Guest guest Posted June 30, 2009 Report Share Posted June 30, 2009 Too many too soon! My daughter is 4 and is vaccine free and my baby is 2 and a half (can you believe that!!!????) has non either. They are both smarter and healthier than all three of my boys were at these ages. I think vas are important, but we need to push for safer vaccines and schedules. Chuck you may be able to help me with my next question. Dr suggests getting an acellular not a whole cell pertussis vaccine. What does that mean? Gracias! http://www.lewrockwell.com/miller/miller15.html CW -- Re: ? Eight years ago, when my friend had her child, we talked about vaccines, and read about the problems some of the children had and my friend decided to get less vaccines in one shot, and spaced out the ones that her child did get longer than usual. I agreed with her, and thank heaven her child is fine. Roni <>Just because something isn't seen doesn't mean it's not there<> > > > Does anyone know of a good medical website (not web MD or the > likes), but > like a research site. Now that my daughter is 4 I want to start a > vaccine > schedule, but want good research info to compare to what I already > have. > Thanks > CW > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 30, 2009 Report Share Posted June 30, 2009 Crystal, You wrote: > > ....Dr > suggests getting an acellular not a whole cell pertussis vaccine. What does > that mean? Just as it sounds, the whole cell vaccine is made by killing Bordetella pertussis bacteria. The acellular types (more than one) are made from denatured pertussis toxin (something the bacterium produces) mixed with various proteins taken from the cell membrane or fibers. Acellular vaccines were introduced in 1997 to avoid some of the bad reactions to the whole cell vaccines. As I recall, though, the acellular vaccines were also slightly less effective for infants but even more effective for older children. Part of the confusion in results comes from the fact that the FDA licenses combination vaccines with diphtheria and tetanus. You can't pick a combination of this company's diphtheria with that company's acellular pertussis. Anyway, if you are immunizing infants with an acellular, you should plan on multiple booster shots. Chuck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 30, 2009 Report Share Posted June 30, 2009 Oh yeah that is just how it sounds, silly me : ) I think you can get the diptheria and the pertussis separate from the tetanus. Thanks! CW -- Re: ? Crystal, You wrote: > > ....Dr > suggests getting an acellular not a whole cell pertussis vaccine. What does > that mean? Just as it sounds, the whole cell vaccine is made by killing Bordetella pertussis bacteria. The acellular types (more than one) are made from denatured pertussis toxin (something the bacterium produces) mixed with various proteins taken from the cell membrane or fibers. Acellular vaccines were introduced in 1997 to avoid some of the bad reactions to the whole cell vaccines. As I recall, though, the acellular vaccines were also slightly less effective for infants but even more effective for older children. Part of the confusion in results comes from the fact that the FDA licenses combination vaccines with diphtheria and tetanus. You can't pick a combination of this company's diphtheria with that company's acellular pertussis. Anyway, if you are immunizing infants with an acellular, you should plan on multiple booster shots. Chuck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2009 Report Share Posted July 1, 2009 Crystal, You wrote: > > Oh yeah that is just how it sounds, silly me : ) I think you can get the > diptheria and the pertussis separate from the tetanus. Thanks! I believe you can only get the acellular pertussis in combination. If you get pertussis separately, it has to be the whole cell. At any rate that was how it used to be. Maybe they have a new license. At any rate neither DPT nor DPaT (acellular) contain thymerosol. Chuck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2009 Report Share Posted August 17, 2009 sounds like it could be! those are def some of the symptoms....and you know what they say if you havent been told its all in your head you dont have lyme, thats just a joke umong some of us lymies...good luckk Begley - Temporary Placement Manager From: Geri Logan <hotwheels@...