppose to work tonight,tomorrow,off Saturday & then > work Sunday thru Thursday.Guess all of this was too > overwhelming for hime this morning.He went into > work(they had no idea he had been sick before this > morning)He explained everything to them & took a > leave of absence.Then stayed in bed all day. > Now I'm wondering ok,where do we go from here...... > Where will the loss of money come from,I've already > been carrying the household load the last few > months(he use to do SOOO much with the house & kids) > Also wondering how long will this go on. > Like I said not much help,but feel free to email > me. > Maybe we can support each other...... > Sheila > advice? > > > > Okay, this probably seems trivial but I need some > advice. My husband is > doing okay, not great but not awful on the combo. > Of course he's tired and > feeling icky most of the time, and he's become > completely apathetic about > EVERYTHING. Unfortunately, we've got some rather > severe financial and legal > problems (stemming from me being on prolonged > bedrest and unable to work > during my pregnancy) plus he's executor of his > dad's estate, which is mired > in debt not to mention the house burned and needs > a great deal of clean up > or the city is going to hit the estate with > citations, etc. He simply > doesn't care. It's all he can do to go to work and > come home 3 days a week > (he's still not going in on the day after shots > yet.) I sympathize, but > we're looking at some serious consequences if we > don't cope with some of > this stuff, much of which I can't handle because > it's legal stuff in his > name. Plus a 4yo, 4 month old and some frantic > freelance work to try to > make up for some of the financial stuff tends to > limit my time, too. He > gets furious if I ask what we're going to do -- we > already have to move, > and how I'm supposed to do that with him in his > current condition is beyond > me. Those of you with spouses going through this > -- any insight? Is this > just going to be the rest of my life? > > Belinda > > ------------------------------------------------------------------------------ > > > > ------------------------------------------------------------------------------ > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Belinda-No this is not going to be the " way it is " for the rest of your life or his either. But it is life right now and you have to take it one day at a time. It is very frustrationg being on the combo and not being able to stay on top of things. That he's even working 3 days is very good. Don't waste your health and energy trying to save or make money because in the long run you'll probably spend lots more money trying to buy your health back. I hear your frustration-but it is only for a season. Let the house go (his fathers) if neither of you can handle it. Write it off. I've had to look at life and visualize worst case senerios and then decide again. Is this what I'm willing to let happen. Not meaning to be gruesome but life is short and when one of you is gone will it all be worth it. Spend every day as if its your last one together. Enjoy each other now and don't sweat the things that won't make any difference in a year or so. Thats my advice. I know exactly where both of you are. We have had those arguments and have come to this conclusion-at least we have each other and the love between us bridges any difficulties we face. At least we can face them together. God Bless you and your husband, Bob Simons Sr. Commander Royal Rangers Tucson, Az. http://abbacomputers.homepage.com/bob.htm For the message of the cross is foolishness to those who are perishing, but to us who are being saved it is the power of God. 1 Cor 1:18 (NKJ) advice? > > Okay, this probably seems trivial but I need some advice. My husband is > doing okay, not great but not awful on the combo. Of course he's tired and > feeling icky most of the time, and he's become completely apathetic about > EVERYTHING. Unfortunately, we've got some rather severe financial and legal > problems (stemming from me being on prolonged bedrest and unable to work > during my pregnancy) plus he's executor of his dad's estate, which is mired > in debt not to mention the house burned and needs a great deal of clean up > or the city is going to hit the estate with citations, etc. He simply > doesn't care. It's all he can do to go to work and come home 3 days a week > (he's still not going in on the day after shots yet.) I sympathize, but > we're looking at some serious consequences if we don't cope with some of > this stuff, much of which I can't handle because it's legal stuff in his > name. Plus a 4yo, 4 month old and some frantic freelance work to try to > make up for some of the financial stuff tends to limit my time, too. He > gets furious if I ask what we're going to do -- we already have to move, > and how I'm supposed to do that with him in his current condition is beyond > me. Those of you with spouses going through this -- any insight? Is this > just going to be the rest of my life? > > Belinda > > ------------------------------------------------------------------------ > There's still time to order