LDN Petition to the European Parliament

Why are we denied a trial of a safe drug when doctor are quite happy to "drown" you with pain medication wich has horrendous long-term side effects.

This is a theraputic hope for people fighting immune conditions, which is leaving people open to viral infections, which in many cases leads to cancers & further infections & deaths. Medicine needs to be humane. Please hear the voices of those lucky enough to have heard of this. Too many people have died & suffer. Trials now in the UK please please please.

This is a theraputic hope for people fighting immune conditions, which is leaving people open to viral infections, which in many cases leads to cancers & further infections & deaths. Medicine needs to be humane. Please hear the voices of those lucky enough to have heard of this. Too many people have died & suffer. Trials now in the UK please please please.

I have chronic arthritis, cervical and lumbar spondylosis and fibromyalgia and despite attending a pain clinic for years and being prescribed endless amounts of drugs, nothing helps. Imwould love to be given the opportunity to trial this drug LDN. Please help , thank you.

Please fund trails for the use of LDN on auto immune diseases.

This could be a life line for those in chronic pain. Drug companies should be willing to help people who may be needlessly suffering

Have been taking LDN for 5 years for MS, would not be without it.

Diagnosed with Hashimoto's Thyroid Disease over 30 years ago and since then have no idea what a "normal life" is. Always in constant pain or have some sort of illness. To be able to have this medication would be throwing me a life line.

I have Crohn's and have tried everything the doctors can throw at me, currently living life with only half a bowel and bag, I want my life back

Please help fund a trial on LDN !

There are so many people suffering out there needlessly. Please please do the right thing and get LDN licenced.

many people need this drug to function. It is the cheapest, most effective treatment available. Keep it available.

I support the the petition

Please release this drug for use now.

LDN is much cheaper than the conventional drugs that are used for MS, it works better for many of us and also helps many diseases. Why is it not already licensed? It doesn't make sense.

it needs to be approved AND SOON!!

LDN is efficacious wrt SPMS . 5 Years a user.

I've been telling people about Len for the last 30 years it's about time we could have it

ldn has such a positive impact on msers, please help!

I am in full support of this cause.

I am in full support of this cause.

támogatom a petíciót!!

Támogatom a petíciót !!!

I am in full support of this cause.

Hungary

Hope that will do

this works please make it available

Felméry Klára, Hungary, Budapest

SM BETEG.

I am an LDN User I have been taking for over three years now, it is amazing drug and should be in first line treatment before any expensive DMDs (Disease Modifying Drugs). we have over 11,000 LDN Users on one site and hundreds of thousands of LDN Users for Autoimmune Conditions all around the World. All got to to learn about Low Dose Naltrexone through Word of Mouth. Please, Please help us to get LDN recognized so it can relieve the Symptoms of these Chronic Conditions. LDN is not a cure, but it works by rebalancing your immune system and triggering off three times the amount of endorphin your body produces whilst you are asleep, so you have a feel good factor too. I only wish i had known about it when i was first diagnosed with Mutiple Sclerosis and i would not have got as disabled. It can not fix the damage already done, but can prevent the disease from progressing. It is cheap, Widely available, Non toxic, No fatalities, and works to help you live in your body with horrible painful symptoms. Kind Regards Caths Evans.

I am an LDN User I have been taking for over three years now, it is amazing drug and should be in first line treatment before any expensive DMDs (Disease Modifying Drugs). we have over 11,000 LDN Users on one site and hundreds of thousands of LDN Users for Autoimmune Conditions all around the World. All got to to learn about Low Dose Naltrexone through Word of Mouth. Please, Please help us to get LDN recognized so it can relieve the Symptoms of these Chronic Conditions. LDN is not a cure, but it works by rebalancing your immune system and triggering off three times the amount of endorphin your body produces whilst you are asleep, so you have a feel good factor too. I only wish i had known about it when i was first diagnosed with Mutiple Sclerosis and i would not have got as disabled. It can not fix the damage already done, but can prevent the disease from progressing. It is cheap, Widely available, Non toxic, No fatalities, and works to help you live in your body with horrible painful symptoms. Kind Regards Caths Evans.

As a user of LDN I feel that more people should be given the opportunity to use this amazing drug.

This has given me a better quality of life from my demylination syndrome desease

I'm on LDN and been taking it for seven years now and helps me with my mood - bladder - spasms problems and take a 3mg dose

We need this all over the planet. Hoping for a U.S. Campaign as well.

Just do it, as we say for things that are important. Thank you!

I take 3mg for bipolarI and fibromylagia. It has helped immensely, the only medication that has ever relieved suicidal ideation. I accidentally signed this twice using my phone to submit it, so I deleted the duplicate signature. Lisa

I am signing on behalf my my dear friend whose MS has exacerbated in past few years leaving him paralyzed on right side and wheelchair bound. Out of pocket he pays for caregivers to help with ADLs.

This needs to be more widely available

As a regular user I can vouch for its effectiveness. This would be a cheap option that may help many 1000's of people. In these cash strapped days it is insane that the health services cannot make full use of it.

CROHNS,THYROID SUFFERER! IT MAKES ECONOMICAL sense

Once again money and greed overlooks the need of the people's well being

i take LDN it does help !!

I am extremely interested in seeing how this drug can help people with ME and Chronic Fatigue

Europe ,lead the way on this, we in the USA will need to wait longer ,that's for sure. We won't fund anything that doesn't make a big drug company rich.

68 year old man who has taken LDN 4.5mg for one year. Chronic fatigue, chronic depression, and brain fog gone after two weeks. Lymphoma progression halted after 4 months and remains in remission after one year. Constant ringing in ears gone after 6 months but returns occasionally in much milder form. Physically much stronger and happier now with plenty of energy. I have not been sick for a single day since starting LDN.

Make this available!

I use LDN for Mixed Connective Tissue Disease and it has improved my life.

Go ldn

Lets get this recognise not palmed off that the pain is in your head

Please make funds available!

Please get clinical trials for this drug, I suffer from fibromyalgia and do not want to suffer anymore

Do the right thing Europe.

Ich habe Rheumatoid Arthritis und möchte sehr gern mit LDN behandelt werde. Habe aber schwirigkeit einen Artz zu finde der mir es verschreibt.

Please we need this drug.I shouldn't have to get it privately.because my body doesn't work the same due to immune diseases other medecines either dont work or work for a while then stop. or cause more damage to my body.withoutm this drug i would be totally disabled and on other very expensive drugs.LDN is cheap to produce and very little side effects please help us. very sincerely Mrs Y. Thompson

Read so much about this. I'm trying to get a Dr in my area (Glasgow )to prescribe it for me as I have been weaned off the opiates that I've been on for many years for pain. Unfortunately my GP Dr Tom Gilhoolie is not available til Aug and I'm due to take my last tab in 2 weeks and be left with no pain relief. Looking for a Dr to prescribe LDN for me. Can anyone help please?

Make funds available for a trial into this drug. If it is made available it could help thousands

PLEASE give people the chance to access this medicine - it's bad enough being ill without being made to feel like an outcast for wanting a drug that, it would appear, is 2 -3 times More effective than the approved (very expensive) medications..

I love in west Midlands and have had get a private prescription via Scotland. Not easy meeting this cost when tax credit being cut Also working tax credits I need ldn to keep me working

i have fibro

Ldn helps a lot of people - let's give more the chance to feel better

give LDN a chance

I've researched LDN online and in books for over a year, and am convinced it is bit safe and uniquely efficient for many difficult autoimmune diseases - not to mention dirt cheap. It could save EU governments billions in healthcare costs.

