Guest guest Posted May 18, 2008 Report Share Posted May 18, 2008 Hello all, As a follow up to Message (Walk for LDN Awareness - Please e-mail the Governor!! ), I corresponded with Sammy Jo about Vicki's News Coverage and her response was "Vicki said the local TV news is meeting her, but if you have #'s for the major TV news that is a great idea! Post away!"......so let's Post away and send e-mails to the local Sacramento stations, asking them to cover Vicki both at the local and National levels. Since this is such a great story, please ask the local affiliates to also send the story to the national affiliate. I've included links to the major stations below. Additionally, I included an example of what I already sent - feel free to copy/paste/modify and include how LDN has helped you in your disease (cancer, AutoImmune, HIV/AIDS, Autism, etc.). The more people that send in their stories of success with LDN, the more likely the news stations are to cover this story and/or send it to the national level. Please also send an e-mail to the Governor, if you have not done so already (see the Message above for a link to his e-mail). Everything that we can do to get LDN in the news leads us one step closer to clinical trials in each of our diseases! Vicki is an inspiration on what one person can do to further the LDN cause. And we, too, can be a part of her support by e-mailing the news media and telling them about Vicki and our stories. Thanks! *************News Media in Sacramento ************** http://fox40.trb.com/news/ktxl-viewers-voice-new-2,0,5945421.customform (FOX Sacramento) http://www.kcra.com/news/1675042/detail.html (NBC Sacramento) http://www.sacramentotop10.com/Entertainment/KMAX-TV-Sacramento.php (CBS Sacramento) http://www.news10.net/company/contact/contact.aspx (ABC Sacramento) http://www.sacramentotop10.com/Entertainment/Television.html (Sacramento TV Stations) http://www.mondotimes.com/1/world/us/5/309 (Sacramento News Media) **************** Hello, I have a news item that I believe would be of great interest to both your local and national viewers. This news story is currently happening in the Sacramento area and will culminate at 2:00 at the Capital Steps in Sacramento on Monday, May 19th, where Vicki Finlayson hopes to meet with Governor Schwarzenegger. It's a ' versus Goliath' story of Vicki Finlayson versus Multiple Sclerosis. It is a personal interest story of Vicki's courage and determination in finding Low Dose Naltrexone (LDN), the drug that has made walking & normal life possible again for her. But it is also a & Goliath story of the current Big Pharmaceutical Giants against a low cost, generic drug that can help so many conditions where the immune system is not properly functioning. Besides MS, LDN is also being used successfully in many AutoImmune, Cancer, HIV/AIDS, Autism, Viral Diseases, and other conditions by thousands of patients, but few patients have heard of it. LDN's promotion has become a grass roots efforts, lead by many people, including Vicki's efforts. Naltrexone is an opioid antagonist and already approved by the FDA for other conditions such as drug and alcohol addition. Naltrexone has also been proven (by NIH and other researchers) over the past few years to also offer great benefits to the immune system in multiple diseases when used in very minimal dosages. The University of Pennsylvania (Hershey Medical School, Dr. Ian Zagon, Dr. Jill , and others have been doing significant medical research into this area for years. Last year, a LDN Crohn's Study was released where 89% showed improvement in their condition and 69% of the Crohn's patients went into remission (and this at the cost of approximately $1.00 a day -- yes...that's 100 pennies)! Regular dose Naltrexone was already FDA approved many years ago, and is now in the generic stage where it is so cheap. LDN must be compounded to make it approximately 1/10 to 1/15 of the regular dosage of Naltrexone. Therefore, there is no profit in any drug company doing any of the clinical studies for LDN for any medical condition since it can already be used in an 'off-label' use. That means that most clinical studies specific to LDN are or will be either sponsored by the Government (such as National Institutes of Health, NIH) or groups personally raising funds to sponsor a study, such as Vicki. We, ourselves, have seen the power of LDN in my daughter's liver condition. While we were waiting for a pediatric liver trial to start for my daughter's condition, we found LDN. LDN made an immediate impact in the condition of her liver and she has made significant improvement (and no longer needs any liver drugs). LDN cost us $20 a month, instead of the approximate $800/month for the other drug she would have taken. That's a significant health savings, as well as the dramatic improvement in her liver condition!! Please talk to Vicki and hear her inspiring story. Please also learn about this very inspiring drug, LDN, that is already FDA approved and may be prescribed 'off-label' for these other conditions. For more information on Vicki, please see