Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 HOW DID YOU LOSE THE WEIGHT IF YOU DON'T MIND ME ASKING. I HARDLY REALLY EAT ANYTHING AND I GAIN AT LEAST 5 POUNDS A WEEK 'Be kinder than necessary because everyone you meet is fighting some kind of battle. From: Matchinsky <mmatchinsky@ gmail.com> Subject: [HepatitisCSupportG roupForDummies] Introduction To: HepatitisCSupportGr oupForDummies@ yahoogroups. com Date: Thursday, December 11, 2008, 7:13 AM Hi, my name is . I was a member of this group before, but had subscribed to too many groups, and cut this one. I left one of the groups I kept because of a disagreement; a mod was providing false information and insisting it was accurate. My position was and always will be that one should trust their doctor, but if you find you can¢t, then it¢s time to get a new doctor. They¢re only human and they make mistakes but they have the real-world experience (and full background information) to make decisions. Of course, it¢s important to provide that background information. Medicine should make sense, and if it doesn¢t, ask questions or get a second opinion! I am 53 years and married to a wonderfully supportive woman who only happens to be a pediatric nurse. She does look out for me though. She attends all of my appointments, since my memory is at issue. I am also a recovering addict and did anything and everything for 20 years. When I finally went to treatment, I was injecting cocaine, which I am sure is how I contracted this virus. I¢ve been clean and sober for 20 years now. For over 10 years I worked as a substance abuse counselor and went to school, culminating in a Master¢s degree in Addiction Psychology. I¢ve also taught psychology at the local community college. My disease has progressed to Late Stage Liver Disease (LSLD = cirrhosis, but my liver isn¢t in immediate danger of shutting down) and I have developed hepatic y,encephalopath which is doing permanent neurological damage. I can¢t work anymore. My memory is shot, the fog is terrible and I¢m losing my sense of balance, so I walk with a cane. I can walk about a block, maybe two small ones, but that¢s about it. Stairs are a killer. In September I was hospitalized for 5 days due to the encephalopathy. Currently, I am undergoing my third treatment. This time around I am doing Infergen, which is a daily injectable form of interferon. My second treatment was cut short by the insurance company. I was supposed to go 72 weeks, but they stopped it at 52. After several weeks of fighting with them, I was approved for the full 72 weeks. So, I¢ve been on treatment almost 2 years, with only a short break in-between the two treatments. As my hemoglobin tends to drop, I am also on Procrit. I have great doctors, including a hepatologist and internist. I¢ve had trouble with psychiatrists (I have mental health issues as well) but recently the insurance company approved for me to go see the shrink I¢d seen for many years, but had to stop because of insurance (he¢s not in-network). I¢ve applied for SS disability, but was turned down twice. They said that since I had my arms and legs, I couldn¢t be considered disabled! My attorney is appealing this decision, but my understanding is that we are now waiting for a hearing with a judicial judge which could take up to 2 years. Our money will not last much longer, so this is a source of stress as well. Well, I guess that¢s enough for now. Even typing this much wears me out, though I can work a mouse without too much trouble. J Matchinsky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 I know it seems weird, but you HAVE to eat to lose weight. The doctor told me that I was going to need a transplant, that it was inevitable. He said that at my weight, I would not be eligible though. That seems to have motivated me. He has since said that it’s no longer inevitable, considering my weight loss. He places my chances of NOT needing a TP at 80%! I watched calories, fiber and fat. Potion control has been important, too. No more greasy cheeseburgers and fries, unfortunately. No more candy bars or pastries or take-out pizza. The doc wanted me on a 1500 calorie a day diet; I probably am eating 1800 give or take. I also try to have 3 dairy a day, too. (That’s a Weight Watchers thing; my wife is doing WW, but I kinda modified that since I hate counting points..) I’m not fond of raw vegetables, but I eat lots of fruit. I eat breakfast, no sugar cereal w/milk (and sometimes Splenda) or oatmeal, non-fat yogurt and a banana. Then comes a mid-morning snack, usually fruit (apple or no sugar added apple sauce) and a fiber bar. I eat lunch, which varies, but is often low-fat turkey-sausage, egg and cheese sandwich or perhaps a bowl of oatmeal or a frozen entre. Lunch includes fruit, usually grapes. A mid afternoon snack comes next, usually a banana and a 100 calories snack pack of some sort. Dinner includes no sugar added pudding and a no sugar fruit cup. Again, portion control is key, even though single serving packages are a little more expensive. We might have a frozen entre, or Bocca burgers which are a vegetable substitute for burgers, so I still have a taste of cheese burgers. There is also many