Please trial DON immediately!!

My daughter has rheumatoid arthritis and still suffers despite being on highest dose of methotrexate

I've read a great deal about this, then researched as to how to obtain it, and find this difficult to navigate..... as I have too much 'brain fog' a long with Sjogrens Syndrome and Fibromyalgia...... and right now am feeling so very unwell, as nothing offered to me other than 'happy pills' these have serious side effects which I have experienced ....... and am not going there again.

I was a healthy nurse who enjoyed many sports, now I'm almost bed ridden due to fibromyalgia following food poisoning!

Please bring to the UK NHS!

iv suffered for 10yrs and this could give my life back

I have FMs. This trial seriously needs to go ahead. The effects this illness and others has on people's lives is awful. Please allow this trial.

primary progress m.s

Please please please get this licenced We need this

I have secondary progressive ms Please let us have LDN if you lived my body for 24hrs you would understand the urgency of this drug without any hesitation just to allow some peace willing to try aanythinng to eliminate any symtoms

please let us have LDN l have MS and want to try to get my life back

As a sufferer of Fibromyalgia I would like the opportunity to try this medicaton to see if it will ease my symptoms and give me back some semblance of a normal life.

LDN is an amazing medicine,wouldn't be able to function properly on a daily basis without it,it has enabled me to get myself a part time job which without it I definately would NOT be able to do.

This gives a better chance to hundreds of sufferers

Ldn is helping me cure my psoriasis. Please fund a clinical trial

As someone who has chronic pain caused by ME and fibromyalgia,I plead with ypu to researcn this drug, thay many are already finding useful

I am paying for a private prescription of LDN for my Hashimotos. It has drastically reduced my joint pain and inflammation. My GP won't acknowledge any form of treatment for my disease - his treatment plan is for me to wait until I am hypothyroid and then we'll re-assess. LDN helps me manage day-to-day tasks.

Wish we could get it from our GP's !!

please make this a prescription drugavailable on the NHS as i need help! Fibromyalgia can b treated with this and i badly need it!!

Fibromyalgia suffer

I have suffered with fibromyalgia and now know there's something out there that could help me, I've tried everything been off work with chronic pain so I'd welcome this inexpensive drug with open arms. Please run trials it could save the British economy billions.

I have Fibromyalgia we need a cure and this could be a step forward

It is a disgrace to health care that trials are funded by the very people who profit from the drugs being investigated. LDN had transformed my life, yet is a battle to obtain. This is just plain WRONG.

I wish to sign this petition to make LDN available to all. Stage 4 cancer myself and I buy it from Scotland. I support this campaign for trials not for profits for drug companies

LDN would enable me to further control the debilitating symptoms suffered by hypo thyroidism.

Let's give a chance to health, approving the use of LDN

Please some one help us to find ease for Fibromyaglia and other diseases like Rheumatoid Arthritis,MS, Crohns

Alas an MS -r this. Might find re

I sign this petition because my 17 year old daughter has a chronic disease . Any drug that has no known side effects & that could help has GOT to deserve more Government finance for research.

This drug appears to work. There should be publicly funded research.

my self and my daughter have ctd/ucdt.

Its interesting that if you have money you can get this privately from a GP, but a NHS GP wont prescribe it. This could be a breakthrough in treating M.E. ;something there is no other drug for. Desparatly needed. Two friends dead from M.E.

Please do this trial it could help thousands of people!

There is no humane reason to block this from regular prescription use. It is however inhumane and a breech of human rights to leave so many in constant pain unnecessarily .

I'm a sufferer and need this drug made available

Struggling to do my job and have a life with this fibromyalgia. We need help.now.

Should be made available a s a p

For all of those who suffer in silence with this suffering invisible condition

I want LDN licenced for Fibromyalgia so that I can again become a productive member of society.

If it can help people have a next to normal life without constant pain, it needs to be looked into.

I have erythromelalgia, fibromyalgia and arthritis along with other conditions. I need some relief from the pain

I have fibromyalgia

We need this

We really want this to happen sooner rather than later we have been ignored for long enough

I live in Pembrokeshire i have had Fibromyalgia since 2004 i would love to have this treatment anything to get some pain relieve would be great

Fibro is very real and it should be recognised by the heads of all countries, people can't work because of it and other people just call us lazy,

I am a fibromyalgia sufferer but I've been told I can't have ldn but it isn't licensed for my condition.

I'm really fed up being treated like I want 'strong drugs' I want something to help with the REAL PAIN I feel

Help us please!

Just help make sufferers lives more easy please

A drug that can help alleviate the severe pain i go through daily without falling asleep at my work desk would be something.To actually have this recognised as an illness without people thinking youre making it up would be a revelation for is Fibro sufferers.Please help fund this prescription

My mum suffers from fibro and shes getting worse everyday! Please we need this!!

I have MS and would like to LDN for MS, My Neurologist has denied my request for it.

It has already been proven that this is the most effective treatment for fibromyalgia. It should be available on prescription.

As a fibromyalgia and arthritis sufferer, in constant pain and stressed by having no relief from this awful disease. Any new drug or treatment that so far looks promising can only be a good thing.Any feasible treatment to help our symptoms and perhaps let us lead an almost normal life again, is worth its weight in gold and should be available .to us. We need to access this, if it helps any of us that is something better than zero. Please consider this

Please do the right thing and sign!!

i want use this for my fibromyalgia please can you approve it so I can get it from my GP

I have fibromyalgia and feel I should be given at least the opportunity of seeing if this medication works for me through the NHS. I researched and found this information myself but when I approached my gp I was told I couldn't have it. Why? It seems to have benefited many different people?.

Think of the people and not the pharmaceutical company profits. This product is from God why are you stopping me from using it!

I LIVE WITH CONSTANT PAIN AND WOULD LIKE YOU TO TRAIL THIS DRUG LOW DOSE NALTREXONE SO THOSE OF US WHO TRY TO SURVIVE SLEEPLESS NIGHTS PUTTING ON HAPPY FACES TO DISGUISE THE PAIN WHICH IS NOT A BLOODY JOKE.

License this life changing therapy. Save nhs millions over time

disgusting

This needs to happen

This drug could be life changing for so many. It needs to be freely available, on prescription, for those who would benefit from it's use.

I, shall be contacting our MP concerning LDN. I hope everyone will do the same. Thankyou

I am using LDN successfully for M.E, but have to buy it privately from abroad (I'm UK) - It is cheap and easy to do this, but it means I have no medical support, recording or involvement - thousands of us are doing this.

I have MS and this drug could be life changing for me and so many others. It needs to be freely available, on prescription, for those who would benefit from it's use.

hope this helps to get the much needed trial

Get this drug easily available to people who need it NOW. Its cheap, so why the heck not?

Please listen, carefully consider and then act in our own best interests. I thank you.

Please make this vital drug available on the NHS. It could make many lives bearable again. Parkinsin's sufferer.

Please, it will help so many people.

This drug could save huge amounts of money and benefit the many thousands suffering from autoimmune illness. There is no excuse for not funding a trial.

otally agree

This drug can be helpful to so many chronically ill patients who often struggle to get relief from pain using conventional methods, I think the drug should be made more widely available, its not fun living in pain all the time!

Fibromyalgia is robbing me of my life and robbing my husband and children of their mother and wife. Please please trial this drug and let us use it..

The drug should be freely available to all that need it !!!

this will save lives and help people with auto immune diseases get back to work at a low price, saving the NHS vast sums. Lets get it on prescription asap

If the legislators suffered just one day of my daughters' Fibromyalgia, they would do everything possible to make LDN available to the NHS

LDN helped me with pain in my joints, I do not walk now like a robot.