> Subject: [ ] ? Date: Monday, August 17, 2009, 4:09 PM Â Group, My friend is very sick today..W/a fever and chills..Is this part of lymes?We have for some time suspected that he has Lymes but has not been able to get help. His doc thinks it is all in his mind, I see Russ being in more pain as time goes on..today he can hardly walk and even his skin hurts part of limes?...... .What to do? Limited Ins! and he hasn't much money. Don't know how to get the doc to hear him!With out him think he is crazy! Thanks Geri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2009 Report Share Posted August 17, 2009 Sounds like its possible. I would suggest going to an LLMD and see what he/she says. It took me years to find out, even went to the best docs in New York, some said it was in my head, and others said I need a vacation, I worked to hard, and throw in CFS and Fibro etc. Only when I went to a LLMD in New Jersey was I diagnosed with Lyme and co-infections. So I suggest getting checked for co-infections also, for that too can create a whole bunch of other problems. Good luck to your friend in this journey.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2009 Report Share Posted August 18, 2009 We need to find a LLMD to call, in our area. Little Falls Minnesota....he is still.sick. Geri Sounds like its possible. I would suggest going to an LLMD and see what he/she says. It took me years to find out, even went to the best docs in New York, some said it was in my head, and others said I need a vacation, I worked to hard, and throw in CFS and Fibro etc. Only when I went to a LLMD in New Jersey was I diagnosed with Lyme and co-infections. So I suggest getting checked for co-infections also, for that too can create a whole bunch of other problems. Good luck to your friend in this journey.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2009 Report Share Posted August 18, 2009 My brother is located in MN and treats lyme: Sult, MD[image: Photo of Sult] *Integracare* 100 2nd St S Sartell, MN 56377 Phone: *(320) 251-2600* To On Mon, Aug 17, 2009 at 11:22 PM, Geri Logan <hotwheels@...> wrote: > > > > We need to find a LLMD to call, in our area. > Little Falls Minnesota....he is still.sick. > Geri > > Sounds like its possible. I would suggest going to an LLMD and see what > he/she says. It took me years to find out, even went to the best docs in New > York, some said it was in my head, and others said I need a vacation, I > worked to hard, and throw in CFS and Fibro etc. Only when I went to a LLMD > in New Jersey was I diagnosed with Lyme and co-infections. So I suggest > getting checked for co-infections also, for that too can create a whole > bunch of other problems. > Good luck to your friend in this journey.... > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2009 Report Share Posted August 18, 2009 Dr Sult is no longer taking lymes patents at this time my mom goes to him and that's what the nurse told said.It is very expensive but then she is lucky to have good ins..I think we may be in trouble that way.Going to call and see. Thank you Geri My brother is located in MN and treats lyme: Sult, MD[image: Photo of Sult] *Integracare* 100 2nd St S Sartell, MN 56377 Phone: *(320) 251-2600* To On Mon, Aug 17, 2009 at 11:22 PM, Geri Logan <hotwheels@...> wrote: > > > > We need to find a LLMD to call, in our area. > Little Falls Minnesota....he is still.sick. > Geri > > Sounds like its possible. I would suggest going to an LLMD and see what > he/she says. It took me years to find out, even went to the best docs in New > York, some said it was in my head, and others said I need a vacation, I > worked to hard, and throw in CFS and Fibro etc. Only when I went to a LLMD > in New Jersey was I diagnosed with Lyme and co-infections. So I suggest > getting checked for co-infections also, for that too can create a whole > bunch of other problems. > Good luck to your friend in this journey.... > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2009 Report Share Posted August 18, 2009 It [robabyl wasn't the best idea to post such information on a public site \like this. Theres no telling who could get a hold on where his practice is and what they do now. Anyway i just urge you do that through private email, because it could be detramental to your brother's practice possibly. Not to be all know-it-all, but you never know. I am not one to think bad, but it is good to be safe. Good luck Geri! \Elaina > > > > We need to find a LLMD