http://www.ldners.org/advocates.htm. http://www.sacbee.com/health/story/939531.html. Also, for more information on LDN, please see http://www.ldninfo.org/ . For more information about Dr. Ian Zagon and his work on how opioid antagonists (such as LDN) influence the immune system, please see http://fred.psu.edu/ds/retrieve/fred/investigator/isz1 I think this story would be of interest to the national community, as well as the local community. Would you please pass this on to your national affiliate? Thank you! *********************************** Three Cheers for Vicki! >> > > Please support her by sending an email to Gov Schwarzenegger. Tell> him the importance of LDN research. Tell your LDN story. I have a link> to his office at http://www.ldners.org/advocates.htm> <http://www.ldners.org/advocates.htm>> > > Hi all,> > First, thanks to Sammy Jo for posting this great news! This is an> opportunity for all of those on this Group to easily make a> positive impact!! Vicki (as an Multiple Sclerosis patient) is walking> 53 miles to raise LDN awareness and funds! Now that's dediction and> determination to put LDN on the map. For more information on Vicki,> please see http://www.ldners.org/advocates.htm> <http://www.ldners.org/advocates.htm> . Also, I would encourage you to> send the Governor an e-mail. Anything that we can do to get LDN in the> news, realistically moves us one step closer towards clinical studies> for each of our diseases. So let's please support Vicki in her efforts!> Please Send Governor Schwarzenegger an email> <http://gov.ca.gov/interact#email> and tell him to meet with Vicki!> > I sent the below e-mail tonight to him (if you want to copy/paste> parts of my e-mail, feel free to)!> > Go Vicki - And "Thank YOU!" on behalf of us, our children, family> members, and all of those who suffer and have/will in the future benefit> from LDN! You have our respect, prayers, and best regards!> > Cheers ~ Joyce> > > > Dear Governator (Mr. Schwarzenegger),> > > > You, as the Governor, have an opportunity to reduce your Health> care costs in California and be an innovator for the U.S. Yes - you can> effect change!! Vicki Finlayson, who suffers from Multiple Sclerosis> (MS) has an incredible story on how she has been helped by Low Dose> Naltrexone (also known as LDN). She is walking to the Capitol steps in> Sacramento on May 19th at 2pm and hopes to meet with you in order to> raise awareness of this very low cost drug. LDN is a very Low Dose of> Naltrexone. Naltrexone, which is an opioid antagonist, has been proven> (by NIH and other researchers) over the past few years to modulate the> immune system in multiple diseases. The University of Pennsylvania> (Hershey Medical School, Dr. Ian Zagon, Dr. Jill , and others have> been doing significant medical research into this area for years. Last> year, a LDN Crohn's Study was released where 89% showed improvement in> their condition and 69% of the Crohn's patients went into remission (and> this at the cost of approximately $1.00 a day -- yes...that's 100> pennies)!> > > > Regular dose Naltrexone was already FDA approved many years ago,> and is now in the generic stage where it is so cheap. LDN must be> compounded to make it approximately 1/10 to 1/15 of the regular dosage> of Naltrexone. Therefore, there is no profit in any drug company doing> any of the clinical studies for LDN for any medical condition since it> can already be used in an 'off-label' use. That means that most> clinical studies specific to LDN are or will be either sponsored by the> Government (such as National Institutes of Health, NIH) or groups> personally raising funds to sponsor a study, such as Vicki.> > > > We, ourselves, have seen the power of LDN in my daughter's liver> condition. While we were waiting for a pediatric liver trial to start> for my daughter's condition, we found LDN. LDN made an immediate> impact in the condition of her liver and she has made significant> improvement (and no longer needs any liver drugs). LDN cost us $20 a> month, instead of the approximate $800/month for the other drug she> would have taken. That's a significant health savings, as well as the> dramatic improvement in her liver condition!!> > > > So please meet with Vicki and learn how you can make health care> affordable for California. Please set an example of innovative> approaches to health care. For more information on Vicki, please read> (> http://www.auburnjournal.com/detail/51371.html?content_source=archive). > For more information on LDN, please read http://www.ldninfo.org/. > Thanks!