I have struggled with fibromyalgia/ myofacial chronic pain for 17 years with no improvement from drugs, alternative therapies and pain clinics !!! Change is needed!!!

I have a rare skin condition through a faulty gene, this is called hailey hailey disease The skin splits and it is difficult to heal and becomes infected. My GP and dermatologist constantly put me on antibiotics which made me feel ill but through a support group for Hailey Hailey Disease I found LDN. I opted for LDN cream on a private prescription as I am an epileptic and just did not want to take further drugs. My epilepsy has always been well controlled. My hailey hailey disease is now less debilitating and very manageable. My skin has cleared and is nearly back to normal and has been for 3 months now. Long live LDN. I am always telling my friends about it. I hope one day this drug will be available on the NHS. Well done for the work you do.

Ldn worked fo me. We should be able to get it if there is a chance it might work for others. Good luck.

I am using LDN successfully to help control a hereditary skin disease. I have to get a private prescription. It is so cheap why can't it be prescribed on the NHS? Trials would be a great starting point.

I am an advocate of this drug - this seems like the answer Finally to control these debilitating M.S symtoms and from the many frightening and frustrating disease results - I beleive this may finally be the Answer I have been searching - I am Shocked and cant believe that this all round wonder answer hasnt already been given the go ahead?! Please Let LDN Be Aproved Thank you

This drug is so versatile. It should be more readily available.

My wife needs this so badly

I have HHD and LDN helps our conditions which is hereditary,which includes my sister & my daughter

I have a rare skin condition via a faulty gene it is called hailey hailey disease when the skin splits it becomes difficult to heal and becomes infected I have since joined a support group for fellow sufferers of HHD and have since found out that sufferers in other countries are able to get LDN with amazing results so please let LDN be approved and be available on the NHS

My mum is about to try this drug for hailie hailie skin disease and is meant to of helped thousands!!!!!

This drug could do so much good!

this is important for improving the health of many people affected! :)

It is a miracle drug

LDN should be available for everyone immediately.

I have been told that this drug can help with my rare skin condition - please give us suffers a chance

I would try LDN to control the effects of Charcot Marie tooth disease.

There is no logical reason why LDN should not be made available via NHS prescription. I simply cannot understand - It has a long safety record at much higher doses, it is cheap & seems to have benefitted so many people. What is the problem? I guess it is all about big pharma profits again & lobbying against a cheap, effective out of patent drug - so no profit to be made! Do the right thing UK & EU Get this sorted without delay please.

I would like the drug to be made available to ease the symptoms of Charcot Marie tooth disease.

Suffering from fibromyalgia first diagnosed in 1992. . this condition has now completely made my life unbearable and nothing that has been prescribed to me by gp has worked.

Common sense must prevail as this drug in higher doses has been in use for so long. The trial could surely only improve life for so many.

This has proved crucial for a number of others who have suffered from my father in law's condition.

Poland

I have Fibromyalgia and its so frustrating when there's so few drugs for treatment of this condition. Over the last 6 years I've been signed off from work (I work in the NHS) for several months at a time due to major flares of Fibromyalgia. We need more treatments

If it relieves just a few of my symptoms the quality of my life would defineatly improve along with many others.

Please make this available.

LDN is currently increasing life quality and saving the lives of many. There are many years worth of clinical evidence showing efficacy, way beyond that of placebo. The UK government have said in essence, that a drug company needs to pay for the required trials. Knowing full well that there is no profit in it for them, hence no incentive. LDN can save massive amounts of money in health care. I really see no plausible excuse for not funding the trials and making this properly available to those that need it. It has been clinically shown to be safer than most drugs already offered to many people. Naltrexone has been proven clinically safe and FDA approved at 50-300mg. Again at 8mg and combined with another drug and called Contrave. To then suggest that doses of 0.5mg-4.5mg may suddenly become unsafe is ludicrous.

I have had great benefits from LDN, couldn't manage without it.

Such a great drug! Please do more research!

I personally experience the benefits of LDN every day!

I have under active thyroid and fibromyalgia

it works for most and at worst it does no harm

Doing this for my best matie Sammy.

It really is a huge human scandal that Doctors are unable to prescribe this cheap, safe drug for cancer, fibromyalgia, and other auto-immune diseases. So much unnecessary pain for so many, so long. And we call ourselves a civilised society!

I have Crohns and RA and am on a plethora of drugs with nasty side effects, LDN offers a potential alternative.

I suffer from Myasthenia Gravis and Lupus - I am just having another flare up. What does this mean to me? The ony drug that I am allowed is a steroid called prednisolone - it eventually works but has horrendous side effects which impare my quality of life in a severe way. I have just found out about LDN and cannot believe that I cannot be prescribed this drug when it is readil available in the USA - it is also very cheapo in comparison to other drugs that are used. It has been used on many auto immune illnesses and has been successful - why am I being denied a human right that will do me no harm

im being fobbed off trying to get this , 1 gp , 1 specialist so far when my friend-who isnt even a doctor - prescribes it for her clients with drug and alcohol !!

Please help the people that need this drug,my sister is one of them. Thank you.

Very much needed!

I think this is such a positive and enlightening petition, especially as I've been recently diagnosed with MS. With best wishes Alexandra Cawdron

It is absolutely vital that trials for this drug go ahead ASAP.

Please allow for clinical trials of Naltrexone. Long term it will cut costs on NHS but it is having a positive impact on people with auto immune conditions where other drugs have failed.

We need this medicine to be more accessible.

Please make these trials available asap.

This kind of drug should not be refused to the people who really hold up this failing country. The drug companies are showing their evil side too often.

It's been a struggle to get LDN,this isnt fair,we shouldn't have to beg for this medication which could giive me some life back

My current drugs are very expensive and have terrible side-effects I need to try LDN

I am in pain all the time, if I could take this and it worked it would replace four expensive drugs I'm on. And it's cheaper as well.

i would take this drug now if i could get hold of it, it seems much safer than the methotrexate they want me to go on

It is clear that there is much anecdotal evidence but not much in the way of rigorous, large scale testing. If we have cheap , readily available drugs that have potential to treat other conditions then clinical trials should be enabled ASAP.

This is very important research. The results could help improve the lives of billions of people!

LDN is helping me with Hashimoto's. I am feeling better physically and emotionally.

People need to have the option of LDN. It has made all the difference in the world to me for pain caused by Rheumatoid Arthritis and Hashimoto's Disease.

because it is silly not to!

Let us have the option - this is a cheap safe drug. Like others have said, it is silly not to let those with autoimmune conditions such as lupus, sjogrens etc try this.

I would like more people to know about this really wonderful drug

Please support trials which will help make this drug more easily svailable to those who can benefit from it. Thank you

This is needed NOW. So many people are suffering unnecessarily for the sake of pharma companies financial gains.

It seems very sensible to invest in trials of this drug when it can save billions in future and provide a better alternative to current harmful medications.

Will this petition be of any use if we leave the EU? Has there been one to the English Parliament?

Please provide the funds to help change the lives of so many. Money is available for those who choose to take drugs and alcohol to help them recover. Those with the illnesses that this drug could help have not chosen to become ill. Please allow funds to help these people (myself included) who need something to help them have quality life. Thank you

I'm so glad through my American friends I have heard about this I have fibromyalgia & PTSD

It makes good financial sense to add this treatment option to the list of what is available, as well as being the compassionate response for people like me, in chronic pain since we were young adults, who want to work and contribute taxes, not live on disability benefits while currently approved high cost, high risk treatments fail to deliver improvements or relief, treatment after treatment, while the years go by.