to call, in our area. > Little Falls Minnesota... .he is still.sick. > Geri > > Sounds like its possible. I would suggest going to an LLMD and see what > he/she says. It took me years to find out, even went to the best docs in New > York, some said it was in my head, and others said I need a vacation, I > worked to hard, and throw in CFS and Fibro etc. Only when I went to a LLMD > in New Jersey was I diagnosed with Lyme and co-infections. So I suggest > getting checked for co-infections also, for that too can create a whole > bunch of other problems. > Good luck to your friend in this journey.... > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2009 Report Share Posted August 19, 2009 Well, they be able to refer to you someone else who is lyme savy.. Good luck! On Tue, Aug 18, 2009 at 9:35 AM, Geri Logan <hotwheels@...> wrote: > > > > Dr Sult is no longer taking lymes patents at this time my mom goes to him > and that's what the nurse told said.It is very expensive but then she is > lucky to have good ins..I think we may be in trouble that way.Going to call > and see. > Thank you > Geri > > > My brother is located in MN and treats lyme: > Sult, MD[image: Photo of Sult] > *Integracare* > 100 2nd St S > Sartell, MN 56377 > > Phone: *(320) 251-2600* > > To > > On Mon, Aug 17, 2009 at 11:22 PM, Geri Logan <hotwheels@...<hotwheels%40brainerd.net>> > wrote: > > > > > > > > > We need to find a LLMD to call, in our area. > > Little Falls Minnesota....he is still.sick. > > Geri > > > > Sounds like its possible. I would suggest going to an LLMD and see what > > he/she says. It took me years to find out, even went to the best docs in > New > > York, some said it was in my head, and others said I need a vacation, I > > worked to hard, and throw in CFS and Fibro etc. Only when I went to a > LLMD > > in New Jersey was I diagnosed with Lyme and co-infections. So I suggest > > getting checked for co-infections also, for that too can create a whole > > bunch of other problems. > > Good luck to your friend in this journey.... > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2009 Report Share Posted August 19, 2009 we are trying,problen is..INS also! The lymes docs are very far away ....... Geri Well, they be able to refer to you someone else who is lyme savy.. Good luck! On Tue, Aug 18, 2009 at 9:35 AM, Geri Logan <hotwheels@...> wrote: > > > > Dr Sult is no longer taking lymes patents at this time my mom goes to him > and that's what the nurse told said.It is very expensive but then she is > lucky to have good ins..I think we may be in trouble that way.Going to call > and see. > Thank you > Geri > > > My brother is located in MN and treats lyme: > Sult, MD[image: Photo of Sult] > *Integracare* > 100 2nd St S > Sartell, MN 56377 > > Phone: *(320) 251-2600* > > To > > On Mon, Aug 17, 2009 at 11:22 PM, Geri Logan <hotwheels@...<hotwheels%40brainerd.net>> > wrote: > > > > > > > > > We need to find a LLMD to call, in our area. > > Little Falls Minnesota....he is still.sick. > > Geri > > > > Sounds like its possible. I would suggest going to an LLMD and see what > > he/she says. It took me years to find out, even went to the best docs in > New > > York, some said it was in my head, and others said I need a vacation, I > > worked to hard, and throw in CFS and Fibro etc. Only when I went to a > LLMD > > in New Jersey was I diagnosed with Lyme and co-infections. So I suggest > > getting checked for co-infections also, for that too can create a whole > > bunch of other problems. > > Good luck to your friend in this journey.... > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 19, 2009 Report Share Posted November 19, 2009 Hi , The other day I spoke to her husband. They were still working on pain control for but otherwise she was doing great. She is not answering her cell so I haven't been able to speak with her directly. I read you had a date! Wow! After all this time .... You will do fine after all, he is one of the best. C > > Hi C - > Any more news on ?? I'm anxious to hear how things are going? Also, as you have probably read by now, I've seen Dr. Glazer again and have a revision date of March 15! > D (RI) > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 20, 2009 Report Share Posted November 20, 2009 Yes, he is one of the best!! And I'm delighted and humbled to be in such great hands. I recently spoke with Joanne Chertok - she had her surgery with