low-calorie pizzas on the market; they’re thin crusted, and often vegetable, such as mushrooms, olives, or spinach. Never thought I’d like spinach pizza, but it’s good. Fish and chicken and even a little pork are on the menu as well. We also have a low-calorie snack mid-evening. WW makes lots of good deserts, though I prefer something called “Skinny Cow.” I really don’t feel hungry, and at times I hafta force myself to eat. But if a person doesn’t eat, the body goes into starvation mode, and hangs onto fat. The 100 calorie packs are great. There are pastries, including Ho Hos, so I get a taste of chocolate (the pudding helps, too.) 3 little cupcakes, that can be eaten in two bites each, but it’s a taste. I sometimes have those with my morning coffee. We go out to eat weekly. Subway has good stuff. Baked chips with a sandwich . It’s not too hard to find good, healthy food in restaurants. Some have a WW menu, others a smaller portion menu. I’ve had some surprises, though. Rice can be very fattening, though we sometimes have steamed brown rice. Often, we actually have a chocolate chip cookie when we go out! It has surprised me how quickly the weight has come off. I’m also surprised that I do not feel hungry or deprived. Being a recovering addict, I know that food was my first drug of choice, and I know that if I do have cravings, they will soon pass if I don’t pay them much attention. Sorry to have rambled on, but I’m proud of what I’ve done. m From: HepatitisCSupportGroupForDummies [mailto:HepatitisCSupportGroupForDummies ] On Behalf Of Newton Sent: Friday, December 12, 2008 12:07 PM To: HepatitisCSupportGroupForDummies Subject: RE: Introduction HOW DID YOU LOSE THE WEIGHT IF YOU DON'T MIND ME ASKING. I HARDLY REALLY EAT ANYTHING AND I GAIN AT LEAST 5 POUNDS A WEEK 'Be kinder than necessary because everyone you meet is fighting some kind of battle. From: Matchinsky <mmatchinsky@ gmail.com> Subject: [HepatitisCSupportG roupForDummies] Introduction To: HepatitisCSupportGr oupForDummies@ yahoogroups. com Date: Thursday, December 11, 2008, 7:13 AM Hi, my name is . I was a member of this group before, but had subscribed to too many groups, and cut this one. I left one of the groups I kept because of a disagreement; a mod was providing false information and insisting it was accurate. My position was and always will be that one should trust their doctor, but if you find you can¢t, then it¢s time to get a new doctor. They¢re only human and they make mistakes but they have the real-world experience (and full background information) to make decisions. Of course, it¢s important to provide that background information. Medicine should make sense, and if it doesn¢t, ask questions or get a second opinion! I am 53 years and married to a wonderfully supportive woman who only happens to be a pediatric nurse. She does look out for me though. She attends all of my appointments, since my memory is at issue. I am also a recovering addict and did anything and everything for 20 years. When I finally went to treatment, I was injecting cocaine, which I am sure is how I contracted this virus. I¢ve been clean and sober for 20 years now. For over 10 years I worked as a substance abuse counselor and went to school, culminating in a Master¢s degree in Addiction Psychology. I¢ve also taught psychology at the local community college. My disease has progressed to Late Stage Liver Disease (LSLD = cirrhosis, but my liver isn¢t in immediate danger of shutting down) and I have developed hepatic y,encephalopath which is doing permanent neurological damage. I can¢t work anymore. My memory is shot, the fog is terrible and I¢m losing my sense of balance, so I walk with a cane. I can walk about a block, maybe two small ones, but that¢s about it. Stairs are a killer. In September I was hospitalized for 5 days due to the encephalopathy. Currently, I am undergoing my third treatment. This time around I am doing Infergen, which is a daily injectable form of interferon. My second treatment was cut short by the insurance company. I was supposed to go 72 weeks, but they stopped it at 52. After several weeks of fighting with them, I was approved for the full 72 weeks. So, I¢ve been on treatment almost 2 years, with only a short break in-between the two treatments. As my hemoglobin tends to drop, I am also on Procrit. I have great doctors, including a hepatologist and internist. I¢ve had trouble with psychiatrists (I have mental health issues as well) but recently the insurance company approved for me to go see the shrink I¢d seen for many years, but had to stop because of insurance (he¢s not in-network). I¢ve applied for SS disability, but was turned down twice. They said that since I had my arms and legs, I couldn¢t be considered disabled! My attorney is appealing this decision, but my understanding is that we are now waiting for a hearing with a judicial judge which could take up to 2 years. Our money will not last much longer, so this is a source of stress as well. Well, I guess that¢s enough for now. Even typing this much wears me out, though I can work a mouse without too much trouble. J Matchinsky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 And if you get on