We must all do what we can to cure this horrible affliction

this is important work , and should be supported

The number of cases of Fibromyalgia and similar conditions, are increasing exponentially with severity from mild to severe. The impact on the economy is substantial and yet the government is not giving it the attention it deserves. Its study and the trialling of drugs for its treatment should be a priority now.

This medication is crucial to helping /improving a persons actual health and wellbeing. Make to available to all who need it NOW

For anyone suffering with one (or more) of the conditions this drug can help, life can be a constant, exhausting, frustrating battle. A safe drug that has the potential to help should be made available for those who wish to see if it helps improve their quality of life. The knock-on effects would mean GPs and hospitals would need to spend less time and fewer resources on supporting depression, chronic fatigue, food intolerances, skin complaints, infections caused by low immune systems and on and on... How can making this drug available NOT be a good idea?

As an ME/CFS sufferer, like countless others who have been robbed of a life, this drug could help improve our symptoms and give us a chance to feel well enough to be involved and enjoy life again. At present there is no treatment for ME - we are just left to suffer to put up with it.

I think LDN should be given the chance to be tested clinically as it had already been tested by doctors and their patients in USA , Canada ...

Drugs like this need to be easily accessible help save lives of unfortunate people.

Please please try and get this drug licensed in the UK so lots of us can get a normal life back and save our NHS millions of pounds to spend on training new doctors and nurses and building new hospitals

I agree

please I beg you save my son before it's too late. I know you can. Please please start the trials NOW

Please help bring relief to those in need, by making LDN readily available to thousands of sufferers. LDN is elieviating and liberating many from unnecessary trauma and promoting better personal health. Thank you

Everything possible should be considered to help people with ongoing chronic and painful conditions.

LDN should be a first line treatment for autoimmune disease, it works for the majority and has few side effects - none of which are damaging like other drugs. People come first not profits and profit is the only reason this relatively harmless drug is not prescribed as a first line treatment.

Thank you Jayne and friends in furthering the future of LDN and broadening the minds of the uninitiated! Best wishes

This drug which is so cost effective for the NHS and helps so many should be on prescription throughout the UK after all it will save the NHS a lot of money and help the suffering of people like us.

LDN has been proved to help people in constant pain due to a variety of auto-immune diseases. It is a cheap drug & could save the NHS a lot of money.

I have RA and LDN was part of the treatment prescribed to me by my integrative medical doctor in Ottawa, ON. I am now 5 years RA drug free and feeling great. No one should be deprived of this drug ever.

As this drug is only available on prescription, it is not available to us to use. Either make is an over the counter drug or make it available to us on prescritionon. It will save lots of money on benefits and on not needing useless expensive drugs and it will mean people will not need so much time off of work.

I am having a lot of trouble obtaining this drug as my gp hasn't even heard of it . Im sure it would help my condition but instead I am in a lot of pain because I can't obtain LDN from anywhere. Jacqui

It's cheap and in the long run will save the government a lot of money that they can better use elsewhere but more importantly will help ease the suffering of thousands of people!

hopefully this can help thousands if not millions of people

Given the experience of many doctors in the field this should be taken forward and made more widely available,

Thyroid patients suffering

I have fibromyalgia. The medication I use is not very affective in helping my symptoms so I want to have the option of using LDN. I want my life back.

Yes, it works!

LDN has changed my life for the better, I really beleive it is a travesty that it isn't widely available, it can transform lives and save huge amounts of money on prescriptions for other medicines and expensive treatments

save money and quackery of big pharma

I would like to try this out and improve my health problems. Pharmaceuticals want to make money - with all their toxic medicines, so that is the cause of the apathy standing in the way of their researching this medicine!

Big Pharma is the problem... no profit in a medicine that works and is cheap!

My Fiancee was on LDN until our doctor was nearly struck off for suggesting its use. It was the only drug that got her out her wheelchair and walking again, now we cant get it and are finding it hard to apppoint a GP that can prescribe this in Scotland UK. She is back in her chair now and dealing with chronic pain, NHS. Nicola Sturgeon, back this one PLEASE !!

Sounds like LDN helps to treat the cause not just the symptoms. Would love access to this for RA.

LDN is helping my crohns disease a lot.

please fund trials and research of LDN especially for Crohns

The NHS have told my husband they can do no more for his advanced prostate cancer - he has nothing to lose by trying this drug, and possibly his life to gain - the result will also advance knowledge about this drug.

This drug needs to be made available for use by those suffering these awful diseases.

Any drug that is safe and can bring relief to intractable conditions should be widely available.

Please let this be done to help so many sufferers.

Help us to help ourselves!

Please help

Low-dose naltrexone offers hope to so many people suffering from a plethora of diseases. May God's power bring about this much needed breakthrough.

I have recently been diagnosed with cancer and find it so frustrating that LDN treatment,let alone in combination with iv ALA is not available anywhere in Europe.

We need to bypass big Pharma and have this drug licensed for diseases which create misery and for many poverty through being disabled and unable to work.

Why is this effective and cheap drug not available throughout the EU?

Let's do this!!

My wife suffers from Fibromyalgia, ME and has neuropathic back pain. My wife struggles on a daily basis just to get by. This drug should be made widely available to help suffers of chronic conditions to lead pain free lives.

Why can't those of us suffering from Fibromyalgia be prescribed this low dose, cheap medication with few side effects? Doctors are willing to prescribe far more expensive drugs with serious side effects.

This could heal me - please give this drug the trial it deserves

For the health of my wife Grace who has breast cancer.

We are all ware that pharmaceutical companies don't want to fund research into drugs they cant sell. What is being done to research (with a view to making available) drugs that fall into this category which appear to be useful and effective but need corroboration from the conservative scientific community??

This drug at low doses seems to have great results in treating so many issues auto immune disease, depression, even some cancers. It could address the issues with the new regulations on chronic pain and opiate prescriptions. I feel hopeful about my future for the first time in a long time

I have fibromyalgia & I suffer really bad with it,We need this Drug to widely be avaliable to every person.please please Do This Now

This drug has helped so many people, providing symptom Relief of many conditions, without side effects and is cheap to produce. Symptom relief should not be a matter of how much money it can make but efficacy.

These is a strong body of evidence that making this cheap drug available to people living with cancer would have important benefical effects - I am living with cancer and have to jump through many ridiculous hoops to get hold of it. Please make the sensible decision to make this drug available to people with cancer

I have a lifelong alcohol addiction, and chronic sarcoidosis, stage 3/4, plus psoriasis, and psoriatic athiritis. So many uto immune diseases. Ive tried everything. Im going to try this, but Ive also read that up to 70% of drugs bought online are fake. Is there a completely safe way to buy this please?

Suffering from fibromyalgia and chronic fatigue since 2007 all melds have failed to help. My GP will not prescribe LDN, feeling frustrated and angry

CHEAP EFFECTIVE TREATMENT FOR A WHOLE RANGE OF DISEASES SUCH AS LDN NEEDS TO BE AVAILABLE NOW TO ALL

I suffer with fibromyalgia we need this drug trialling as there is no one drug that works for all sufferers so the more types available the more chances we get of having something that might work for us.

I am trying to get my GP to prescribe me this.

