National Health Funding for Low Dose Naltrexone in Australia Petition: Signature List Feed http://www.gopetition.com/signatures/national-health-funding-for-low-dose-naltrexone-in-australia.html Online petition signatures en-us Tue, 7 Apr 2026 06:02 UTC GoPetition RSS Feed Generator Copyright 2026 GoPetition Ms Elaine Kelly [Signature #199] https://www.gopetition.com/signature/locate/12388186?utm_medium=rss LDN is of benefit to many people with chronic illnesses for pain relief and immune modification. The current expense and lack of availability makes using it prohibitive to those who need it most.

]]> Fri, 16 Mar 2012 04:22:54 UTC 12388186 Ms Denise Testa [Signature #198] https://www.gopetition.com/signature/locate/12384251?utm_medium=rss Not just cancer etc, don't forget those with sarcoidosis and chronic lyme.

]]> Fri, 16 Mar 2012 12:11:51 UTC 12384251 Ms Sue Sherratt [Signature #197] https://www.gopetition.com/signature/locate/12383017?utm_medium=rss I'm currently taking for Sarcoidosis and amazed how it's reduced my pain levels to the point that nearly all my pain meds have been stopped.

]]> Thu, 15 Mar 2012 07:35:27 UTC 12383017 Mrs elizabeth baxter [Signature #196] https://www.gopetition.com/signature/locate/11951164?utm_medium=rss Fri, 6 Jan 2012 09:01:08 UTC 11951164 Ms Judy D [Signature #195] https://www.gopetition.com/signature/locate/11950964?utm_medium=rss People who benefit most from this drug are the least able to afford it. It makes the difference between being able to work or not work. That is a benefit to the individual, their family and the Govt.

]]> Fri, 6 Jan 2012 07:48:11 UTC 11950964 Mrs Anonymous [Signature #194] https://www.gopetition.com/signature/locate/11917991?utm_medium=rss It should be free

]]> Sat, 31 Dec 2011 05:24:32 UTC 11917991 ms Anonymous [Signature #193] https://www.gopetition.com/signature/locate/11897836?utm_medium=rss Sun, 25 Dec 2011 04:35:04 UTC 11897836 Mrs Emily stock [Signature #192] https://www.gopetition.com/signature/locate/11895260?utm_medium=rss Fri, 23 Dec 2011 10:35:50 UTC 11895260 Ms Andrea Treloar [Signature #191] https://www.gopetition.com/signature/locate/11894004?utm_medium=rss Fri, 23 Dec 2011 01:07:37 UTC 11894004 ms kate siciliano [Signature #190] https://www.gopetition.com/signature/locate/11893008?utm_medium=rss Fri, 23 Dec 2011 07:03:55 UTC 11893008 Mrs Caroline Blake [Signature #189] https://www.gopetition.com/signature/locate/11892976?utm_medium=rss Fri, 23 Dec 2011 06:51:24 UTC 11892976 Mrs Caroline Bailey [Signature #188] https://www.gopetition.com/signature/locate/11892904?utm_medium=rss On behalf of my family, I appeal the Australian Government to make this drug easily accessible for Australians suffering these crippling diseases. My husband has MS and we have 3 young children. We miss out on so much - please help us!

]]> Fri, 23 Dec 2011 06:20:23 UTC 11892904 Ms Kerry Boyne [Signature #187] https://www.gopetition.com/signature/locate/11516126?utm_medium=rss Mon, 14 Nov 2011 10:34:21 UTC 11516126 Ms Nielle Hartmann [Signature #186] https://www.gopetition.com/signature/locate/11484555?utm_medium=rss Wed, 9 Nov 2011 08:17:11 UTC 11484555 Miss Jodie Newman [Signature #185] https://www.gopetition.com/signature/locate/11484515?utm_medium=rss I am currently taking LDN for ME/CFS (despite the high stigma attached to this condition, I managed to find a doctor willing to help me, by allowing me to trial this medication). I have encountered undeniable benefits whilst in use of Low Dose Naltrexone and am appalled that so many people are needlessly suffering, when this could be an amazing aid in the management of their condition. I implore you to take this petition with the serious stance it deserves.