Glazer almost 5 years ago and she told me that she has been painfree for almost as long and doing great too! She said he gave her a whole new lease on life and she couldn't be better!! Got to love it! He sure has an excess of success stories and I plan on being one of them too!! D (RI) > > > > Hi C - > > Any more news on ?? I'm anxious to hear how things are going? Also, as you have probably read by now, I've seen Dr. Glazer again and have a revision date of March 15! > > D (RI) > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2010 Report Share Posted January 25, 2010 Hello! any person who has had Dr. Aceves for your wls live in the Panama City Florida area? We just moved here from Las Vegas where we were living at the time of my band. joanne Re: At Lucerna I live in Yuma about 1hr and 1/2 from Mexicali and it is really bad for us. My pool is flooded over along with all the roads. The winds are up to almost 100 miles an hour. And it is still going I have lived in Arizona for 3yrs now and never seen anything like this before.>> Did you all see the big storm over Mexicali today? http://radar.weather.gov/radar.php?product=N0R & rid=yux & loop=yes> > Marilou> Dr. Aceves> VSG~February 5, 2010> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ________________________________ From: yp_julie_braintree <julieat575@...> Hepatitis C Sent: Sat, March 13, 2010 11:38:30 AM Subject: ?  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 It's not a curse, and you're not alone. There's lots of interesting information on this web site. CDC has information. What have you done yet? J From: yp_julie_braintree <julieat575@...> Subject: ? Hepatitis C Date: Saturday, March 13, 2010, 11:38 AM  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 I've been take some " natural supplement " antioxidants and other herbs, never have felt sick and can't afford the expensive the internist want to put me on. Jackie From: Sheri Sheeder <sherisheeder@...> Subject: Re: ? Hepatitis C Date: Saturday, March 13, 2010, 5:00 PM  Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ____________ _________ _________ __ From: yp_julie_braintree <julieat575 (DOT) com> Hepatitis Csupportgr oupgroups (DOT) com Sent: Sat, March 13, 2010 11:38:30 AM Subject: ?  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 Yes there are many of us out here for u. It's not a curse. In a way it's been a blessing as I have appreciated every day more since I was diagnosed 30 years ago last month. Do all the things u enjoy but put off starting tomorrow, fulfill every desire within measure, do something kind for someone every day, adopt a cat or dog from The SPCA, help those who are old or infirmed worse than u. Believe me, u will feel better about your own condition and it will come back to you. It's the pay it forward thoughts.  Patti From: yp_julie_braintree <julieat575@...> Subject: ? Hepatitis C Date: Saturday, March 13, 2010, 11:38 AM  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 I'm getting my medicines through the pegassist program, it's through the company that make the stuff, Roche. But to apply for help you have to go to the pegassist website, they also have alot of information on there as well. For the past couple of years the dr's couldn't figure out why I was always under the weather, most the time they said they couldn't find anything wrong and that I must just have a cold or be over doing it and getting wore out and it's just my body telling me to slow down and sleep more. Then nine months ago a dr. ran a bunch of test during a follow up visit after I had a mini stroke and noticed that my liver count was high so he ran the hep test and it was positive, so I've been seeing a liver specialist ever since. I have never used IV drugs and the best we can come up with is that I got it 25yrs ago when I was given blood after my youngest daughter was born. They don't usually test for hepititis unless they think you have it and that's why I wasn't diagnosed earlier. Have a goodnight everyone. Sheri ________________________________ From: Jackie Ware <bchgirl49@...> Hepatitis C Sent: Sat, March 13, 2010 5:35:53 PM Subject: Re: ?  