I have fibromyalgia so support this whole heartedly

IT IS A SCANDAL THAT THIS PROTOCOL HAS NOT BEEN MADE WIDELY AVAILABLE AND THAT NEITHER GPs NOR SPECIALISTS ARE EVEN AWARE OF ITS POTENTIAL TO CHANGE LIVES FOR THE BETTER. WHY WAS I NOT MADE AWARE OF ITS POTENTIAL DESPITE SUFFERING FROM BOTH FMS AND IBD,AND DESPITE THE MEDICS HAVING NOTHING TO OFFER FOR FMS IN PARTICULAR. I HAVE ALREADY LOST 17 YEARS TO THESE CONDITIONS. I INTEND TO CLAIM MY LIFE BACK BY TRYING LDN,SO PLEASE RECOGNISE THE NICE TRIAL AND MANY OTHERS AND MAKE IT EASILY PRESCRIBABLE FOR PEOPLE WITH INFLAMMATORY CONDITIONS!!!

Am 57 years old male living in India and I used LDN for sjogrens syndrome. Within 1 month it gave amazing result for me. I strongly recommend LDN as a drug for autoimmune diseases.

It is time the government took action to help the people regain their health without big money going to Big Pharma. This is cost effective and only benefits the individual. I will be seeking it out.

Seems like a no brainer to me. The drug does no harm and is cheaper than most other medicines - it just makes sense

Sounds very good to me. Let's get it now!

I support this petition.

If we have something that can help people then please use it

My part uses LDN, and it is truly lifechanging, for the better.

This drug should be made available to all

Please please, ldn massively helps my lupus and Sjogrens flare ups that are crippling

Please safe my live and my son live with LDN

WHY HAS NO DOCTOR EVER EVEN MENTIONED THIS TO ME.AFTER 17 YEARS OF FMS I HAVE DEVELOPED BOTH UC (2004) and now RA.ON SEEING RHEUMATOLOGIST RECENTLY I ASKED HIM ABOUT IT AS I WAS LEAVING.HE SAID HE WOULD LOOK IT UP BUT I HAD TO CORRECT HIS SEARCH WHEN HE ENTERED NALTREXONE RATHER THAN LDN. THIS IS A SENIOR CONSULTANT AND PROFESSOR OF RHEUMATOID ILLNESSES,BUT HE HAD CLEARLY NEVER HEARD OF IT. I AM GOING TO SEE MY GP ABOUT ALL THIS TODAY.DETERMINED TO GET AN EFFECTIVE THERAPY HAVING BEEN LAID LOW FOR PAST 8 MONTHS WITH STUBBORN UC FLARE UP. I WANT MY LIFE BACK,HAVING LOST NEARLY 20 YEARS TO THESE CONDITIONS AND LEAVING WORK IN 2,000 AS A RESULT.RECENTLY DISCOVERED THAT COLAZIDE WHICH I TAKE IN MAX DOSES OF 3X3 p.d. COSTS APPROX £60 per month.SO SURELY THIS IS AN ARGUMENT IN ITSELF FOR MAKING LDN ACCESSIBLE ON NHS.IT WILL SAVE MILLIONS OF POUNDS AND THOUSANDS OF SUFFERERS!!!

LDN saved my life. When I was diagnosed with Multiple Sclerosis my life was halted! Before my diagnosis I was a power lifter and an avid runner.. suddenly I couldn't walk more than 20 feet without stopping for a break. I had brain fog, my job as a professional MRI technologist became extremely difficult. Everything became hard for me, including vacuuming, pushing shopping carts and driving. My vision was compromised and my sense of smell was disrupted. Two weeks after i found LDN I was sprinting again and lifting weights! I gained my clarity and strength back! I tried the normal CRAB drugs, including Copaxone.. which made me gain weight, loose my hair and did nothing for my symptoms. I pray that LDN will reach the hands and ears of Doctors that will help us with these debilitating deseases.

As a fibromyalgia sufferer, who has tried many drugs and still doesn't get full relief from pain, I support this move to get LDN trialled. Thank you.

I'm sometimes completely incapacitated by pain, and most of my 56 years have been characterised by "growing pains", "rheumatism", "spinal and joint deterioration" (at age 27!) and, of course, numerous complete-body 'flare-ups'. I would love the chance to try LDN out and possibly be able to play with my young and incredibly energetic grandsons before they reach puberty! Thank you for reading.

LDN works wonders for my son who has B12 deficiency and Pernicious Anemia

My daughter was diagnosed with ME 27 years ago and ceoliac 7 years ago. She has various symptoms but the most debilitating one is dizziness.

I sign this petition

Could be lifesaver

Hurry up - thousands of us are suffering

I have suffered for 30+ years with the after effects and side effects of Graves' disease and now I am being tested for a serious auto immune problem as a result of the remains of my thyroid which was removed. Please help . I am not the only one suffering. LDN will save the NHS money and improve the quality of life for hundreds of thousands of UK citizens.

urgently needed, particularly as the NHS no longer performs clinical or functional medicine would save lives and NHS

Crazy world of suffering! This can help & stop so much unnecessary pain. Please- health life over profit

This is common sense in action. Let's do it now.

please let me know how you get on I have chronic fatigue syndrome and thyroiditis with antibodies...my specialist cannot stop my immune system attacking itself and standby will my thyroid my health and my life disintergrates, I urge you to please make this drug available to all suffers, with ultimately the added benefit of saving the NHS a money for the NHS .

It is a human basic right to have access to medicine that improves ones quality of health

Please give us hope to heal.

This is so importantant for peoples health conditions please LND tested as soon as possible.

I suffer from MS and I desperately need help as my mobility is terrible. I am not able to work and have to try and manage on the lower rate of PIP this is not a nice position to be in when you know there is no cure for MS. I desperately need something to help m

So many people could be given their life back as a result of making LDN readily available.

I have MS and have tried all the drugs of which the terrible side effects are too overwhelming so LDN would be very beneficial to me.

I wholeheartedly support this initiative, one of the most sensible proposals I have come across.

I'm a RLS and polymyalgia sufferer. Please allow me to have this drug

I have been ill with multiple auto immune diseases for over 20 years, please give me the opportunity to enjoy what is left of my life.

Please give us a chance at improving our lives with this drug!

Both my sister and I could benefit from this, please make it available.

This is quite obviously an absurd situation and needs addressing immediately.

Please end our suffering and make LDN available to us. Millions must be spent on drugs that don't help. It will be much cheaper to make LDN available to those who need it.

Please hurry up, and help people and institutions use the potential benefits of this drug.

Just because it is CHEAP should not mean that pharmaceutical companies ignore this harmless and effective treatment for autoimmune diseases.

.....because we need new viable and affordable options. This is about people suffering unnecessarily.

We would spare patients chronic symptoms somewhat more effective than drugs used now and save lots of money within the NHS

My daughter suffers from hashimoto disease and I would like this med to be available on prescription.

This drug needs to be made available on the NHS. I suffer with CFS and fibromyalgia and would love the opportunity to gain the relief this drug could give me

Signing for all uat sufferers!!

Personal interest regarding ldn as a treatment for Hailey Hailey disease....Glad to be part of the petition.

I have a painful variant of Primary Restless Leg Syndrome inherited from my father. I also have Polymyalgia. I wish this was prescribed by the NHS instead of having to get a private prescription.

It is a CRIME that we are deprived of our human rights medications. But is it the fault of the Government, Big Pharma or Doctors. The Gov.do not care as it is not there money. They still have there returns in their Investiments, and also Private Insurance. BIG Pharma very GRIDDY. What do we say about Doctors are they as Ignorant as they make out to be or there some hidden agenda as to why they will not prescribe LDN. Are Is it really down to money. I been a sufferer for 30 years with ME Fibromyalgia Low Immune System. I have not left my house for 6 years or played darts or any other hobbies. (Lets hope that in the mean time they do not Change any thing on LDN)

Make this drug freely available now to help relieve suffering.