]]> Wed, 9 Nov 2011 08:07:35 UTC 11484515 Mr Anonymous [Signature #184] https://www.gopetition.com/signature/locate/11454279?utm_medium=rss Sat, 5 Nov 2011 12:49:09 UTC 11454279 Ms Anonymous [Signature #183] https://www.gopetition.com/signature/locate/11383690?utm_medium=rss I or anyone already suffering debilitating illnesses such as the wide list of what this medication can possibly target will end up on a pension if not already, would make sense to fund this and keep people healthier for longer and may even stop some from needing a pension at all, I have suffered from CFS, for many years and recently diagnosed with RA, I am bedridden alot. I would like to try LDN, the cost is harsh.

]]> Sun, 23 Oct 2011 09:03:51 UTC 11383690 Ms Anonymous [Signature #182] https://www.gopetition.com/signature/locate/10912134?utm_medium=rss Tue, 26 Jul 2011 07:54:02 UTC 10912134 Ms Anonymous [Signature #181] https://www.gopetition.com/signature/locate/10892934?utm_medium=rss LDN is a cheap and seemingly effective health improvement agent so lets get behind it.

]]> Fri, 22 Jul 2011 02:47:25 UTC 10892934 Ms Jacqui Foster [Signature #180] https://www.gopetition.com/signature/locate/10888272?utm_medium=rss Thu, 21 Jul 2011 07:00:36 UTC 10888272 ms Anonymous [Signature #179] https://www.gopetition.com/signature/locate/10673422?utm_medium=rss we want doctors to prescribe it so we can be tested and have results and follow ups as taking it willy nilly we don't know if it's working or not just hope it is ! seems hopeful

]]> Tue, 14 Jun 2011 05:01:52 UTC 10673422 mrs ann pell [Signature #178] https://www.gopetition.com/signature/locate/10499340?utm_medium=rss Fri, 20 May 2011 04:53:41 UTC 10499340 Ms Karen Cooke [Signature #177] https://www.gopetition.com/signature/locate/10486412?utm_medium=rss Please give this low-cost and low risk treatment to those of us who need it. Make it affordable and make it happen fast. Help ease our pain and our fears. It should be available to all with progressive diseases, pain and others where not contraindicated. LDN doesn't seem to have any problems associated with it esp when compared to interferons, morhine, heroin, alcohol, marijuana, cigarettes and whatever else people are given or self administer. Investigate and supply!!! As soon as possible!

]]> Wed, 18 May 2011 08:36:12 UTC 10486412 Ms Anonymous [Signature #176] https://www.gopetition.com/signature/locate/10453500?utm_medium=rss Fri, 13 May 2011 10:33:50 UTC 10453500 Mr Martin Sawtell [Signature #175] https://www.gopetition.com/signature/locate/10092962?utm_medium=rss Mon, 28 Mar 2011 03:22:28 UTC 10092962 Mrs Anonymous [Signature #174] https://www.gopetition.com/signature/locate/10077307?utm_medium=rss Sat, 26 Mar 2011 06:51:35 UTC 10077307 Mr Anonymous [Signature #173] https://www.gopetition.com/signature/locate/10051284?utm_medium=rss Tue, 22 Mar 2011 10:08:25 UTC 10051284 Mr Peter Lucas [Signature #172] https://www.gopetition.com/signature/locate/10032656?utm_medium=rss get behind this people,

]]> Sun, 20 Mar 2011 09:20:18 UTC 10032656 mrs margo lucas [Signature #171] https://www.gopetition.com/signature/locate/10032614?utm_medium=rss i am in remission with her2 positive breast cancer..i have a husband and 2 still dependant children and i want to live to see them grow up..please make LDN available to us who need it..its a matter of survival for some of us ..thankyou xxx

]]> Sun, 20 Mar 2011 09:03:23 UTC 10032614 Ms Fiona Astridge [Signature #170] https://www.gopetition.com/signature/locate/10027322?utm_medium=rss Sun, 20 Mar 2011 01:06:22 UTC 10027322 Ms Liz Biltoft [Signature #169] https://www.gopetition.com/signature/locate/9775123?utm_medium=rss Fri, 25 Feb 2011 07:41:15 UTC 9775123 mr don McMaster [Signature #168] https://www.gopetition.com/signature/locate/9492607?utm_medium=rss I would like to try this drug but it seems hard to get a script

]]> Thu, 3 Feb 2011 04:11:13 UTC 9492607 Ms Jacqueline Chay [Signature #167] https://www.gopetition.com/signature/locate/9321338?utm_medium=rss LDN may be helpful for Hasimoto's autoimmune disease, and I should have the chance to try it.

