Guest guest Posted December 21, 2000 Report Share Posted December 21, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page From: GSTahoe@... > I just thought maybe someone knows > of somewhere you can get assistance. would appreciate any help. Oh yea she > is in ohio in case maybe there is some type of help in that state. > Have your friend check with her Gastroenterologist about FDA research for the approval of new Interferon drugs. The drug companies have programs where you can volunteer to try new forms of interferon, i.e., pegylated interferon, and they will pay for part or all of the bill. ********************************* Contact Schering for Friend's Meds From: jc2000inpa@... Hi...have your friend call the Commitment to Care Program @ Schering-Plough. It is a program to help those who cannot afford their meds. Also go to Hepatitis Neighborhood, go to the Priority Med Section and they too, have a program to help with acquiring meds, for low-income people. I do believe that both will even handle the contacting the insurance company and working out the details. The ordering physician may also have to get involved, by writing a medically necessary letter to the insurance company. If you do not have the addresses, let me know and I can send them to you...just to early to turn on all those bright lights...didn't sleep well, and hoping to answer a few mails and get a few more hours of shuteye. Let me know, if I can help. Remember we are never alone when we are here ....JUNE ********************************* From: nightsky@... Hello, Schering Plough has programs to help people who cannot afford or do not have insurance coverage. This was a couple of years ago but I don't think that is a problem. Call: 1-800 222-7579 or 1-800-483-6760. Someone will lead you in the right direction. Good Luck, ********************************* From: jdaly@... Priority Health care works with my insurance directly to receive payment. At first my insurance said they would not pay the costs at all. At this time 11 months into treatment they have been paying. You can reach Priority Healthcare Corp @ 877-761-4743, they are located in Lake , FL 32746. Good Luck to your friend, she is lucky to have you. ********************************* From: objectivemedicine@... In answer to the question about financial assistance, there is a helpful link in the Hepatitis Database go to: http://www.objectivemedicine.com/dbsearch.htm Then select: Support Groups Financial Help R ********************************* From: Cozzzyyy@... I am on treatment but my insurance covers 100% which I am very fortunate......Let your friend know if she needs someone to talk with she can with me. The first night will be her worst....but the next day it gets better. Cosy ********************************* Drug Discovery Programs <A HREF= " http://www.ptcbio.com/antiv.html " >http://www.ptcbio.com/antiv.html </A> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2000 Report Share Posted December 21, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page From: GSTahoe@... > I just thought maybe someone knows > of somewhere you can get assistance. would appreciate any help. Oh yea she > is in ohio in case maybe there is some type of help in that state. > Have your friend check with her Gastroenterologist about FDA research for the approval of new Interferon drugs. The drug companies have programs where you can volunteer to try new forms of interferon, i.e., pegylated interferon, and they will pay for part or all of the bill. ********************************* Contact Schering for Friend's Meds From: jc2000inpa@... Hi...have your friend call the Commitment to Care Program @ Schering-Plough. It is a program to help those who cannot afford their meds. Also go to Hepatitis Neighborhood, go to the Priority Med Section and they too, have a program to help with acquiring meds, for low-income people. I do believe that both will even handle the contacting the insurance company and working out the details. The ordering physician may also have to get involved, by writing a medically necessary letter to the insurance company. If you do not have the addresses, let me know and I can send them to you...just to early to turn on all those bright lights...didn't sleep well, and hoping to answer a few mails and get a few more hours of shuteye. Let me know, if I can help. Remember we are never alone when we are here ....JUNE ********************************* From: nightsky@... Hello, Schering Plough has programs to help people who cannot afford or do not have insurance coverage. This was a couple of years ago but I don't think that is a problem. Call: 1-800 222-7579 or 1-800-483-6760. Someone will lead you in the right direction. Good Luck, ********************************* From: jdaly@... Priority Health care works with my insurance directly to receive payment. At first my insurance said they would not pay the costs at all. At this time 11 months into treatment they have been paying. You can reach Priority Healthcare Corp @ 877-761-4743, they are located in Lake , FL 32746. Good Luck to your friend, she is lucky to have you. ********************************* From: objectivemedicine@... In answer to the question about financial assistance, there is a helpful link in the Hepatitis Database go to: http://www.objectivemedicine.com/dbsearch.htm Then select: Support Groups Financial Help R ********************************* From: Cozzzyyy@... I am on treatment but my insurance covers 100% which I am very fortunate......Let your friend know if she needs someone to talk with she can with