We were lucky to get LDN from the source: https://www.buyldn.com/ (without prescription). It helps my mother with pancreatic cancer. We really hope it will work so good in the future.

Please make available on NHS

I very much want to see this drug have clinical trials so that people like my oncologist will have more faith that it will only do good. Currently it has had no randomised trials and so will not look into it. Please do something about it!

please I urge you to take on board the mountain of evidence which is proof that this is working for many people that are highly sensitive to high dose drugs. Its approach if far reaching. I am a patient & what alarms me, is just how little the NHS is being taught about it, furthermore the stonewalling of the present Government. Lives matter over profit & The NHS needs new ways to support its budget. Patients need to be listened to & Consultants need to be acknowledged for their persistent research & support with LDN.

Please make doctors aware of this drug

Please make LDN widely and cheaply available in Europe, it could help so many people and crippled health systems

I have had fibromyalgia for 15 years plus, and the daily pain is to the point I have thought of ending my life! Just to go 1 day pain free would be amazing! And to sleep for a whole night would be out of this would. I am on the strongest drugs I can have but it doesn't even touch the pain! So please consider giving Ldn a trial and make millions of people pain free , I for one plead for a you to give us a break! Regards yvonne Walker

I have been using this for years, I have MS and I think I'm saving the NHS loads of money. I have to pay for this drug and have to get a private prescription, it would be so much easier if it was used by the NHS.

I have severe Alopecia and feel LDN might help my hair to regrow as had none since it started 3 years ago. I hope the drug goes through trials and gets licensed so it is readily available for doctors. Thank you.

Ive heard this drug sends Fibromyalgia into remission. This should be available as the prescription drugs do not work.

Please start the trial asap

I have suffered from fibromyalgia for over 5 years. For 2 of those I have taken ldn with significantly positive results. It took me 12 months of funding this medication through a private physician before my GP agreed to take a chance and prescribe it for me. This is because its not approved by the FAD. Please make this widely available. The alternative medications all carry hideous side effects which ultimately stopped me using them.

I strongly support this drug trial after doing so much research on LDN and its positive benefits for autoimmune diseases. I myself have suffered from Rheumatoid Arthritis since October last year and am now taking LDN. Although I have only been on LDN for 4 weeks, I feel good and most of my RA symptoms have improved a lot. I hope that the trial of this drug can be done asap and the relevant licenses can be achieved so that more people can be benefited.

Poszukuję skutecznego leku na RZS. Naltrekson jest dla mnie nadzieją na życie bez bólu.

It's a no-brainer really.

I have been on LDN for 10 months and I feel like I have been given a normal life back after years of suffering a number of hard to diagnose or hard to treat diseases. After taking LDN for only several weeks, I had dramatic improvement in a number of conditions I suffer from including ulcerative colitis, fibromyalgia, osteoarthritis of the knee, secondary endolymphatic hydrops (similar to Meniere's), treatment resistant atypical depression (finally achieved full remission after 15 years of only partial remission on drug therapy and psychotherapy), and a strong improvement in hypothyroidism, blood glucose, and stubbornly low vitamin D levels. My energy level has improved dramatically with decreased pain and fatigue, and I feel like I have my life back again. I have suffered no noticeable side effects and am able to tolerate sustained exercise. Ten months now on LDN, I continue to be amazed that I am continuing to feel so well after years of low functioning, that my life had fallen apart in many respects. It seems too good to be true that a safe, inexpensive drug with few to no side effects can make such a remarkable difference. It truly is a humanitarian cause to support for all the potential good this relatively unknown medication can do from addiction, to pain to cancer and autoimmune disorders. Please fund the research program for this potentially history-changing medication now. Thank you.

Having being diagnosed with ME and now having to potentially give up my employment due to the severe symptoms I am experiencing, is it not more cost effective to allow the prescription of this medication as opposed to me claiming benefits which I loathe to do?

I use this and it helps me with my ME

I don't know what this is,I've been hyper graves for 4 years.keep threatening to stop my meds unless have two or op,I think due to Costa rather then care.anything that aids research and is alternative to fire treatments on offer.Thyroid is chronic illness and should receive the same public awareness,advertising for funding for research as the one that monopolise the charity business.The government should fund thyroid Treatment and research and fund necessary medication,not funding this Is leaving thousands suffering or forced Into rai and operations,while some may be ok,it should not be russian roullete with our quality of life.we paid our contributions we are entitled to recieve the proper treatment many are unable to work thyroid is so debilitating we receive no benefits for at hyperthyroidism (graves disease).it is time thyroid was given the same pivotal position and attention as the one major charity to raise awareness and finding for research.I always worked have been unable to die to chronic symptons.I won't be forced to Gibson's choice treatment that at leave me with no quality of life,so this alternative treatment is necessary, essential urgently needed by thousands suffering thyroid disease.we are entitled to treatment not just a death sentence,the present treatment no gaurantees,your on your own in told,not a lot they can do once had the treatment of not worked.For some it will,before we have to have last resort we deserve a fighting chance,many thyroid sufferers will have gone through a rollercoaster of tests and treatments for varying years.we have suffered long enough we all deserve the choice,all we have at the moment is Gibson's choice which I don't relish.colleen wilson

please sign the petition people this is great it works

This drug ca surely 'do no harm' in all areas of autoimmune disorders where answers are very often hard to find.

As a parent watching her former 15 year old suffer with autoimmune disorders of hashimotos disease and pots syndrome dysautnomia and chronic fatigue grow into a 20 year old who has no quality of life, whilst various departments cannot agree on a medication that suits all conditions LND offers just what she needs to give her a fighting chance of living a life where she can engage in basic activities such as washing, cooking and walking with out suffering.

These drugs need to be available to relieve suffering.

Please sign this for a dear friend of mine

Why is this not yet available? Because it doesn't make money for the drug company. This drug could save the NHS millions and eliviate the pain for fibro suffers and many other conditions. Shouldn't people come first not profit?

I have fibromyalgia, and understand many others who suffer have received relief from LDN

Please make LDN available to the public!

Please fund a trial of low dose Naltrexone for use in multiple sclerosis

I sign with confidence to support LDN clinical trials NOW please

Please assist patients in relieving their unecessary pain/discomfort by providing funding for this treatment which is already proving beneficial tomany

I have suffered from RA for years and nothing works for long and worse, I have been seriously harmed by 'safe' drugs. Please give LDN a chance!

Please help fibromyalgia sufferers to have free access to LDN because it will help us have a better quality of life with reduced pain and could us some of us to continue with a job we want to do.

long overdue

The Government/NHS sd take control of this cheap medication to stop the pharmaceuticals giants ripping them off.

This is very important

This drug low does naltrexone has saved my life and it should be proscribed on a medical card for prevention of the old cycle of alcoholism coming back if it’s worked for me it will work for others I used to drink 2 bottles of scotch a night now I’m down to A drink or 2 every 4 weeks !! What will happen if this medication is taken away !!! Prevention is better then cure punishment does not work for all !!! Addiction is punishing enough so help prevent it happening !!

Trials so overdue

I am a sufferer of Fibromyalgia, chronic fatigue syndrome, osteoarthritis,Lympoderma, sleep disorder & I suffer 24/7. The meds I use now don't make me pain free or symptom free & I'm so tired with it all. I think if their is a safe drug out their why oh why are we sufferers not getting it!. Gwen Legge UK [email protected]

I suffer really bad from a condition called RLS(restless leg syndrome) it will not let you sleep.