Disability they cover the dentist, glasses every three years & prescriptions, all I pay is $2/script. They also cover my insulin needles (I'm diabetic) & any other medical stuff like orthotics, incontinence supplies etcSuZie I remember you to Micheal, and am praying things get better for you financially. It is easier in Canada to get our pensions without loosing our arms or legs. It is not easy if you have only hep c unless it causing very bad health issues then you are put on disability but only about $775 per month. If our health issues are bad at least we can go on welfare until our disability kicks in and we get a lump sum back from disability cause they pay back to when you applied and welfare gets their money back off the top. It isn¢t much but it is better then nothing. At least in Canada we only have to pay for our drugs and glasses and dentists if you don¢t have insurance,but all other expenses are paid and there is help here with the extra expenses if needed drug wise. Hoping things are better in the new year and you are in my prayers. Gail -----Original Message----- From: HepatitisCSupportGr oupForDummies@ yahoogroups. com [mailto:HepatitisCS upportGroupForDu mmies@yahoogroup s.com]On Behalf Of Matchinsky Sent: December 11, 2008 7:13 AM To: HepatitisCSupportGr oupForDummies@ yahoogroups. com Subject: [HepatitisCSupportG roupForDummies] Introduction Hi, my name is . I was a member of this group before, but had subscribed to too many groups, and cut this one. I left one of the groups I kept because of a disagreement; a mod was providing false information and insisting it was accurate. My position was and always will be that one should trust their doctor, but if you find you can¢t, then it¢s time to get a new doctor. They¢re only human and they make mistakes but they have the real-world experience (and full background information) to make decisions. Of course, it¢s important to provide that background information. Medicine should make sense, and if it doesn¢t, ask questions or get a second opinion! I am 53 years and married to a wonderfully supportive woman who only happens to be a pediatric nurse. She does look out for me though. She attends all of my appointments, since my memory is at issue. I am also a recovering addict and did anything and everything for 20 years. When I finally went to treatment, I was injecting cocaine, which I am sure is how I contracted this virus. I¢ve been clean and sober for 20 years now. For over 10 years I worked as a substance abuse counselor and went to school, culminating in a Master¢s degree in Addiction Psychology. I¢ve also taught psychology at the local community college. My disease has progressed to Late Stage Liver Disease (LSLD = cirrhosis, but my liver isn¢t in immediate danger of shutting down) and I have developed hepatic encephalopathy, which is doing permanent neurological damage. I can¢t work anymore. My memory is shot, the fog is terrible and I¢m losing my sense of balance, so I walk with a cane. I can walk about a block, maybe two small ones, but that¢s about it. Stairs are a killer. In September I was hospitalized for 5 days due to the encephalopathy. Currently, I am undergoing my third treatment. This time around I am doing Infergen, which is a daily injectable form of interferon. My second treatment was cut short by the insurance company. I was supposed to go 72 weeks, but they stopped it at 52. After several weeks of fighting with them, I was approved for the full 72 weeks. So, I¢ve been on treatment almost 2 years, with only a short break in-between the two treatments. As my hemoglobin tends to drop, I am also on Procrit. I have great doctors, including a hepatologist and internist. I¢ve had trouble with psychiatrists (I have mental health issues as well) but recently the insurance company approved for me to go see the shrink I¢d seen for many years, but had to stop because of insurance (he¢s not in-network). I¢ve applied for SS disability, but was turned down twice. They said that since I had my arms and legs, I couldn¢t be considered disabled! My attorney is appealing this decision, but my understanding is that we are now waiting for a hearing with a judicial judge which could take up to 2 years. Our money will not last much longer, so this is a source of stress as well. Well, I guess that¢s enough for now. Even typing this much wears me out, though I can work a mouse without too much trouble. J Matchinsky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 WELCOME DON 'Be kinder than necessary because everyone you meet is fighting some kind of battle. Subject: INTRODUCTIONTo: HepatitisCSupportGroupForDummies Date: Friday, December 12, 2008, 1:08 PM hi everyone Im don in kansas, friend to debbie[pita54] and michael[m]. Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all. I must say it seems everyone here is alot friendlier. I am 1b-86009 load, with no tx as of yet. Im the guy who wants to send all of you healing energy, love, and no info at all. lol I know little except Im tired and got lotsa fog. I live in salina, ks, by myself. My GF left, and family is far away. I have PTSD, panic attacks, depression, mood swings, all which I take headmeds for. The mental health folks here have been real kind to me, getting me set up with a place to live, and meds, not to mention other services too. I used a needle in the late 60's-early 70's. Last summer was told I had hep c. Ive been clean since early 70's except for pot and cigs. I am just an old hippy. Wont give up my hair and beard. 