]]> Mon, 17 Jan 2011 12:04:44 UTC 9321338 Ms Angelica Rodriguez [Signature #166] https://www.gopetition.com/signature/locate/9124822?utm_medium=rss Sat, 18 Dec 2010 08:06:49 UTC 9124822 mr damian musulin [Signature #165] https://www.gopetition.com/signature/locate/8973679?utm_medium=rss Tue, 23 Nov 2010 12:59:21 UTC 8973679 Ms Mary Lusted [Signature #164] https://www.gopetition.com/signature/locate/8786949?utm_medium=rss Wed, 27 Oct 2010 11:02:57 UTC 8786949 Ms Anonymous [Signature #163] https://www.gopetition.com/signature/locate/8773070?utm_medium=rss We need to have Low Dose Naltrexone available in Australia, to help the many people whose lives have been afflicted by disease.

]]> Sun, 24 Oct 2010 11:25:39 UTC 8773070 Mrs Beth Carter [Signature #162] https://www.gopetition.com/signature/locate/8735349?utm_medium=rss Sun, 17 Oct 2010 07:36:16 UTC 8735349 Mrs Anonymous [Signature #161] https://www.gopetition.com/signature/locate/8674849?utm_medium=rss Sat, 9 Oct 2010 04:54:02 UTC 8674849 Ms Helen Ganatsios [Signature #160] https://www.gopetition.com/signature/locate/8642919?utm_medium=rss Please,, please ,, to those in goverment please hear our cries for help , make LDN readily available in Australia for all of us that are suffering from chronic & disabiling diseases ,,, it will help our economy vastly & we will be much happier people for it.

]]> Tue, 5 Oct 2010 11:09:34 UTC 8642919 Mrs Leoni Nicholson [Signature #159] https://www.gopetition.com/signature/locate/8447237?utm_medium=rss Sun, 5 Sep 2010 11:33:53 UTC 8447237 Ms Irene Brace [Signature #158] https://www.gopetition.com/signature/locate/8354030?utm_medium=rss Fund research for LDN, my husband and daughter is STRICKENED with Crohn's disease and Arthritis, along with other members of the family.

]]> Fri, 20 Aug 2010 12:28:48 UTC 8354030 Ms Angela Sather [Signature #157] https://www.gopetition.com/signature/locate/8353596?utm_medium=rss Fri, 20 Aug 2010 10:35:14 UTC 8353596 Ms Leonie Hitchenor [Signature #156] https://www.gopetition.com/signature/locate/8241865?utm_medium=rss I suffer from FM as well as Hashimotos, I am disabled by pain & illness with no hope of a cure, this may help me & thousands of others like me to live a normal productive life again, please help.

]]> Thu, 29 Jul 2010 09:50:17 UTC 8241865 Mr Dean McNair [Signature #155] https://www.gopetition.com/signature/locate/7978116?utm_medium=rss Sun, 20 Jun 2010 10:10:54 UTC 7978116 Mr Rohan Erm [Signature #154] https://www.gopetition.com/signature/locate/7888103?utm_medium=rss Mon, 7 Jun 2010 11:39:01 UTC 7888103 mrs maree willcox [Signature #153] https://www.gopetition.com/signature/locate/7788363?utm_medium=rss Sat, 29 May 2010 01:46:34 UTC 7788363 Mrs Amanda Galligan [Signature #152] https://www.gopetition.com/signature/locate/7478284?utm_medium=rss The Australian Govnt must get behind this request for LDN to be allowed to be used. I was diagnosed 2007 with MS. I am getting worse which is going to do my head in. We need help.