Calyx & Corolla flowers for mom. > These fresh and elegant bouquets are available for delivery > by Mother's Day. To order, please visit > 1/4103/10/_/96144/_/958078586/ > ------------------------------------------------------------------------ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 A friend of mine who knows what I'm going through says " theres not many options for you considering that the disease is terminal! " We need to keep that in mind. Since being on this medication I have been so frustrated because of my lack of energy and emotional ups and downs (mostly down) and loss of memory. It is not easy dealing with all that alone let alone the pain and aches I have almost constantly. My attitude and mouth has gotten me in more trouble (saying things without thinking) and have had to apologize to my wife and kids more than once. One night this week I went and sat in dry river bed a few block from house and tried to put the pieces together, after fighting with my wife. I felt like a heel and sent her a bouquet of flowers the next day with a note saying I was sorry. I'm anemic, and am susceptible to infections. Have been in the hosp. for a surgical procedure to open up a abcess. I sleep almost all day now 10-12hrs per day. If I get up sooner (which I've tried ) I feel like crap all day and am even more irritable and don't feel like doing anything. At least with plenty of sleep I will do some cleaning and make dinner and can make through the day without forgetting to take some pills or something else like fighting with my wife. I only have 3 more months of treatment left and we are counting the days. I'm hopeful that the virus will stay away and that is what keeps driving us on. Hang in there is all can say and keep looking on the positive side of things. One good thing is the mesquitos don't bite me cause they apparently don't like the meds in my blood. Also I missed getting that bad flu that ran around so there are things to be thankful for. your friend, Bob Simons Sr. Commander Royal Rangers Tucson, Az. http://abbacomputers.homepage.com/bob.htm For the message of the cross is foolishness to those who are perishing, but to us who are being saved it is the power of God. 1 Cor 1:18 (NKJ) Re: advice? In a message dated 5/11/00 5:51:33 PM Eastern Daylight Time, quinlyn1@... writes: This must be such an awful treatment for them to have to go through. ***** A friend of mine described it well, the other day..he explained that interferron is akin to the substance your body emits, in order to fight the flu....the stuff, that makes you sick, is NOT the flu, but the interferron.........and the treatment, when given the combo is ½ interferron.......so if you can imagine injecting yourself 3 X weekly, with your worst case of the FLU...that is what we go through..... I am frightened at how my family feels, too....... I know this is hard on you guys, the family members, but remember, we`re scared AND sick, too. And without the treatment, we might be scared, sick AND dead...... There ought to be support group for families of HCV people........you ought to have a good place to vent, i`m certain it`s hard..... Love and health to all, debmc ------------------------------------------------------------------------ There's still time to order Calyx & Corolla flowers for mom. These fresh and elegant bouquets are available for delivery by Mother's Day. To order, please visit 1/4103/10/_/96144/_/958086901/ ------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 At 07:14 PM 5/11/2000 -0400, you wrote: >The poor guy deserves KUDOS IMHO........ and >There ought to be support group for families of HCV people........you ought >to have a good place to vent, i`m certain it`s hard..... >Love and health to all, >debmc I thought this was a support group for families and HCV people. A lot of the people who post to this list seem to be family members, collecting insight and information for a loved one who's just too tired and out of sorts to do it themselves. Don't get me wrong, please. I am not belittling what you, my husband or any other HCV patient goes through. I know I'm whining and it seems really self-indulgent since I'm not even sick. Part of my frustration is seeing my husband, whom I love more than life, change from someone so vital, full of fun and life, to this shadow of himself. Nothing I'm facing comes close to what he and many of you are going through. I know it's taking all he's got to get from day to day. That leaves me to take over the big picture for our family. It's just that our big picture right now includes foreclosure, bankruptcy, a forced move, additional legal issues connected with my fil's estate, a 4yo who is suddenly sleepwalking with night terrors, a 4 month old premie with her own set of medical issues and 3 clients who are demanding to know why the hell I can't meet a deadline anymore. I'm just a little overwhelmed. I'm venting to you guys because most of our off-line friends don't know the extent of what we're facing and were already seeming a bit overloaded hearing about the baby's problems BEFORE we found out about 's hepC. I'm not sure they could handle the litany I just shared with you, but I know individuals in this group have faced worse troubles with grace, humor and an understanding of what's really important so I figured it was safe. I really appreciate your kind support, and hope I can return the favor sometime. thanks to all-- Belinda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Belinda, Please feel free to vent anytime you need to. You're right, that's what we are here for. We can't do a whole lot, but we can sure listen and offer suggestion and support. You go right ahead and whine if you need to right now. Jeanie --- Belinda Sawyer <belinda@...