I want to use this as a safer option than hydroxychloroquine,which I am taking for my autoimmune diseases hashimotos and sjogrens...

Thank you!

There is clearly no financial incentive for drug companies to fund research into LDN and other low-cost drugs, so we can't rely on them to have our best interests at heart - profit is their motivation. Do the right thing and fund this and other similar trials for the good of the many not profit for the few.

All for this...

Please trial ldn, it has the potential to change my life!

I am more than happy to sign this, I have PBC, and anything that will help is a bonus

I want to use this drug for alchole misuse. How an I get a prescription if it is not liscenced. My only options would seem to be using an onlineharmacy pharmacy which is illegal ,dangerous and very expensive.I donot want to suffer yet another relapse. The pain and humiliation are unbearable.

It is keeping me alive. There is mounting evidence from St Georges hospital London.

let people get well not big pharma get richer, about time you looked after the people and stopped looking after greedy pharma ,, we the people are fed up with greedy pharma only interested in big profits its a sham

Ldn virker på fibromyalgi, det har hjulpet min datter ø, til et bedre liv og hvis det var lettere at få udskrevet, var vi mange flere der var smertefrie.

Please, make funds available for research in the use of Low Dose Naltrexone

I want my daughter prescribed this as she has tried levothyroxine and felt no better. She is 18 years old and is like an 80 year old woman

yes please

Please make funds available for more trials and research, Licence and make LDN available to all in need of it.

I have been diagnosed with Graves Disease after 3 Recurrent Miscarriages. I feel LDN would give better outcomes to those in the same situation as myself.

This drug should be made available on the NHS to help so many people who can benefit from it, and they should be able to have that choice !

I formally request that you intervene to alleviate unnecessary suffering! I believe this is called democracy when those elected take note from the electorate.

I've been on many poisonous drugs from specialists that had horrible side effects. None helped, they made me ill. I found LDN and get it privately and I no longer have pain or inflammation in my joints. I've had inflammatory arthritis for 16 years and suffered for 14 of those years before finding LDN. LDN works, it's cheap and it is not toxic. I can not get it from my GP or Rheumatologist. WHY? I no longer have any faith in my GP or Rheumatologist.

I have an underactive thyroid.G,A.D. Iam having great difficulty getting this med.Online Pharmacy are charging almost £200 for these tabs a serious cociquence of them not being available in all pharmacies in E.U

I like many others need to be able to get LDN on the NHS.

This drug needs to be made available on the NHS. I suffer with fibromyalgia and Osteoarthritis and would love the opportunity to gain the relief this drug could give me,please agree to a trial

Im using LDN for crohns and it works ! yes its not a cure but again there is also a cure for crohns the crohns vaccine (map Vaccine) that the government also won fund ... with OUR Money !!!

I really want to try this drug for chronic Fibromyalgia and CFS

We need this

To think health is about money!

I would love to have this available in the USA

LDN needs to be made available. There must be an organisation owned by the government for out of patent drugs to stop NHS drugs being controlled by pharmaceutical companies profit margins

Yes to LDN

Do it for the people.

This generic drug is so obviously beneficial and cheap, so why doesn't the UK Government or the EU provide funding for a clinical trial so that LDN can be brought into common useage

We need to get his drug Licenced asap,then so many people can get the benefit, especially as this is not an expensive drug. It make so much sense and would save the NHS millions of pounds.

It would help so many people and be affordable.

L.D.N. is a life saver for people, animals and the N.H.S. please please research and use it

Our society desperately needs this drug to stop autoimmune sufferers from having to give up work and going on benefits when their serious autoimmune, painful conditions cannot be adequately treated. I am speaking from experience as a sufferer as well as an employee of the NHS.

we need to have this drug available for people who have nothing else to help them e.g. M.E/CFS & FM

This needs to be trialed now to save the NHS money and help many people

User of LDN

I am a 35 year old sufferer of Hashimoto's. Diagnosed at 22 and have gone into remission once but with ongoing flares. Scared about my future health status as there are so many things I want to do to give back to society and achieve other goals. This condition quietly affects MILLIONS - please let us trial a new treatment that may result in saving the NHS or future system a lot of money and create a happier society.

This drug should be available for everyone.

This would turn the lives around of so many patients, families and children afflicted or children impacted by having poorly parents. It would save the country billions in NHS costs, through saved inpatient and outpatient appointments, GP appointmnts, prescriptions, sick benefits and days lost to work and the economy

Please help

Scandalous to put profits above patients- Drs "Do no harm- this drug does NO harm"

Please help to make our lives more bearable. Other medications are not helping anymore.

This must be done I live with fibromyalgia and need an effective treatment. I know LDN won’t cure me but it might help and that is all we can really ask for.

Thus drug makes financial sense and would save money in the long term.

I have had Fibromyalgia for over 35 years, it has stolen my life. The pain, fatigue and cognitive problems are intolerable. Please help us.

MSK, FIBROMYALGIA, BOWEL CONDITIONS , CHRONIC MIGRAINE

I am a 61 year old lady suffering with RA and it’s debilitating symptoms. Please help.

Works brilliantly for depression too.

Taken this drug for years for M.S. as it is the only drug available to me. All I know is that if I stop taking it my symptoms get worse.

This needs to be readily available on the NHS to be able to help those in need, the people suffering with pain. Anything that helps alleviate the pain is surely a good thing and needs to be trialled.

I and other members of my family use LDN for autoimmune conditions with good results.

Please, my 19 year old daughter and myself need help with fibromyalgia. It seems I also have other autoimmune diseases too, This affects our quality of life so very much. Nothing really seems effective in relief. I have read encouraging evidence of help by taking low dose LDN. Please consider making LDN available. Thank You

We need this to become a reality for those of use with this disease.

I would be more than happy to be part of the trials and research for LDN. I have Hashimotos and it has been shown to have life changing effects for some people with my condition

I have been taking LDN 2.5mls daily for a year for Lyme Disease associated pain. It was been the only medication to relieve the agonising pain I have throughout my body and with NO side effects. I now have a better quality of life thanks to my GP ,who listened to my rational for LDN and prescribes off license.

I support the LDN trial because unless there are trials we may be denied treatments to end our suffering.

This medication is a life saver. European Parliament has to consider that!!!!

I have SPMS and LDN is the only thing I take that really does help.

.....I have friends who pay mega bucks to get this privately, cos it really helps them immensely.....if Chris Steele is for it , then so should we all be....

Ndl can help so many, while saving money too. It needs to be made widely available.

I get this privately and wish the NHS know more about it and prescribe it. More needs to be done to make this available to all and more knowledge.

My daughter has this on prescription from Ireland because we can't obtain it in the UK!! Something is wrong!

If T4 is not effective enough and T3 too expensive, why not try other treatments?

I have found ldn very sith my autoimmune.

I am being prescribed high dose Naltrexone for the treatment of opioid addiction. It is doing its job of keeping me off opiates. During my research into Naltrexone I stumbled upon its use in low doses. This is very interesting and I wish every success to this campaign.

If its approved in USA, why can't we allow it in UK. I am suffering from Hypothyroidism and looking into LDN to improve the symtoms

Lidia Orlikowska

Popieram petycję

I have fibromyalgia and uses LDN with a very good result. I believe that this therapy should be thoroughly examined and widely available for other patients, for many suffering people.

We need to get LDN available ASAP

I want to help. pleasehelp patients that this drug could be helpfull for.