I've been take some " natural supplement " antioxidants and other herbs, never have felt sick and can't afford the expensive the internist want to put me on. Jackie From: Sheri Sheeder <sherisheeder@ ymail.com> Subject: Re: ? Hepatitis Csupportgr oupgroups (DOT) com Date: Saturday, March 13, 2010, 5:00 PM  Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ____________ _________ _________ __ From: yp_julie_braintree <julieat575@ . com> Hepatitis Csupportgr oupgroups (DOT) com Sent: Sat, March 13, 2010 11:38:30 AM Subject: ?  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 hi,im only 34 and i have all this medical problem.my doctor just told me that i have hep c im scare i dont know what to do its been like a month an im still waiting for the medicine to come thew.i know that everything will be ok. ________________________________ From: Sheri Sheeder <sherisheeder@...> Hepatitis C Sent: Sat, March 13, 2010 6:00:04 PM Subject: Re: ?  Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ____________ _________ _________ __ From: yp_julie_braintree <julieat575 (DOT) com> Hepatitis Csupportgr oupgroups (DOT) com Sent: Sat, March 13, 2010 11:38:30 AM Subject: ?  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 ________________________________ From: Sheri Sheeder <sherisheeder@...> Hepatitis C Sent: Sat, March 13, 2010 6:00:04 PM Subject: Re: ? Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ____________ _________ _________ __ From: yp_julie_braintree <julieat575 (DOT) com> Hepatitis Csupportgr oupgroups (DOT) com Sent: Sat, March 13, 2010 11:38:30 AM Subject: ? 1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 14, 2010 Report Share Posted March 14, 2010 Let me know how the pegasys works. That was one of my concerns as I didn't think I would be able to continue work, I'm 60, and live by myself. Jackie From: Sheri Sheeder <sherisheeder@ ymail.com> Subject: Re: ? Hepatitis Csupportgr oupgroups (DOT) com Date: Saturday, March 13, 2010, 5:00 PM  Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ____________ _________ _________ __ From: yp_julie_braintree <julieat575@ . com> Hepatitis Csupportgr oupgroups (DOT) com Sent: Sat, March 13, 2010 11:38:30 AM Subject: ?  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 14, 2010 Report Share Posted March 14, 2010 I will let everyone know how I'm doing, I'm thinking about getting a lap top so if I have days were I'm sick in bed I can still play on the computer. My boyfriend says I will be in bed to rest not play on facebook. Lol. I'm there alot so come find me if you like, I'm the only one listed as Sheri Sheeder, and I would love the company. Sheri ________________________________ From: Jackie Ware <bchgirl49@...> Hepatitis C Sent: Sun, March 14, 2010 11:08:30 AM Subject: Re: ?  Let me know how the pegasys works. That was one of my concerns as I didn't think I would be able to continue work, I'm 60, and live by myself. Jackie From: Sheri Sheeder <sherisheeder@ ymail.com> Subject: Re: ? Hepatitis Csupportgr oupgroups (DOT) com Date: Saturday, March 13, 2010, 5:00 PM  Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ____________ _________ _________ __ From: yp_julie_braintree <julieat575@ . com> Hepatitis Csupportgr oupgroups (DOT) com Sent: Sat, March 13, 2010 11:38:30 AM Subject: ?  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 15, 2010 Report Share Posted March 15, 2010 Sheri, please keep me posted on how the medicine works for you and you're in my thoughts. Jackie From: Sheri Sheeder <sherisheeder@ ymail.com> Subject: Re: ? Hepatitis Csupportgr oupgroups (DOT) com Date: Saturday, March 13, 2010, 5:00 PM  Your in the right place. Everyone in here is very helpful. Your not alone. I found out about 9mo. ago and still have my days of denial but my not feeling good all the time brings me back to the world to. I'm getting ready to start treatment anytime, just waiting for the medicines to arrive. I have a dr. app. on tuesday to get some shots for other stuff and sign some more papers. I scared, no I'm petrified but I figure that I'm sick all the time now and if this works it will be worth it. Don't ever be afraid to ask a question in here, as a matter of fact ask alot of them, if someone don't already know the answer they will help you find it. Sheri ____________ _________ _________ __ From: yp_julie_braintree <julieat575@ . com> Hepatitis Csupportgr oupgroups (DOT) com Sent: Sat, March 13, 2010 11:38:30 AM Subject: ?  1st time texter! I have learned 2 yrs. ago I have the curse. I'm in denial. I need some help here Quote Link to comment Share on other sites More sharing options...
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