57 this yr. I havent started tx yet, am concidering it and alternatives, but am seeing docs for info. Im scared, but getting calmer about tx. I just worry alot because Im a 1B, and from what I hear, thats hard to get rid of. Ive been eating everything not nailed down, minus salt, sugar, cafeen, alcohol, drugs, etc. I am glad this site is here, and will try to be worthy of it, but if you push my buttons, I tend to say what I think. [the other site mods didnt like that]. Thank you for allowing me to come here to learn, give and take support, and blast everyone with healing energy. I do believe in God, but thats btwn me and him. I wont cram my beliefs down your throat, but from time to time I may make mention of God. Take it or leave it. Your beliefs are yours with my blessings. I am opinionated too. I do mention my opinions, but never mean disrespect to anyone. Just my thoughts. No more, no less. I realize we are all sick here in one degree or another, and will try to keep the stress at a low ebb. I dont like it either. Anyway, I forgot most of what I had to say, so my blabber is done. love don in kansas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 thank you Are you a moderator, or just super friendly? love don in kansas From: Christ <ludichrist2000@ yahoo.com>Subject: [HepatitisCSupportG roupForDummies] INTRODUCTIONTo: HepatitisCSupportGr oupForDummies@ yahoogroups. comDate: Friday, December 12, 2008, 1:08 PM hi everyone Im don in kansas, friend to debbie[pita54] and michael[m]. Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all. I must say it seems everyone here is alot friendlier. I am 1b-86009 load, with no tx as of yet. Im the guy who wants to send all of you healing energy, love, and no info at all. lol I know little except Im tired and got lotsa fog. I live in salina, ks, by myself. My GF left, and family is far away. I have PTSD, panic attacks, depression, mood swings, all which I take headmeds for. The mental health folks here have been real kind to me, getting me set up with a place to live, and meds, not to mention other services too. I used a needle in the late 60's-early 70's. Last summer was told I had hep c. Ive been clean since early 70's except for pot and cigs. I am just an old hippy. Wont give up my hair and beard. 57 this yr. I havent started tx yet, am concidering it and alternatives, but am seeing docs for info. Im scared, but getting calmer about tx. I just worry alot because Im a 1B, and from what I hear, thats hard to get rid of. Ive been eating everything not nailed down, minus salt, sugar, cafeen, alcohol, drugs, etc. I am glad this site is here, and will try to be worthy of it, but if you push my buttons, I tend to say what I think. [the other site mods didnt like that]. Thank you for allowing me to come here to learn, give and take support, and blast everyone with healing energy. I do believe in God, but thats btwn me and him. I wont cram my beliefs down your throat, but from time to time I may make mention of God. Take it or leave it. Your beliefs are yours with my blessings. I am opinionated too. I do mention my opinions, but never mean disrespect to anyone. Just my thoughts. No more, no less. I realize we are all sick here in one degree or another, and will try to keep the stress at a low ebb. I dont like it either. Anyway, I forgot most of what I had to say, so my blabber is done. love don in kansas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 > > From: Christ <ludichrist2000@ yahoo.com> > Subject: [HepatitisCSupportG roupForDummies] INTRODUCTION > To: HepatitisCSupportGr oupForDummies@ yahoogroups. com > Date: Friday, December 12, 2008, 1:08 PM > > > > > > > > > > hi everyone > Im don in kansas, friend to debbie[pita54] and michael[m]. > Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all. > I must say it seems everyone here is alot friendlier. > I am 1b-86009 load, with no tx as of yet. > Im the guy who wants to send all of you healing energy, love, and no info at all. lol > I know little except Im tired and got lotsa fog. > I live in salina, ks, by myself. My GF left, and family is far away. > I have PTSD, panic attacks, depression, mood swings, all which I take headmeds for. > The mental health folks here have been real kind to me, getting me set up with a place to live, and meds, not to mention other services too. > I used a needle in the late 60's-early 70's. Last summer was told I had hep c. > Ive been clean since early 70's except for pot and cigs. > I am just an old hippy. Wont give up my hair and beard. 