]]> Fri, 30 Apr 2010 02:19:10 UTC 7478284 m r john vinton [Signature #151] https://www.gopetition.com/signature/locate/7383377?utm_medium=rss why is information being with held in australia about ldn.went to see doctor about a prescription for ldn i may as well have asked him to hold a black snake. he could not spell the name let alone priscribe it.,and i am sure any fibromyalga sufferer knows what comes next.ITS ALL IN YOUR HEAD ,TAKE SOME LYICRA(ANTIDEPRESSANT)
oh and we will THROW in some statins LIPITOR and lipodill and dont forget the betta blockers. all poisons.but what a about NALTREXONE!!!.WHATS THAT!!!!!!!
KNOW PROFIT

]]> Wed, 14 Apr 2010 10:50:19 UTC 7383377 Ms Deborah Shaw [Signature #150] https://www.gopetition.com/signature/locate/7381202?utm_medium=rss I suffer with Fibromyalgia and would like options and education for GP's.

]]> Wed, 14 Apr 2010 06:15:07 UTC 7381202 Ms Crystal Nason [Signature #149] https://www.gopetition.com/signature/locate/7303220?utm_medium=rss Wed, 7 Apr 2010 06:07:16 UTC 7303220 Mr simon seawright [Signature #148] https://www.gopetition.com/signature/locate/7303107?utm_medium=rss Wed, 7 Apr 2010 05:40:36 UTC 7303107 Ms elle elan [Signature #147] https://www.gopetition.com/signature/locate/7243933?utm_medium=rss Sat, 27 Mar 2010 10:04:00 UTC 7243933 Ms Raewyn Pilkington [Signature #146] https://www.gopetition.com/signature/locate/7185726?utm_medium=rss My daughter and I both suffer CFS and this treatment is used overseas to treat patients. CFS has been linked with XMRV and the tests and treatments that provide sufferers with improved health should be available to patients in Australia. This could change our lives which are difficult (beyond expression in this forum) and there is no treatment that works - help us as we don't have the financial means to travel overseas to obtain this treatment. Please!

]]> Sat, 20 Mar 2010 08:36:43 UTC 7185726 Mr. Manjunath N [Signature #145] https://www.gopetition.com/signature/locate/7175311?utm_medium=rss Government are for the people, to the people and by the people.

So lets ask government for medicals costs. Is'nt is a basic duty.

]]> Thu, 18 Mar 2010 10:33:25 UTC 7175311 mr john vinton [Signature #144] https://www.gopetition.com/signature/locate/7162236?utm_medium=rss after suffering pain for fifty years this could be the very thing that may change my life and on all accounts i should at least, be able to try naltrexone,and for the other reason,it is safe.and has verry little side effects.

]]> Tue, 16 Mar 2010 05:12:55 UTC 7162236 ms yee ling wong [Signature #143] https://www.gopetition.com/signature/locate/7142358?utm_medium=rss Sat, 13 Mar 2010 05:06:41 UTC 7142358 Mrs. Karen Pace [Signature #142] https://www.gopetition.com/signature/locate/7139346?utm_medium=rss I have MS..Nothing has worked for the fatigue, the progression, or the memory....LDN is much more affordable than Copaxone.

]]> Sat, 13 Mar 2010 08:08:41 UTC 7139346 Mrs Patricia Reid [Signature #141] https://www.gopetition.com/signature/locate/7107207?utm_medium=rss I have ankylosing spondylitis and so far have had reactions or further medical problems caused by commen medication for this disease.
LDN does not have the side effects I have encountered with traditional medications.
And marked improvements have been noted all arround the world by AS suffers using LDN.

]]> Mon, 8 Mar 2010 09:52:03 UTC 7107207 Mr John Harrahy [Signature #140] https://www.gopetition.com/signature/locate/7107096?utm_medium=rss Mon, 8 Mar 2010 09:25:52 UTC 7107096 Miss Rachael Spinks [Signature #139] https://www.gopetition.com/signature/locate/7087575?utm_medium=rss Sat, 6 Mar 2010 12:16:26 UTC 7087575 Mr Simon Seawright [Signature #138] https://www.gopetition.com/signature/locate/7086249?utm_medium=rss MS Sufferer with no current MS Medication other than pain relievers which hardly work and vitamins, diet

]]> Fri, 5 Mar 2010 06:19:36 UTC 7086249 Mrs Bridget Rae [Signature #137] https://www.gopetition.com/signature/locate/7006070?utm_medium=rss Hoping this truly would be of benefit to people!!
it would be awesome to have trials in Australia.
There is a Doctor withfriends and relatives in WA who have funded hdn for addicts, manufacturing their own. They also now need funding locally.