> > > > Sincerely, Joyce> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 18, 2008 Report Share Posted May 18, 2008 dudley_delany [LDN_Users] Vicki & LDN - Please E-Mail News Media for Coverage & Governor Hello all, As a follow up to Message (LDN Awareness Walk - Please E-Mail Gov. Schwarzenegger <LDN_Users/message/5955> ), I corresponded with Sammy Jo about Vicki's News Coverage and her response was " Vicki said the local TV news is meeting her, but if you have #'s for the major TV news that is a great idea! Post away! " ......so let's Post away and send e-mails to the local Sacramento stations, asking them to cover Vicki both at the local and National levels. Since this is such a great story, please ask the local affiliates to also send the story to the national affiliate. I've included links to the major stations below. Additionally, I included an example of what I already sent - feel free to copy/paste/modify and include how LDN has helped you in your disease (cancer, AutoImmune, HIV/AIDS, Autism, etc.). The more people that send in their stories of success with LDN, the more likely the news stations are to cover this story and/or send it to the national level. Please also send an e-mail to the Governor, if you have not done so already (see the Message above for a link to his e-mail). Everything that we can do to get LDN in the news leads us one step closer to clinical trials in each of our diseases! Vicki is an inspiration on what one person can do to further the LDN cause. And we, too, can be a part of her support by e-mailing the news media and telling them about Vicki and our stories. Thanks! *************News Media in Sacramento ************** http://fox40.trb.com/news/ktxl-viewers-voice-new-2,0,5945421.customform <http://fox40.trb.com/news/ktxl-viewers-voice-new-2,0,5945421.customform\ > (FOX Sacramento) http://www.kcra.com/news/1675042/detail.html <http://www.kcra.com/news/1675042/detail.html> (NBC Sacramento) http://www.sacramentotop10.com/Entertainment/KMAX-TV-Sacramento.php <http://www.sacramentotop10.com/Entertainment/KMAX-TV-Sacramento.php> (CBS Sacramento) http://www.news10.net/company/contact/contact.aspx <http://www.news10.net/company/contact/contact.aspx> (ABC Sacramento) http://www.sacramentotop10.com/Entertainment/Television.html <http://www.sacramentotop10.com/Entertainment/Television.html> (Sacramento TV Stations) http://www.mondotimes.com/1/world/us/5/309 <http://www.mondotimes.com/1/world/us/5/309> (Sacramento News Media) **************** Hello, I have a news item that I believe would be of great interest to both your local and national viewers. This news story is currently happening in the Sacramento area and will culminate at 2:00 at the Capital Steps in Sacramento on Monday, May 19th, where Vicki Finlayson hopes to meet with Governor Schwarzenegger. It's a ' versus Goliath' story of Vicki Finlayson versus Multiple Sclerosis. It is a personal interest story of Vicki's courage and determination in finding Low Dose Naltrexone (LDN), the drug that has made walking & normal life possible again for her. But it is also a & Goliath story of a low cost, generic drug that can help so many conditions where the immune system is not properly functioning versus Big Pharmaceutical Giants. Besides MS, LDN is also being used successfully in many AutoImmune, Cancer, HIV/AIDS, Autism, Viral Diseases, and other conditions by thousands of patients, but few patients have heard of it. LDN's promotion has become a grass roots effort, lead by many people, including Vicki. Naltrexone is an opioid antagonist and already approved by the FDA for other conditions such as drug and alcohol addition. Naltrexone has also been proven (by NIH and other researchers) over the past few years to also offer great benefits to the immune system in multiple diseases when used in very minimal dosages. The University of Pennsylvania (Hershey Medical School, Dr. Ian Zagon, Dr. Jill , and others have been doing significant medical research into this area for years. Last year, a LDN Crohn's Study was released where 89% showed improvement in their condition and 69% of the Crohn's patients went into remission (and this at the cost of approximately $1.00 a day -- yes...that's 100 pennies)! Regular dose Naltrexone was already FDA approved many years ago, and is now in the generic stage where it is so cheap. LDN must be compounded to make it approximately 1/10 to 1/15 of the regular dosage of Naltrexone. Therefore, there is no profit in any drug company doing any of the clinical studies for LDN for any medical condition since it can already be used in an 'off-label' use. That means that most clinical studies specific to LDN are or will be either sponsored by the Government (such as National Institutes of Health, NIH) or groups personally raising funds to sponsor a study, such as Vicki. We, ourselves, have seen the power of LDN in my daughter's liver condition. While we were waiting for a pediatric liver trial to start for my daughter's condition, we found LDN. LDN made an immediate impact in the condition of her liver and she has made significant improvement (and no longer needs any liver drugs). LDN cost us $20 a month, instead of the approximate $800/month for the other drug she would have taken. That's a significant health savings, as well as the dramatic improvement in her liver condition!! Please talk to Vicki and hear her inspiring story. Please also learn about this very inspiring drug, LDN, that is already FDA approved and may be prescribed 'off-label' for these other conditions. For more information on Vicki, please see http://www.ldners.org/advocates.htm <http://www.ldners.org/advocates.htm> . http://www.sacbee.com/health/story/939531.html <http://www.sacbee.com/health/story/939531.html> . Also, for more information on LDN, please see http://www.ldninfo.org/ <http://www.ldninfo.org/> . For more information about Dr. Ian Zagon and his work on how opioid antagonists (such as LDN) influence the immune system, please see http://fred.psu.edu/ds/retrieve/fred/investigator/isz1 <http://fred.psu.edu/ds/retrieve/fred/investigator/isz1> I think this story would be of interest to the national community, as well as the local community. Would you please pass this on to your national affiliate? Thank you! *********************************** Three Cheers for Vicki! > > > Hi all, > > Sammy Jo passed on the below Message (at the bottom of this post) > about Vicki Finlayson's walk to raise LDN awareness. We have an > opportunity for all of on this Group to easily make a positive > impact!! Vicki (as an Multiple Sclerosis patient) is walking 53 miles > to raise LDN awareness and funds! Now that's dediction and > determination to put LDN on the map. For more information on Vicki, > please see http://www.ldners.org/advocates.htm > <http://www.ldners.org/advocates.htm> . Also, I would encourage you to > send the Governor an e-mail. Anything that we can do to get LDN in the > news, realistically moves us one step closer towards clinical studies > for each of our diseases. So let's please support Vicki in her efforts! > Please Send Governor Schwarzenegger an email > <http://gov.ca.gov/interact#email> and tell him to meet with Vicki! > > I sent the below e-mail tonight to him (if you want to copy/paste > parts of my e-mail, feel free to)! > > Go Vicki - And " Thank YOU! " on behalf of us, our children, family > members, and all of those who suffer and have/will in the future benefit > from LDN! You have our respect, prayers, and best regards! > > Cheers ~ Joyce > > > > Dear Governator (Mr. Schwarzenegger), > > > > You, as the Governor, have an opportunity to reduce your Health > care costs in California and be an innovator for the U.S. Yes - you can > effect change!! Vicki Finlayson, who suffers from Multiple Sclerosis > (MS) has an incredible story on how she has been helped by Low Dose > Naltrexone (also known as LDN). She is walking to the Capitol steps in > Sacramento on May 19th at 2pm and hopes to meet with you in order to > raise awareness of this very low cost drug. LDN is a very Low Dose of > Naltrexone. Naltrexone, which is an opioid antagonist, has been proven > (by NIH and other researchers) over the past few years to modulate the > immune system in multiple diseases. The University of Pennsylvania > (Hershey Medical School, Dr. Ian Zagon, Dr. Jill , and others have > been doing significant medical research into this area for years. Last > year, a LDN Crohn's Study was released where 89% showed improvement in > their condition and 69% of the Crohn's patients went into remission (and > this at the cost of approximately $1.00 a day -- yes...that's 100 > pennies)! > > > > Regular dose Naltrexone was already FDA approved many years ago, > and is now in the generic stage where it is so cheap. LDN must be > compounded to make it approximately 1/10 to 1/15 of the regular dosage > of Naltrexone. Therefore, there is no profit in any drug company doing > any of the clinical studies for LDN for any medical condition since it > can already be used in an 'off-label' use. That means that most > clinical studies specific to LDN are or will be either sponsored by the > Government (such as National Institutes of Health, NIH) or groups > personally raising funds to sponsor a study, such as Vicki. > > > > We, ourselves, have seen the power of LDN in my daughter's liver > condition. While we were waiting for a pediatric liver trial to start > for my daughter's condition, we found LDN. LDN made an immediate > impact in the condition of her liver and she has made significant > improvement (and no longer needs any liver drugs). LDN cost us $20 a > month, instead of the approximate $800/month for the other drug she > would have taken. That's a significant health savings, as well as the > dramatic improvement in her liver condition!! > > > > So please meet with Vicki and learn how you can make health care > affordable for California. Please set an example of innovative > approaches to health care. For more information on Vicki, please read > ( > http://www.auburnjournal.com/detail/51371.html?content_source=archive). > For more information on LDN, please read http://www.ldninfo.org/. > Thanks! > > > > Sincerely, ....... > > > > Sammy Jo's Note Below - I have her permission to share this with the > different LDN Groups.... > > Vicki just called me at Mile 6 of 53! > > She was on Hwy 49, I could hear the cars wooshing by. > > Please support her by sending an email to Gov Schwarzenegger. > Tell him the importance of LDN research. Tell your LDN story. > > I have a link to his office at http://www.ldners.org/advocates.htm > <http://www.ldners.org/advocates.htm> > > Vicki wants him to meet her at the Capitol on Monday. > > SammyJo > Quote Link to comment Share on other sites More sharing options...
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