57 this yr. > I havent started tx yet, am concidering it and alternatives, but am seeing docs for info. > Im scared, but getting calmer about tx. I just worry alot because Im a 1B, and from what I hear, thats hard to get rid of. > Ive been eating everything not nailed down, minus salt, sugar, cafeen, alcohol, drugs, etc. > I am glad this site is here, and will try to be worthy of it, but if you push my buttons, I tend to say what I think. [the other site mods didnt like that]. > Thank you for allowing me to come here to learn, give and take support, and blast everyone with healing energy. > I do believe in God, but thats btwn me and him. I wont cram my beliefs down your throat, but from time to time I may make mention of God. Take it or leave it. Your beliefs are yours with my blessings. > I am opinionated too. I do mention my opinions, but never mean disrespect to anyone. Just my thoughts. No more, no less. > I realize we are all sick here in one degree or another, and will try to keep the stress at a low ebb. I dont like it either. > Anyway, I forgot most of what I had to say, so my blabber is done. > love > don in kansas > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 I remember you to Micheal, and am praying things get better for you financially. It is easier in Canada to get our pensions without loosing our arms or legs. It is not easy if you have only hep c unless it causing very bad health issues then you are put on disability but only about $775 per month. If our health issues are bad at least we can go on welfare until our disability kicks in and we get a lump sum back from disability cause they pay back to when you applied and welfare gets their money back off the top. It isn’t much but it is better then nothing. At least in Canada we only have to pay for our drugs and glasses and dentists if you don’t have insurance,but all other expenses are paid and there is help here with the extra expenses if needed drug wise. Hoping things are better in the new year and you are in my prayers. Gail -----Original Message----- From: HepatitisCSupportGroupForDummies [mailto:HepatitisCSupportGroupForDummies ]On Behalf Of Matchinsky Sent: December 11, 2008 7:13 AM To: HepatitisCSupportGroupForDummies Subject: Introduction Hi, my name is . I was a member of this group before, but had subscribed to too many groups, and cut this one. I left one of the groups I kept because of a disagreement; a mod was providing false information and insisting it was accurate. My position was and always will be that one should trust their doctor, but if you find you can’t, then it’s time to get a new doctor. They’re only human and they make mistakes but they have the real-world experience (and full background information) to make decisions. Of course, it’s important to provide that background information. Medicine should make sense, and if it doesn’t, ask questions or get a second opinion! I am 53 years and married to a wonderfully supportive woman who only happens to be a pediatric nurse. She does look out for me though. She attends all of my appointments, since my memory is at issue. I am also a recovering addict and did anything and everything for 20 years. When I finally went to treatment, I was injecting cocaine, which I am sure is how I contracted this virus. I’ve been clean and sober for 20 years now. For over 10 years I worked as a substance abuse counselor and went to school, culminating in a Master’s degree in Addiction Psychology. I’ve also taught psychology at the local community college. My disease has progressed to Late Stage Liver Disease (LSLD = cirrhosis, but my liver isn’t in immediate danger of shutting down) and I have developed hepatic encephalopathy, which is doing permanent neurological damage. I can’t work anymore. My memory is shot, the fog is terrible and I’m losing my sense of balance, so I walk with a cane. I can walk about a block, maybe two small ones, but that’s about it. Stairs are a killer. In September I was hospitalized for 5 days due to the encephalopathy. Currently, I am undergoing my third treatment. This time around I am doing Infergen, which is a daily injectable form of interferon. My second treatment was cut short by the insurance company. I was supposed to go 72 weeks, but they stopped it at 52. After several weeks of fighting with them, I was approved for the full 72 weeks. So, I’ve been on treatment almost 2 years, with only a short break in-between the two treatments. As my hemoglobin tends to drop, I am also on Procrit. I have great doctors, including a hepatologist and internist. I’ve had trouble with psychiatrists (I have mental health issues as well) but recently the insurance company approved for me to go see the shrink I’d seen for many years, but had to stop because of insurance (he’s not in-network). I’ve applied for SS disability, but was turned down twice. They said that since I had my arms and legs, I couldn’t be considered disabled! My attorney is appealing this decision, but my understanding is that we are now waiting for a hearing with a judicial judge which could take up to 2 years. Our money will not last much longer, so this is a source of stress as well. Well, I guess that’s enough for now. Even typing this much wears me out, though I can work a mouse without too much trouble. J Matchinsky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 hi Tomas I just tried to e-mail you at the address you gave and got the failure demon. It doesnt seem to be the correct e-mail. Ive been trying to find someone close to talk to about stuff. There is no support grp in the salina area anymore. Can you contact me please? I need to know stuff about this area. love don in kansas. Subject: Re: INTRODUCTIONTo: HepatitisCSupportGroupForDummies Date: Friday, December 12, 2008, 5:50 PM > > From: Christ <ludichrist2000@ yahoo.com>> Subject: [HepatitisCSupportG roupForDummies] INTRODUCTION> To: HepatitisCSupportGr oupForDummies@ yahoogroups. com> Date: Friday, December 12, 2008, 1:08 PM> > > > > > > > > > hi everyone> Im don in kansas, friend to debbie[pita54] and michael[m].> Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all.> I must say it seems everyone here is alot friendlier.> I am 1b-86009 load, with no tx as of yet.> Im the guy who wants to send all of you healing energy, love, and no info at all. lol> I know little except Im tired and got lotsa fog.> I live in salina, ks, by myself. My GF left, and family is far away.> I have PTSD, panic attacks, depression, mood swings, all which I take headmeds for.> The mental health folks here have been real kind to me, getting me set up with a place to live, and meds, not to mention other services too.> I used a needle in the late 60's-early 70's. Last summer was told I had hep c.> Ive been clean since early 70's except for pot and cigs.> I am just an old hippy. Wont give up my hair and beard. 57 this yr.> I havent started tx yet, am concidering it and alternatives, but am seeing docs for info.> Im scared, but getting calmer about tx. I just worry alot because Im a 1B, and from what I hear, thats hard to get rid of.> Ive been eating everything not nailed down, minus salt, sugar, cafeen, alcohol, drugs, etc.> I am glad this site is here, and will try to be worthy of it, but if you push my buttons, I tend to say what I think. [the other site mods didnt like that].> Thank you for allowing me to come here to learn, give and take support, and blast everyone with healing energy.> I do believe in God, but thats btwn me and him. I wont cram my beliefs down your throat, but from time to time I may make mention of God. Take it or leave it. Your beliefs are yours with my blessings.> I am opinionated too. I do mention my opinions, but never mean disrespect to anyone. Just my thoughts. No more, no less.> I realize we are all sick here in one degree or another, and will try to keep the stress at a low ebb. I dont like it either.> Anyway, I forgot most of what I had to say, so my blabber is done.> love> don in kansas> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 13, 2008 Report Share Posted December 13, 2008 Hey Don! You might not wanna tell people that you & I are friends. You saw where that got us at the other group!...LOL...just teasing...Debbie- -- In HepatitisCSupportGroupForDummies , Christ wrote: > > hi everyone > Im don in kansas, friend to debbie[pita54] and michael[m]. > Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all. > I must say it seems everyone here is alot friendlier. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 13, 2008 Report Share Posted December 13, 2008 hi Gail Thank you for the warm welcome. I know you now too. lol Im glad to hear you were able to beat the beast. It gives me hope for when my time comes. Half of the ppl I talk to say 1B geno is hard to clear. This causes me worry. I dont want to go thru a year just to lose in the end. I am already on zoloft antidepressant, seroquil for mood stablization/sleep, and ativan for PTSD/panic. Im pretty stable as long as I dont think. At least Im not trying to kill myself, or crying all the time. Once in awhile I can get out of my house, grocerys, trash, mail. I have another doc appmt next month when my pnumonia should be cleared up, and my records transfered to this new doc here. They may want me to do labs then too. I dont know. The doc here said he has 10-12 hep c patients, so hopefully he knows his stuff. I am watching my diet, no salt, less sugar, more liquids, less red meat, lots more fruit, and grains. I am eating ok. I hardly get out of bed so Im getting plenty of rest. Got alot of tiredness and brain fog. I met Tomas here too, and he lives just down the road from me 35 miles or so. He is a non-responder, but has done tx, so he should be able to help me with questions about tx. Not to mention others here. I want to thank you all for your support and info. In return I support you all, and send each and everyone of you healing energy. May God be kind to you all. I love you all, you are my family and my friends. I am pretty much alone facing this. My GF broke up with me [she cant deal], and my blood family live far away. Have no friends so far to just hang with. Do have folks at the mental health place I go to, staff and nuts. lol Dont want to just hang with either. Staff want me to be someone Im not, and the nuts have their own troubles. Im just waiting to see where this road leads. Hopefully to a good place. ok Ive blabbed. love don in kansas Subject: RE: INTRODUCTIONTo: HepatitisCSupportGroupForDummies Date: Saturday, December 13, 2008, 3:04 PM Welcome to our group.You know some of the people here from what I understand, so you know we are a family here and a little on the crazy side half the time. We