> wrote: > At 07:14 PM 5/11/2000 -0400, you wrote: > > >The poor guy deserves KUDOS IMHO........ > and > >There ought to be support group for families of > HCV people........you ought > >to have a good place to vent, i`m certain it`s > hard..... > >Love and health to all, > >debmc > > I thought this was a support group for families and > HCV people. A lot of > the people who post to this list seem to be family > members, collecting > insight and information for a loved one who's just > too tired and out of > sorts to do it themselves. > > Don't get me wrong, please. I am not belittling what > you, my husband or any > other HCV patient goes through. I know I'm whining > and it seems really > self-indulgent since I'm not even sick. Part of my > frustration is seeing my > husband, whom I love more than life, change from > someone so vital, full of > fun and life, to this shadow of himself. Nothing I'm > facing comes close to > what he and many of you are going through. I know > it's taking all he's got > to get from day to day. > > That leaves me to take over the big picture for our > family. It's just that > our big picture right now includes foreclosure, > bankruptcy, a forced move, > additional legal issues connected with my fil's > estate, a 4yo who is > suddenly sleepwalking with night terrors, a 4 month > old premie with her own > set of medical issues and 3 clients who are > demanding to know why the hell > I can't meet a deadline anymore. I'm just a little > overwhelmed. I'm venting > to you guys because most of our off-line friends > don't know the extent of > what we're facing and were already seeming a bit > overloaded hearing about > the baby's problems BEFORE we found out about > 's hepC. I'm not sure > they could handle the litany I just shared with you, > but I know individuals > in this group have faced worse troubles with grace, > humor and an > understanding of what's really important so I > figured it was safe. I really > appreciate your kind support, and hope I can return > the favor sometime. > > thanks to all-- > Belinda > > ------------------------------------------------------------------------ > Remember four years of good friends, bad clothes, > explosive chemistry > experiments. > 1/4051/10/_/96144/_/958096466/ > ------------------------------------------------------------------------ > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 Dear Bob and Deb, Thank you for giving us, the family members, your perspective. Sometimes we get so caught up with what we are going through that we need to be reminded that you too are scared and tired of the side effects of the treatments. Thank you for the reminders. Jeanie --- Bob Simons <bsimons@...> wrote: > A friend of mine who knows what I'm going through > says " theres not many > options for you considering that the disease is > terminal! " > We need to keep that in mind. > Since being on this medication I have been so > frustrated because of my lack > of energy and emotional ups and downs (mostly down) > and loss of memory. It > is not easy dealing with all that alone let alone > the pain and aches I have > almost constantly. My attitude and mouth has gotten > me in more trouble > (saying things without thinking) and have had to > apologize to my wife and > kids more than once. One night this week I went and > sat in dry river bed a > few block from house and tried to put the pieces > together, after fighting > with my wife. > I felt like a heel and sent her a bouquet of flowers > the next day with a > note saying I was sorry. > I'm anemic, and am susceptible to infections. Have > been in the hosp. for a > surgical procedure to open up a abcess. > I sleep almost all day now 10-12hrs per day. If I > get up sooner (which I've > tried ) I feel like crap all day and am even more > irritable and don't feel > like doing anything. At least with plenty of sleep I > will do some cleaning > and make dinner and can make through the day without > forgetting to take some > pills or something else like fighting with my wife. > I only have 3 more months of treatment left and we > are counting the days. > I'm hopeful that the virus will stay away and that > is what keeps driving us > on. > Hang in there is all can say and keep looking on the > positive side of > things. One good thing is the mesquitos don't bite > me cause they apparently > don't like the meds in my blood. Also I missed > getting that bad flu that ran > around so there are things to be thankful for. > your friend, > Bob Simons > Sr. Commander > Royal Rangers > Tucson, Az. > http://abbacomputers.homepage.com/bob.htm > For the message of the cross is foolishness > to those who are perishing, but to us who > are being saved it is the power of God. > 1 Cor 1:18 (NKJ) > Re: advice? > > > In a message dated 5/11/00 5:51:33 PM Eastern > Daylight Time, > quinlyn1@... writes: > This must be such an awful treatment for them to > have to go through. > ***** > A friend of mine described it well, the other > day..he explained that > interferron is akin to the substance your body > emits, in order to fight the > flu....the stuff, that makes you sick, is NOT the > flu, but the > interferron.........and the treatment, when given > the combo is ½ > interferron.......so if you can imagine injecting > yourself 3 X weekly, with > your worst case of the FLU...that is what we go > through..... > I am frightened at how my family feels, too....... > I know this is hard on you guys, the family members, > but remember, we`re > scared AND sick, too. And without the treatment, we > might be scared, sick > AND > dead...... > There ought to be support group for families of HCV > people........you ought > to have a good place to vent, i`m certain it`s > hard..... > Love and health to all, > debmc > > ------------------------------------------------------------------------ > There's still time to order Calyx & Corolla flowers > for mom. > These fresh and elegant bouquets are available for > delivery > by Mother's Day. To order, please visit > 1/4103/10/_/96144/_/958086901/ > ------------------------------------------------------------------------ > > > > > > ------------------------------------------------------------------------ > There's still time to order Calyx & Corolla flowers > for mom. > These fresh and elegant bouquets are available for > delivery > by Mother's Day. To order, please visit > 1/4103/10/_/96144/_/958093778/ > ------------------------------------------------------------------------ > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2000 Report Share Posted May 11, 2000 thank you for all the messages of support we give each other. It is so nice to see the perspective of being on the shots as well as being on the other side. I am still on 9 medications at this point from having only 2 shots. My lungs are just not gettting better. I definitely understand the worry of other family issues. My daughter has special needs and that just by itself can become overwhelming. Is there a chance you would qualify for respite for her? That could give you the break to work on some of your other pressing matters. Respite will often take care of siblings also. I can tell you how to check into it. I am not sure what state you are in. It is possible that a pro bono lawyer or maybe someone with like AARP could help you draft a letter or have someone appointed as a conservator over the dad's estate or possibly give you some extra time with a letter explaining your circumstances. Do you have a church group or friends that could possibly bring you dinner a couple of nights a week or may be willing to come to the house to watch the children while you work on deadlines? COuld you possibly change the children's bedtime or naptime schedule to help you with your work? I dont pretend to have easy answers. Just attempting brainstorming to see what you think. Debra angel in Alaska Re: advice? > > > > > > In a message dated 5/11/00 5:51:33 PM Eastern > > Daylight Time, > > quinlyn1@... writes: > > This must be such an awful treatment for them to > > have to go through. > > ***** > > A friend of mine described it well, the other > > day..he explained that > > interferron is akin to the substance your body > > emits, in order to fight the > > flu....the stuff, that makes you sick, is NOT the > > flu, but the > > interferron.........and the treatment, when given > > the combo is ½ > > interferron.......so if you can imagine injecting > > yourself 3 X weekly, with > > your worst case of the FLU...that is what we go > > through..... > > I am frightened at how my family feels, too....... > > I know this is hard on you guys, the family members, > > but remember, we`re > > scared AND sick, too. And without the treatment, we > > might be scared, sick > > AND > > dead...... > > There ought to be support group for families of HCV > > people........you ought > > to have a good place to vent, i`m certain it`s > > hard..... > > Love and health to all, > > debmc > > > > > ------------------------------------------------------------------------ > > There's still time to order Calyx & Corolla flowers > > for mom. > > These fresh and elegant bouquets are available for > > delivery > > by Mother's Day. To order, please visit > > > 1/4103/10/_/96144/_/958086901/ > > > ------------------------------------------------------------------------ > > > > > > > > > > > > > ------------------------------------------------------------------------ > > There's still time to order Calyx & Corolla flowers > > for mom. > > These fresh and elegant bouquets are available for > > delivery > > by Mother's Day. To order, please visit > > > 1/4103/10/_/96144/_/958093778/ > > > ------------------------------------------------------------------------ > > > > > > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 Bob: Everytime I feel sorry for myself because everything falls on me and we're just existing here, I realize he's feeling far worse than I do. Remarkably, even though he feels like crap and his back hurts all the time, he is never mean with me or anyone else (of course he hasn't taken the meds either). I can be grouchy with far less provocation, so I can imagine what I would be like! I'm sure the flowers went a long way with your wife (we just love them). Three more months--just think, by August you'll be a new man! We're all rooting for you. Tree Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 Belinda: You are right that most people " on the outside " cannot comprehend what Hep C does to a family. They just don't get it. My husband may pull it together and go with me to a family dinner, and they'll say to me, " well he looks okay to me " (what, I'm lying?) What they don't realize is he slept until we left the house and then fell back to sleep in the car on the way home. I know you're going to think " with all I have to think about, you ask me this? " but is there any way you can get some relief for yourself, like counseling? After all, with everyone depending on you right now, you all can't afford for you to have a melt down. Any churches in your area offer any of that type of support (for free)? Tree Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 Belinda-I guess we're all sidewalk philosophers when it comes to advice. I try to speak from heart and I know we are trying to be honest and help you as much as we can. No one said it was gonna be easy, but if we take it one day at a time, it's the only way I've been able to cope with it. My wife was diagnosed with breast cancer about the same time I was diagnosed with HCV. We found that we could do very little about it. I tried to be there all the time for my wife. If anything, we have stepped back and taken a long hard look life and realized that some things just didn't matter. We became a lot closer as we cared for each other and in that respect we have been blessed. Life goes on and we can make it more difficult by allowing outside pressure to interfere. Some friends tried to help us by advising us about all different medicines-natural, herbal, etc. We listened but realized that if we tried everything we would be out of money and have no time for anything. I knew I had to get my wife through surgery and chemo and radiation and everything else came second if it came at all. Without her I wouldn't know where to go anyway. We did get a lot of support from friends at our church-a whole lot and we didn't feel under pressure to have to repay anyone for their acts of kindness. We have done it for it for others and know that's part of the deal. Many years ago I watched a good friend die from cancer and he was a great influence to me at that time. Even in his last days he always smiled (even though he was on so much pain meds.) as he tried to help others in his ward. He would try to cheer them up and would talk to them about God. He would pray with them if they let him. The nurses there all loved him. He made their job easy. And now I say thats the way I want to remembered when I go. Not feeling sorry for myself (like I do alot) but trying to cheer others up. I hope I don't sound like I'm coming down on you-I'm just trying to relate where I am and what has helped me. My wife means a lot to me and I would give the world to be able to stay by her side. No amount of money will buy my love for her. So tell the clients why you can't meet deadlines anymore and if they're any kind of decend humans they'll give you more time and if not than you don't need to do business with them. I've run 2 businesses and my family and my health came first. My customers understood because I made them understand-if they wanted someone honest who loves his family, to do business with, than they would have to take a back seat to what are my priorities. Yes, I lost some customers who wanted things right now, but in the end I had customers who I came to know and be friends with also. I sit back now and let my sons run the business. I hope and pray that they learn the same priorities and principles that I did. I'll pray that this helps and that you can find some answers to your questions through all of this. Bob Simons Sr. Commander Royal Rangers Tucson, Az. http://abbacomputers.homepage.com/bob.htm For the message of the cross is foolishness to those who are perishing, but to us who are being saved it is the power of God. 1 Cor 1:18 (NKJ) Re: advice? > At 07:14 PM 5/11/2000 -0400, you wrote: > > >The poor guy deserves KUDOS IMHO........ > and > >There ought to be support group for families of HCV people........you ought > >to have a good place to vent, i`m certain it`s hard..... > >Love and health to all, > >debmc > > I thought this was a support group for families and HCV people. A lot of > the people who post to this list seem to be family members, collecting > insight and information for a loved one who's just too tired and out of > sorts to do it themselves. > > Don't get me wrong, please. I am not belittling what you, my husband or any > other HCV patient goes through. I know I'm whining and it seems really > self-indulgent since I'm not even sick. Part of my frustration is seeing my > husband, whom I love more than life, change from someone so vital, full of > fun and life, to this shadow of himself. Nothing I'm facing comes close to > what he and many of you are going through. I know it's taking all he's got > to get from day to day. > > That leaves me to take over the big picture for our family. It's just that > our big picture right now includes foreclosure, bankruptcy, a forced move, > additional legal issues connected with my fil's estate, a 4yo who is > suddenly sleepwalking with night terrors, a 4 month old premie with her own > set of medical issues and 3 clients who are demanding to know why the hell > I can't meet a deadline anymore. I'm just a little overwhelmed. I'm venting > to you guys because most of our off-line friends don't know the extent of > what we're facing and were already seeming a bit overloaded hearing about > the baby's problems BEFORE we found out about 's hepC. I'm not sure > they could handle the litany I just shared with you, but I know individuals > in this group have faced worse troubles with grace, humor and an > understanding of what's really important so I figured it was safe. I really > appreciate your kind support, and hope I can return the favor sometime. > > thanks to all-- > Belinda > > ------------------------------------------------------------------------ > Remember four years of good friends, bad clothes, explosive chemistry > experiments. > 1/4051/10/_/96144/_/958096466/ > ------------------------------------------------------------------------ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 Debra-did you have an Asthma reaction or was it something else? I remember you telling about it but I don't remeber the details. Did you just do the shots and not the Ribivarin caps? The Ribaviran are what give me problems. The Int. shots I did for over 5 months and felt like I could do them for the rest of life (in comparison to the Combo). Everyone has different reactions though. Bob Simons Sr. Commander Royal Rangers Tucson, Az. http://abbacomputers.homepage.com/bob.htm For I know the plans I have for you, " declares the LORD, " plans to prosper you and not to harm you, plans to give you hope and a future.Jer 29:11(NIV) Re: advice? > > > > > > > > > In a message dated 5/11/00 5:51:33 PM Eastern > > > Daylight Time, > > > quinlyn1@... writes: > > > This must be such an awful treatment for them to > > > have to go through. > > > ***** > > > A friend of mine described it well, the other > > > day..he explained that > > > interferron is akin to the substance your body > > > emits, in order to fight the > > > flu....the stuff, that makes you sick, is NOT the > > > flu, but the > > > interferron.........and the treatment, when given > > > the combo is ½ > > > interferron.......so if you can imagine injecting > > > yourself 3 X weekly, with > > > your worst case of the FLU...that is what we go > > > through..... > > > I am frightened at how my family feels, too....... > > > I know this is hard on you guys, the family members, > > > but remember, we`re > > > scared AND sick, too. And without the treatment, we > > > might be scared, sick > > > AND > > > dead...... > > > There ought to be support group for families of HCV > > > people........you ought > > > to have a good place to vent, i`m certain it`s > > > hard..... > > > Love and health to all, > > > debmc > > > > > > > > ------------------------------------------------------------------------ > > > There's still time to order Calyx & Corolla flowers > > > for mom. > > > These fresh and elegant bouquets are available for > > > delivery > > > by Mother's Day. To order, please visit > > > > > 1/4103/10/_/96144/_/958086901/ > > > > > ------------------------------------------------------------------------ > > > > > > > > > > > > > > > > > > > > ------------------------------------------------------------------------ > > > There's still time to order Calyx & Corolla flowers > > > for mom. > > > These fresh and elegant bouquets are available for > > > delivery > > > by Mother's Day. To order, please visit > > > > > 1/4103/10/_/96144/_/958093778/ > > > > > ------------------------------------------------------------------------ > > > > > > > > > > > > __________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 In a message dated 5/11/00 9:55:24 PM Eastern Daylight Time, belinda@... writes: I thought this was a support group for families and HCV people. A lot of the people who post to this list seem to be family members, collecting insight and information for a loved one who's just too tired and out of sorts to do it themselves. ***** My words did not fit my thoughts>>sorry..I meant a group In real life..........like, there are groups for us, to meet and we can open up, cry, vent, act out our anger, loved ones of HCV should enjoy the same thing.........I cannot imagine how hard or crazy-making this is for those of you who don`t have HCV, yet whose lives are seeming to fall apart from it`s