me. The first night will be her worst....but the next day it gets better. Cosy ********************************* Drug Discovery Programs <A HREF= " http://www.ptcbio.com/antiv.html " >http://www.ptcbio.com/antiv.html </A> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2000 Report Share Posted December 22, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page From: energymc@... Why on earth was this posted? What the hell does this person's opinion have to do with reality? By the way, I thought the election was over. Silly me. Carol ----- Original Message ----- > clinton's health care plan > > From: Neil315@... > DO NOT BELIEVE ME > educate yourself.bill and hillary's health care plan had a cap on services > and an age limit on transplant's- too old --tough.it was rationed health care > for us but not for her and bill and the rest of the washington crowd--they > were exempt. DO NOT BELIEVE HIM. Educate yourself. The above statement is not his opinion, it’s a fact. You should be able to find Hillary’s health care proposal on the internet somewhere. Merry Christmas, Chuck Demastus Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2000 Report Share Posted December 22, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page From: energymc@... Why on earth was this posted? What the hell does this person's opinion have to do with reality? By the way, I thought the election was over. Silly me. Carol ----- Original Message ----- > clinton's health care plan > > From: Neil315@... > DO NOT BELIEVE ME > educate yourself.bill and hillary's health care plan had a cap on services > and an age limit on transplant's- too old --tough.it was rationed health care > for us but not for her and bill and the rest of the washington crowd--they > were exempt. DO NOT BELIEVE HIM. Educate yourself. The above statement is not his opinion, it’s a fact. You should be able to find Hillary’s health care proposal on the internet somewhere. Merry Christmas, Chuck Demastus Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2000 Report Share Posted December 23, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page Hillary’s Health Care Plan ***************************************** From: Angls4Hope@... Thanks for this post Chuck and a reminder of educating and empowering yourselves. Unfortunately, we are getting slammed from all sides by our governement with our healthcare and personally I DO NOT TRUST any of them. Angel Huggzz ~~~~~~~~~~~~~~~~~~~~~~~~ From: lewtom@... Is this site a political forum or a health forum? Let's stick to HCV info!!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2000 Report Share Posted December 23, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page Hillary’s Health Care Plan ***************************************** From: Angls4Hope@... Thanks for this post Chuck and a reminder of educating and empowering yourselves. Unfortunately, we are getting slammed from all sides by our governement with our healthcare and personally I DO NOT TRUST any of them. Angel Huggzz ~~~~~~~~~~~~~~~~~~~~~~~~ From: lewtom@... Is this site a political forum or a health forum? Let's stick to HCV info!!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2000 Report Share Posted December 29, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page Re: Newly-Identified Virus May Cause Hepatitis From: nightsky@... Hi , I am sure not happy to see this. Remember the blood transfusion I had due to the GI Bleed in Oct. Does this mean I could have gotten another Hepatitis?? This SEN-V doesn't have a screening test yet does it. Not panic, just anxious. ************************************** Re: Stealth Invaders From: Neil315@... great new's---after 3 month's of combo therapy my viral count is undetectable.the dr.will still keep me on med's for the rest of the 48 week treatment due to the amount of damage to my liver. neil Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2000 Report Share Posted December 29, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page Re: Newly-Identified Virus May Cause Hepatitis From: nightsky@... Hi , I am sure not happy to see this. Remember the blood transfusion I had due to the GI Bleed in Oct. Does this mean I could have gotten another Hepatitis?? This SEN-V doesn't have a screening test yet does it. Not panic, just anxious. ************************************** Re: Stealth Invaders From: Neil315@... great new's---after 3 month's of combo therapy my viral count is undetectable.the dr.will still keep me on med's for the rest of the 48 week treatment due to the amount of damage to my liver. neil Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2000 Report Share Posted December 29, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page From: WKeller2@... I have had Hep C for at least 16 years. They believe it could be even longer. We are not sure how I contacted it, but out of three children, my 15 year old also has it. He had a liver biopsy last January and luckily it showed no signs of liver damage (inflammation was present) This was done because of fluxuating liver enzyme levels. Because this was so rare in a child the doctor that was following my son and I together. He wanted to start my son on treatment this past June, but would not agree to a biopsy. I had to take him to two other doctors before I found one that would agree to the biopsy. I wanted another opinion and the biopsy before I made the decision on the treatment. I just didn't want to put him through it if we could avoid it for now. It is a decision I will always be glad I made. At least for now. My levels (done every 