are fortunate enough to really have a great group of people here and you can win this battle. I am genotype 1 and was treated with interferon and riboveron for 52wks in 98-99 and have been undetectable since. There is a 50% success rate with treatment for genotype 1 and even if the treatment doesn¢t work, your liver is healing. Treatment can really be hard on the head because the chemicals seem to cause depression and anger etc. Normally anti depressants are used to control that aspect of treatment,so you will have to have your doctor that is helping with your emotional problems work with the hep doctor to make sure the balance is kept in check. We have people here that are by polar etc and it is hard to get that even balance. Keep the faith my friend cause that sure helps through treatment and start with drinking lots of water now. I gallon of water through out the day is what is required to help wash the sides of treatment aside so that they are not as bad. Take care and we are here if you need us. If you are having memory problems yet,get someone to go with you to the hep specialist to refresh your memory. Gail [HepatitisCSupportG roupForDummies] INTRODUCTION hi everyone Im don in kansas, friend to debbie[pita54] and michael[m]. Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all. I must say it seems everyone here is alot friendlier. I am 1b-86009 load, with no tx as of yet. Im the guy who wants to send all of you healing energy, love, and no info at all. lol I know little except Im tired and got lotsa fog. I live in salina, ks, by myself. My GF left, and family is far away. I have PTSD, panic attacks, depression, mood swings, all which I take headmeds for. The mental health folks here have been real kind to me, getting me set up with a place to live, and meds, not to mention other services too. I used a needle in the late 60's-early 70's. Last summer was told I had hep c. Ive been clean since early 70's except for pot and cigs. I am just an old hippy. Wont give up my hair and beard. 57 this yr. I havent started tx yet, am concidering it and alternatives, but am seeing docs for info. Im scared, but getting calmer about tx. I just worry alot because Im a 1B, and from what I hear, thats hard to get rid of. Ive been eating everything not nailed down, minus salt, sugar, cafeen, alcohol, drugs, etc. I am glad this site is here, and will try to be worthy of it, but if you push my buttons, I tend to say what I think. [the other site mods didnt like that]. Thank you for allowing me to come here to learn, give and take support, and blast everyone with healing energy. I do believe in God, but thats btwn me and him. I wont cram my beliefs down your throat, but from time to time I may make mention of God. Take it or leave it. Your beliefs are yours with my blessings. I am opinionated too. I do mention my opinions, but never mean disrespect to anyone. Just my thoughts. No more, no less. I realize we are all sick here in one degree or another, and will try to keep the stress at a low ebb. I dont like it either. Anyway, I forgot most of what I had to say, so my blabber is done. love don in kansas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 13, 2008 Report Share Posted December 13, 2008 hi Vickie Glad to meet you. Thank you for welcoming me to the group. Im also glad because your the first 1B [like me] I think that Ive talked to that has tx and cleared. Congrats and more. This gives me hope that I too can clear once I do tx. I too am a quiet person, deep thinker, and Im into God, but not religion. Just an old hippy 57, who is trying to figure it all out....still. I lurk mostly too, unless someone says something to me, or I see a chance to give out some good energy, or an opinion. lol And 59 isnt old....its just right. We must become friends. I insist. We may never meet but we can talk. If you need me for anything, just hollar. I will answer. Plus you have my e-mail. love don in kansas Subject: Re: INTRODUCTIONTo: HepatitisCSupportGroupForDummies Date: Saturday, December 13, 2008, 9:04 AM Hi, Don. I'm VickieG, 59 (ouch!) geno type 1b. I finished 48 week tx the end of last May undetectable. I went last Thursday for my six month followup and will get results either Monday or Tuesday next week. There is always hope that we will stay undetectable. I'm a very quiet person, deep thinker and also believe in God. I lurk more than I participate since I finished tx, as I don't really have much to contribute now. I welcome you to our group. Hugs, VickieG From: Christ <ludichrist2000@ yahoo.com>To: HepatitisCSupportGr oupForDummies@ yahoogroups. comSent: Friday, December 12, 2008 3:08:15 PMSubject: [HepatitisCSupportG roupForDummies] INTRODUCTION hi everyone Im don in kansas, friend to debbie[pita54] and michael[m]. Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all. I must say it seems everyone here is alot friendlier. I am 1b-86009 load, with no tx as of yet. Im the guy who wants to send all of you healing energy, love, and no info at all. lol I know little except Im tired and got lotsa fog. I live in salina, ks, by myself. My GF left, and family is far away. I have PTSD, panic attacks, depression, mood swings, all which I take headmeds for. The mental health folks here have been real kind to me, getting me set up with a place to live, and meds, not to mention other services too. I used a needle in the late 60's-early 70's. Last summer was told I had hep c. Ive been clean since early 70's except for pot and cigs. I am just an old hippy. Wont give up my hair and beard. 