effects..... But this list IS for all of us, famililes and patients......and this IS a place to vent. We just went through foreclosure and bankruptcy...thankfully, we were able to hold on to the house, it`s nearly ½ paid for, would have been hard to lose it.....so I know what you are facing. See an attorney, perhaps one can help with some of your burdens, sure helped me. ((we bankrupted the day before the house was to be sold at auction. I opened the door, and a man was there, and he told me he had just paid 121 K for my 200 K house...the mortgage company had not stopped the sale. The sale was recended, but you can imagine what type day THAT was for me. Then to make it worse, he had advertised it to a bunch of people, and we had skads of families driving down our private drive, to look at our house, for days this went on. I`m a dog trainer, and have protection-trained dogs here, so this was NOT a great thing...I was terrifed one of the people would open the gate.....)) Anyway.......I feel for your pain..wish I could be some help. Love and good health to all, debmc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 At 12:18 AM 5/12/2000 -0700, you wrote: >My wife was diagnosed with breast cancer about the same time I was diagnosed >with HCV. We found that we could do very little about it. I tried to be >there all the time for my wife. If anything, we have stepped back and taken >a long hard look life and realized that some things just didn't matter. Bob - thanks for talking so personally. I've respected your attitude and perspective on the list for a long time now, and your responses to my frustration have just reinforced that opinion. I really appreciate your encouragement. How is your wife doing now? with prayers that at the end of treatment your virus is gone gone gone Belinda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 At 08:02 PM 5/11/2000 -0800, you wrote: >thank you for all the messages of support we give each other. It is so nice >to see the perspective of being on the shots as well as being on the other >side. I am still on 9 medications at this point from having only 2 shots. >My lungs are just not gettting better. Debra -- I can't believe you're even checking e-mail, much less trying to help me work out my problems. Has your doctor left yet? Who is taking care of you until the new doc arrives? I'm really praying that your lungs will heal. I can only imagine how frightening this has been for you, particularly with a daughter who needs your care. Thinking of you -- Belinda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 Belinda- Shes doing great. Gets her check up every 6 months and I can tell she gets real antsy about the results. When they come back negative she sighs a big sigh of relief. I don't worry so much about it until I get bad results. I think I'm more practical and not into worrying for no good reason. Most men are like that I think. From what I hear it will take a little longer for the meds to flush my system. Actually 2-6 months after I stop. I'm in a real good support group with folks that are done with it and they come back to let us know how they're doing. We've had a bunch healed for good with the Rebetron so I am enthusiastic. They say it all starts coming back to you-memory, energy, wow! I'm getting giddy! Hang in there. You're not alone. Bob Simons Sr. Commander Royal Rangers Tucson, Az. http://abbacomputers.homepage.com/bob.htm For I know the plans I have for you, " declares the LORD, " plans to prosper you and not to harm you, plans to give you hope and a future. Jer 29:11 (NIV) Re: advice? > At 12:18 AM 5/12/2000 -0700, you wrote: > > >My wife was diagnosed with breast cancer about the same time I was diagnosed > >with HCV. We found that we could do very little about it. I tried to be > >there all the time for my wife. If anything, we have stepped back and taken > >a long hard look life and realized that some things just didn't matter. > > Bob - > thanks for talking so personally. I've respected your attitude and > perspective on the list for a long time now, and your responses to my > frustration have just reinforced that opinion. I really appreciate your > encouragement. > > How is your wife doing now? > > with prayers that at the end of treatment your virus is gone gone gone > Belinda > > ------------------------------------------------------------------------ > Remember four years of good friends, bad clothes, explosive chemistry > experiments. > 1/4051/10/_/96144/_/958128357/ > ------------------------------------------------------------------------ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 Tree, you are so right about how they react when they see your husband. I go through the same thing. He looks fine he~ isn't sick ~you are nuts, etc.... Well, I tell you I have just about had it really. He works and comes home and eats very little and sleeps for a while and then goes to bed what a life!!!!! He cant goon the treatment so I have no idea how that personally affects anyone's life just what we go through and it S***S. I just got out of the hospital from what was thought to be a heart attack, actually stress very bad and now I