]]> Thu, 18 Feb 2010 02:23:11 UTC 7006070 Mrs E Parish [Signature #136] https://www.gopetition.com/signature/locate/6933786?utm_medium=rss Wed, 3 Feb 2010 04:14:33 UTC 6933786 Mr Michael Hall [Signature #135] https://www.gopetition.com/signature/locate/6926768?utm_medium=rss Mon, 1 Feb 2010 08:24:26 UTC 6926768 Mr Scott Spackman [Signature #134] https://www.gopetition.com/signature/locate/6873207?utm_medium=rss Fri, 22 Jan 2010 01:27:16 UTC 6873207 Ms Holly Moore [Signature #133] https://www.gopetition.com/signature/locate/6873205?utm_medium=rss Fri, 22 Jan 2010 01:26:23 UTC 6873205 mrs caroline moore [Signature #132] https://www.gopetition.com/signature/locate/6873160?utm_medium=rss Fri, 22 Jan 2010 01:05:44 UTC 6873160 ms aviva vayspap [Signature #131] https://www.gopetition.com/signature/locate/6865451?utm_medium=rss Wed, 20 Jan 2010 08:26:00 UTC 6865451 Miss Lisa Freeman [Signature #130] https://www.gopetition.com/signature/locate/6837585?utm_medium=rss Fri, 15 Jan 2010 05:45:16 UTC 6837585 Mrs Carol Lanzoni [Signature #129] https://www.gopetition.com/signature/locate/6835055?utm_medium=rss Fri, 15 Jan 2010 08:45:41 UTC 6835055 Mr Annit B [Signature #128] https://www.gopetition.com/signature/locate/6820776?utm_medium=rss Wed, 13 Jan 2010 12:15:29 UTC 6820776 mrs caroline moore [Signature #127] https://www.gopetition.com/signature/locate/6801450?utm_medium=rss my interest is in R.A as my daughter and I both suffer from it

]]> Sat, 9 Jan 2010 07:16:26 UTC 6801450 Ms Katherine Watson [Signature #126] https://www.gopetition.com/signature/locate/6784807?utm_medium=rss I have only just become aware of this amazing drug. My son has Crohn's and would benefit enormously from taking this drug.

]]> Wed, 6 Jan 2010 09:51:33 UTC 6784807 Mr Robert McLeod [Signature #125] https://www.gopetition.com/signature/locate/6771480?utm_medium=rss Mon, 4 Jan 2010 04:07:04 UTC 6771480 mrs caroline moore [Signature #124] https://www.gopetition.com/signature/locate/6760660?utm_medium=rss Thu, 31 Dec 2009 09:28:36 UTC 6760660 Ms Claudia Homer [Signature #123] https://www.gopetition.com/signature/locate/6723102?utm_medium=rss It's the compassionate thing to do!

]]> Sat, 19 Dec 2009 11:31:54 UTC 6723102 Mrs Anonymous [Signature #122] https://www.gopetition.com/signature/locate/6713446?utm_medium=rss I have fibromyalgia and would love to have my life back. Just to walk down the beach to the water would be the most amazing thing for me to do.

]]> Thu, 17 Dec 2009 08:23:52 UTC 6713446 Mr Paul Shields [Signature #121] https://www.gopetition.com/signature/locate/6702048?utm_medium=rss Wed, 16 Dec 2009 12:55:39 UTC 6702048 mrs Dianne Osiurak [Signature #120] https://www.gopetition.com/signature/locate/6701034?utm_medium=rss This drug would save the government a lot of money, and as a bonus save a lot of people a lot of angst and suffering.
We need this drug!

]]> Tue, 15 Dec 2009 07:21:55 UTC 6701034 ms bernice dey [Signature #119] https://www.gopetition.com/signature/locate/6681955?utm_medium=rss Sat, 12 Dec 2009 08:50:21 UTC 6681955 Mrs. Jennifer Murray [Signature #118] https://www.gopetition.com/signature/locate/6637953?utm_medium=rss I suffer from ulcerative colitis and have read about the potential benefits of LDN with this condition. I petition the government to make funds available to research this drug to help improve the quality of life for people like myself and with other auto-immune disorders. I have not yet tried LDN but would like to be able to do so.