6 months)have always read high in the normal range. But for the past few months I have been tired, my bones aching and my memory has gotten really bad off and on. I have just turned 40 and just believe it's something besides getting older. I just read where Hep C can cause these symptoms. My doctor (just like my son)does not feel cause for a biopsy. Do you think I should try to find one that will agree to give me one? I try to keep up with all the information your group sends, but dealing with referrals, etc. makes it hard to decide whether I should pursue a second opinion. I have read that just because the levels are normal, it doesn't mean that there isn't damage occurring. Could it be that the sluggishness, forgetfulness and aching bones are really a part of this disease for me even though my levels are normal? I appreciate any thoughts you have. Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2000 Report Share Posted December 29, 2000 [hepati] Comments from ya'll My Groups | HepC Main Page From: WKeller2@... I have had Hep C for at least 16 years. They believe it could be even longer. We are not sure how I contacted it, but out of three children, my 15 year old also has it. He had a liver biopsy last January and luckily it showed no signs of liver damage (inflammation was present) This was done because of fluxuating liver enzyme levels. Because this was so rare in a child the doctor that was following my son and I together. He wanted to start my son on treatment this past June, but would not agree to a biopsy. I had to take him to two other doctors before I found one that would agree to the biopsy. I wanted another opinion and the biopsy before I made the decision on the treatment. I just didn't want to put him through it if we could avoid it for now. It is a decision I will always be glad I made. At least for now. My levels (done every 6 months)have always read high in the normal range. But for the past few months I have been tired, my bones aching and my memory has gotten really bad off and on. I have just turned 40 and just believe it's something besides getting older. I just read where Hep C can cause these symptoms. My doctor (just like my son)does not feel cause for a biopsy. Do you think I should try to find one that will agree to give me one? I try to keep up with all the information your group sends, but dealing with referrals, etc. makes it hard to decide whether I should pursue a second opinion. I have read that just because the levels are normal, it doesn't mean that there isn't damage occurring. Could it be that the sluggishness, forgetfulness and aching bones are really a part of this disease for me even though my levels are normal? I appreciate any thoughts you have. Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2001 Report Share Posted January 1, 2001 [hepati] Comments from ya'll My Groups | HepC Main Page Re: Holistic Way From: CANDACEMORAN@... I read the first post. What is Coenzyme Q12? Bob ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Coenzyme Q10 (ubiquinone/ubiquinol) is a fat-soluble quinone with a structure similar to that of vitamin K. It is a powerful antioxidant both on its own and in combination with vitamin E and is vital in powering the body's energy production (ATP) cycle. CoQ10 is found throughout the body in cell membranes, especially in the mitochondrial membranes and is particularly abundant in the heart, lungs, liver, kidneys, spleen, pancreas and adrenal glands. The total body content of CoQ10 is only about 500-1500 mg and decreases with age(5). http://www.yourhealthbase.com/coenzyme_Q10.html **************************************** From: makwa@... Please get another doctor asap. You need to know the condition of your liver to be able to make any treatment decisions. You can have normal lft's and still develop fibrosis and cirrhosis. My first doctor refused to do a biopsy. He said I had a history of depression and wouldn't treat me so why do a biopsy !!! Four years later I get a biopsy and I have cirrhosis. My lft's were never very high, 10-20 points above normal. Please don't make the same mistake I did.... learn all you can and take charge of your medical care. Remember the doctor works for you. hugs, Judy " He who knows others is wise; / He knows himself is enlightened. " --Lao-Tzu ********************************************** From: deboerm@... egroups RE: Holistic article that was just posted. Hmmm, well, I am wondering why they recommend atleast 8 oz. of water a day on that article. Eight oz of water a day would not be enough for anyone, especially those of us with health concerns. It's actually atleast 48 oz a day, if I remember right. Now some days I don't drink quite that much, but pretty close, otherwise I feel bad. I also think that CoQ10 is very important, I see it listed, but not in the important list. I've talked to alot of people that take CoQ10 and have hep c, and it definetly improves our energy level. Sometimes I forget mine, oops! well, that's when I forget to take my Ginko Biloba, my brain pill. Echinecea is a great one, I start taking mine at the first sign of a cold and it nips it in the bud. I also give it to my kids when they need it and all 3 that are in school have had perfect attendence this year so far!! Sometimes I take it just when I'm feeling blah. I guess we can't take it long term, but here and there, so I settle for that. Anyway, I believe it's 6- 8oz glasses of water a day!! Take care, Sherry Quote Link to comment Share on other sites More sharing options...
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