have to change a few things about the way I. Iive, Well that's easier said than done. I am not tolerant of things anymore and that includes well meaning people who haven't a clue. That's why I came here for I know there are others who are going through the same things. I have to admit some here are a lot stronger than I at times but I do what I can one day at a time. Irish Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 At 08:51 AM 5/12/2000 -0400, you wrote: >***** >My words did not fit my thoughts>>sorry.. No need to say sorry, I was particularly touchy. I was worried I'd offended you -- glad you're still talking to me! >We just went through foreclosure and bankruptcy...thankfully, we were able to >hold on to the house, it`s nearly ½ paid for, would have been hard to lose >it.....so I know what you are facing. aha! so it's not the end of the world. I've been trying to keep " stuff-related " troubles separate from " people-related " troubles but sometimes all the details just make it crazy. We'll actually be glad to get out of the house, it's been a mistake and a money drain since we bought it, plus the area's declined thanks to some nearby rezoning. It's the process that I dread. The scenario you described with all the strangers in your driveway and coming to your door is exactly my recurring nightmare. I've made two appointments with lawyers, then canceled because got mad and said he was handling it, seeing an attorney that day, I need to trust him, etc -- but he hasn't. That's what set me off yesterday, (coupled with the letter about the auction and a nasty note from the IRS.) He can't admit yet that he needs help taking care of the stuff he would normally handle, but he's just so exhausted . . . This too shall pass, and with luck and God's grace he'll respond to this infernal treatment and in 5 years we'll congratulate ourselves on living through this last year of the old millennium. (For those of you who start counting at 2000, forgive me, but I'm holding out for 2001 in the hopes my next century can start on a brighter note!) Thanks for understanding and shedding light for me! Belinda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 yes. there was a really rare side effect of a couple of people that had mild asthma. When they took the interferon it got out of control. THat is what mine has done and I am having a really hard time getting better. I felt better yesterday than I do today. ALl the steroids and stuff amke me feel like a balloon. I did not do the Ribavirin only the interferon. Debra Re: advice? > > > > > > > > > > > > In a message dated 5/11/00 5:51:33 PM Eastern > > > > Daylight Time, > > > > quinlyn1@... writes: > > > > This must be such an awful treatment for them to > > > > have to go through. > > > > ***** > > > > A friend of mine described it well, the other > > > > day..he explained that > > > > interferron is akin to the substance your body > > > > emits, in order to fight the > > > > flu....the stuff, that makes you sick, is NOT the > > > > flu, but the > > > > interferron.........and the treatment, when given > > > > the combo is ½ > > > > interferron.......so if you can imagine injecting > > > > yourself 3 X weekly, with > > > > your worst case of the FLU...that is what we go > > > > through..... > > > > I am frightened at how my family feels, too....... > > > > I know this is hard on you guys, the family members, > > > > but remember, we`re > > > > scared AND sick, too. And without the treatment, we > > > > might be scared, sick > > > > AND > > > > dead...... > > > > There ought to be support group for families of HCV > > > > people........you ought > > > > to have a good place to vent, i`m certain it`s > > > > hard..... > > > > Love and health to all, > > > > debmc > > > > > > > > > > > ------------------------------------------------------------------------ > > > > There's still time to order Calyx & Corolla flowers > > > > for mom. > > > > These fresh and elegant bouquets are available for > > > > delivery > > > > by Mother's Day. To order, please visit > > > > > > > 1/4103/10/_/96144/_/958086901/ > > > > > > > ------------------------------------------------------------------------ > > > > > > > > > > > > > > > > > > > > > > > > > > > ------------------------------------------------------------------------ > > > > There's still time to order Calyx & Corolla flowers > > > > for mom. > > > > These fresh and elegant bouquets are available for > > > > delivery > > > > by Mother's Day. To order, please visit > > > > > > > 1/4103/10/_/96144/_/958093778/ > > > > > > > ------------------------------------------------------------------------ > > > > > > > > > > > > > > > > > __________________________________________________ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 Irish: That's what's so great about this list--everyone understands. Your chest pains were stress related? Your body is trying to tell you something. Please take care of yourself too. Let's join Belinda in looking forward to 2001 for better days! Love you all, Tree Quote Link to comment Share on other sites More sharing options...
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