]]> Mon, 7 Dec 2009 01:10:49 UTC 6637953 Mrs suzanne Ullman [Signature #117] https://www.gopetition.com/signature/locate/6636454?utm_medium=rss Health care does not have to be complicated.

]]> Sun, 6 Dec 2009 08:03:15 UTC 6636454 Mr Kenneth Alan Starrs [Signature #116] https://www.gopetition.com/signature/locate/6632231?utm_medium=rss I'm a pensioner now with a list of autoimmune related problems(connected to my ME/CFS/lifetime illness(?))From what i have read/viewed LDN which is relatively cheap would lessen suffering/make hundreds happier/benefit economies and help many families.It is a must!

]]> Sun, 6 Dec 2009 08:44:48 UTC 6632231 Ms Nonnette Day [Signature #115] https://www.gopetition.com/signature/locate/6615479?utm_medium=rss I was diagnosed with Chron's disease at age 25. I'm now 46. That's a long enough time spent sitting on the loo, don't you think?

Test and release this drug so that I, and others like me, might keep our body's intact, away from the surgeons knife.

]]> Thu, 3 Dec 2009 11:40:28 UTC 6615479 Mr Anonymous [Signature #114] https://www.gopetition.com/signature/locate/6583509?utm_medium=rss Sun, 29 Nov 2009 03:27:42 UTC 6583509 ms marion brown [Signature #113] https://www.gopetition.com/signature/locate/6549730?utm_medium=rss Sun, 22 Nov 2009 12:00:36 UTC 6549730 Mr Duncan Kelman [Signature #112] https://www.gopetition.com/signature/locate/6495427?utm_medium=rss Mon, 16 Nov 2009 07:22:06 UTC 6495427 Mr Stephen Beeby [Signature #111] https://www.gopetition.com/signature/locate/6412591?utm_medium=rss I have been taking LDN for 8 months for a thyroid disease (Hashimoto) I have not felt so well in 6 years!

]]> Mon, 2 Nov 2009 05:11:10 UTC 6412591 Ms Angela Harper [Signature #110] https://www.gopetition.com/signature/locate/6379238?utm_medium=rss Sun, 25 Oct 2009 05:03:21 UTC 6379238 mr kevin williams [Signature #109] https://www.gopetition.com/signature/locate/6366535?utm_medium=rss I have MS and I am interested in any potential treatment.

]]> Thu, 22 Oct 2009 07:08:31 UTC 6366535 Mr Wayne Gilholmw [Signature #108] https://www.gopetition.com/signature/locate/6297753?utm_medium=rss I have AS and want to see if it can make any changes so I would love to see it more readily available.

]]> Wed, 7 Oct 2009 09:08:07 UTC 6297753 Mr Malcolm McLean [Signature #107] https://www.gopetition.com/signature/locate/6276543?utm_medium=rss Unhappy with conventional treatment for RA would like to try Ldn but unable to access in Australia

]]> Fri, 2 Oct 2009 07:50:38 UTC 6276543 Mr MILTON REID [Signature #106] https://www.gopetition.com/signature/locate/6241004?utm_medium=rss Thu, 24 Sep 2009 01:44:41 UTC 6241004 Mr Julio Caceres [Signature #105] https://www.gopetition.com/signature/locate/6186645?utm_medium=rss I would like to support the petition. As patient I need to get LDN.

Thank you.

]]> Sat, 12 Sep 2009 03:30:22 UTC 6186645 Mr Samuel Chalmers [Signature #104] https://www.gopetition.com/signature/locate/6163059?utm_medium=rss Mon, 7 Sep 2009 02:33:46 UTC 6163059 Mr Juan b [Signature #103] https://www.gopetition.com/signature/locate/6154009?utm_medium=rss Fri, 4 Sep 2009 02:55:30 UTC 6154009 Mr Simon Bridge [Signature #102] https://www.gopetition.com/signature/locate/6145171?utm_medium=rss Wed, 2 Sep 2009 11:43:19 UTC 6145171 Mr Gaston Gingues [Signature #101] https://www.gopetition.com/signature/locate/6134027?utm_medium=rss Please, please and please!

]]> Mon, 31 Aug 2009 12:17:28 UTC 6134027 mr frank toth [Signature #100] https://www.gopetition.com/signature/locate/6130248?utm_medium=rss Sun, 30 Aug 2009 12:28:27 UTC 6130248