57 this yr. I havent started tx yet, am concidering it and alternatives, but am seeing docs for info. Im scared, but getting calmer about tx. I just worry alot because Im a 1B, and from what I hear, thats hard to get rid of. Ive been eating everything not nailed down, minus salt, sugar, cafeen, alcohol, drugs, etc. I am glad this site is here, and will try to be worthy of it, but if you push my buttons, I tend to say what I think. [the other site mods didnt like that]. Thank you for allowing me to come here to learn, give and take support, and blast everyone with healing energy. I do believe in God, but thats btwn me and him. I wont cram my beliefs down your throat, but from time to time I may make mention of God. Take it or leave it. Your beliefs are yours with my blessings. I am opinionated too. I do mention my opinions, but never mean disrespect to anyone. Just my thoughts. No more, no less. I realize we are all sick here in one degree or another, and will try to keep the stress at a low ebb. I dont like it either. Anyway, I forgot most of what I had to say, so my blabber is done. love don in kansas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 13, 2008 Report Share Posted December 13, 2008 Welcome to our group.You know some of the people here from what I understand, so you know we are a family here and a little on the crazy side half the time. We are fortunate enough to really have a great group of people here and you can win this battle. I am genotype 1 and was treated with interferon and riboveron for 52wks in 98-99 and have been undetectable since. There is a 50% success rate with treatment for genotype 1 and even if the treatment doesn’t work, your liver is healing. Treatment can really be hard on the head because the chemicals seem to cause depression and anger etc. Normally anti depressants are used to control that aspect of treatment,so you will have to have your doctor that is helping with your emotional problems work with the hep doctor to make sure the balance is kept in check. We have people here that are by polar etc and it is hard to get that even balance. Keep the faith my friend cause that sure helps through treatment and start with drinking lots of water now. I gallon of water through out the day is what is required to help wash the sides of treatment aside so that they are not as bad. Take care and we are here if you need us. If you are having memory problems yet,get someone to go with you to the hep specialist to refresh your memory. Gail -----Original Message----- From: HepatitisCSupportGroupForDummies [mailto:HepatitisCSupportGroupForDummies ]On Behalf Of Christ Sent: December 12, 2008 1:08 PM To: HepatitisCSupportGroupForDummies Subject: INTRODUCTION hi everyone Im don in kansas, friend to debbie[pita54] and michael[m]. Too much hassle at the other site[HcC] so I came here. Altho I still lurk there and give support to all. I must say it seems everyone here is alot friendlier. I am 1b-86009 load, with no tx as of yet. Im the guy who wants to send all of you healing energy, love, and no info at all. lol I know little except Im tired and got lotsa fog. I live in salina, ks, by myself. My GF left, and family is far away. I have PTSD, panic attacks, depression, mood swings, all which I take headmeds for. The mental health folks here have been real kind to me, getting me set up with a place to live, and meds, not to mention other services too. I used a needle in the late 60's-early 70's. Last summer was told I had hep c. Ive been clean since early 70's except for pot and cigs. I am just an old hippy. Wont give up my hair and beard. 57 this yr. I havent started tx yet, am concidering it and alternatives, but am seeing docs for info. Im scared, but getting calmer about tx. I just worry alot because Im a 1B, and from what I hear, thats hard to get rid of. Ive been eating everything not nailed down, minus salt, sugar, cafeen, alcohol, drugs, etc. I am glad this site is here, and will try to be worthy of it, but if you push my buttons, I tend to say what I think. [the other site mods didnt like that]. Thank you for allowing me to come here to learn, give and take support, and blast everyone with healing energy. I do believe in God, but thats btwn me and him. I wont cram my beliefs down your throat, but from time to time I may make mention of God. Take it or leave it. Your beliefs are yours with my blessings. I am opinionated too. I do mention my opinions, but never mean disrespect to anyone. Just my thoughts. No more, no less. I realize we are all sick here in one degree or another, and will try to keep the stress at a low ebb. I dont like it either. Anyway, I forgot most of what I had to say, so my blabber is done. love don in kansas Quote Link to comment Share on other sites More sharing options...
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