LDN as proved to be a safe and efficient alternative to many mainstream drug treatments. There is an abundance of clinical evidence already from those who have been on LDN, the treatment should either be allowed based on clinical evidence or trials should be conducted, but to ignore the significance of the treatment is criminal and if the system will not approve such safe treatments then the system needs changing!

Get the funds together for this drug .. you would want to try it if it was you with a life threatening illness...Thankyou

I am signing this to give our people a better chance of survival.

know what fibromyalgia is like

Legalise it!

Let's get this drug out there, people's lives at rsk

I have been trying unsuccessfully to be prescribed this for 2 years now. I have Lupus,chronic pain, hypothyroidism and depression. Having to take a combination of expensive medications when I really want to take this very inexpensive and seems the perfect solution to my long term conditions. Why is the NHS asking for more individually based care and asking us to take more control over our own health and well-being when they refuse to help us get better and save the NHS so much financially. This is such a valuable solution for so many issues to benefit so many

Save our children from dangerous immunosuppresants. Do the right thing.

Ldn is really helping with my MS... but with two young children and not being able to work as much, it's a financial burden for me every month. I'd love to see it trialled for these conditions, to help me and other people with these disabling illnesses..

This drug has given me my life back; long-term neuropathic rosacea sufferer! It has the capacity to help so many with chronic pain!

Keep it up

I want to help, being on lifelong drugs myself for my terminal cancer I know how important this is. Get signing now please x

This is so important, sign, share and let’s make a change!

LETS DO THIS

Struggling with symptoms of Hashimotos thyroiditis even though I am taking T4. There are loads of success stories of LDN when I research online. I don’t understand why the NHS is only interested in prescribing T4 when other drugs like this could help so much more.

So many lives could be improved by this and the cost of many wasted GP hours recouped

i AM IN PAIN AND NEED YOUR HELP

I have fibromyalgia.

Please fund research into LDN as it could help many people who live with debilitating conditions

I suffer with Fibo My sister has MS & my adult daughter has Chrohns Disease We all have limited life choices now & have children to look after.

If it helps people why not let it . Big pharma just want to make money from ill people enough is enough. We want to save our NHS give them the money rather than gifting other countries billions charity starts at home wasn’t we all told that in our lifetime?

hurry up please!

Hurry up ffs!!

I take this for hashimotos and RA. It needs to be licenced. Private prescriptions and the cost of medication puts it outside of affordable for the many who could benefit. It’s like a miracle to me.

It works

we need this asap , please !!!

LDN gave me back my life

I'm desperate to try this for my life debilitating fibromyalgia

I fully support this petition

This drug has been shown to have an impact on microglia cells and is one of the only drugs to cross the blood brain barrier to address brain inflammation. ME patients need this and further research on how to make it even better now.

This cheap, safe drug, with no side effects would help so many people and save the nhs so much money.

Let’s get this safe and very effective drug made available to those who can benefit from it now!

We all need to have access to LDN..

LDN should be available for all who need it.

Essential to get this medicine researched and available for sufferers of awful fibromyalgia pain when current medicine cocktails don't work. From a husband of a fibro patient.

I would like to support research into this inexpensive and low-risk treatment option for fibromyalgia. Despite taking multiple prescribed medications for this condition, and now addicted to opiates, I remain in pain and my quality of life continues to be affected.

As a carrier of 2 auto immune conditions(R A/ Hypo Thy) this could be 2 for the price of 1 in so many ways

I can see great benefits to the national health if they were to do the trials on This drug.

This drug would be a huge asset to the national health service

I strongly believe this drug should be available esp after being a Fibromyalgia sufferer for 12 yrs

UK especially is behind on this.

I would like the choice to use this a posed to Methotrexate

I have hashimotos and arthritis for.which this drug has helped both for many.

We need this safer autoimmune treatment available on the NHS please.

As a Crohns sufferer I whole heartedly support and encourage this

LDN would enable many people to get back to work! All the ‘invisible Illnesses’ that gps don’t know how to manage, could be helped by LDN!

I have rhematoid arthritis and inject mys of with chenoth

I have rhematoid arthritis and inject myself with chemotherapy every week which is the most horrible stuff and costs £1000's as apose to LDN!

I suffer from fibromyalgia, arthritis, bowel disease and a variety of other ligament and tendon related problems. I take high doses of opioid medication so I am very interested to see if this treatment might work for me.

Life saver, It saved my sons life ,the implant gave him a break from alcohol and a Life . With a country in an opiate epidemic and knife crime ect fuelled by it , it's a Scandal that it is so hard to access . Its not cure but a Miracle drug that could save so many lives.

I am about to try ldn. As my antibodies are 1300 so desperately wanting to get them lower. To help me recover

New Graves Disease treatments need research! 50 years with no break throughs! Fund the LDN clinical trial

LDN saves lives! Let us have access to it.

This sounds very interesting! As a fibromyalgia sufferer and on opiate style medications this could be a valid alternative!

ldn make me function normally, I am undiagnosed but have many related symptoms to MS and Fibro. We, people, could really benefit. My husband can work I can work without LDN we would on the social.

I have hasimotos and want to feel better with a better quality of life for me and my family. I want to try this to help with my symptoms.

Crohns small bowel 30years now spread to large bowel. Been through the meds now last resort Biologics ( no thanks) In all this time with many changes to diet etc have avoided surgery despite 30cm stricture. Really want to try LDN openly, instead find I have to skirt around the edges of the NHS to get it. Its my body let me choose. Fund the drug fund the trials Thanks

only been taking it a short while for sciatica and fibro............already seen improvements.

I agree ldn needs to be tested as could help many

This needs to be made available for fibromyalgia, there is enough evidence now and people who are living with daily pain should not be forced to buy it privately

Its high time this is made available to the vast amount of people in need.

Please please make this available on prescription. I have been on it 6 years its amazing many other drugs stopped working this was my life saver.

This drug must be funded for clinical large scale clinical trials for autoimmune conditions with view to licensing if benefits are found. This is cheap and generic, and has the potential to improve conditions without the huge cost.

I have chronic lyme disease and ldn helps me a lot on my healing journey

I use already LDM

"LDN is now a common treatment in Norway with over 10 thousand patients who use LDN daily. From the prescription register, we now know that 71% of Norwegian GPs prescribe and we constantly hear that LDN is also beginning to establish itself as treatment at Norwegian hospitals."

Fibro

LDN would help me and others who have several autoimmune conditions

Patients need this! Especially CFS patients who have no licensed treatments.

I really would love it more available for all of us with autoimmune diseases..

I live in France and I have been struggling with Hashimoto's disease for many years. My condition is sub-clinical and doctors in France have never prescribed hormone therapy or LDN for me. I would like to reduce the TPO antibodies and I have tried strict paleo diet and supplements and nothing cures me. Doctors in France are not familiar with LDN. I feel terribly tired all the time and nobody understands me. I hope this signature counts.

Very good initiative

LND has changed my life! It has given me back my life!

LDN works for so many people. Most of us have to buy it. It should be freely available for all, and proper trials conducted.

Because of LDN my autoimmune illness Eosinofiele Fasciitis is for at least 95% out of my body

Would like to try this for my eosinophilia fasciitis

we need this...

Very important this medication

Dit moet erkend worden, er hebben zoveel mensen baat bij.

Positieve dingen over gehoord

...

Done

I am a LDN user for a rare disease with great success. Totally totally believe in its great effect.

This drug is a life-saver for many illnesses and improves the lifes of many. The patent is expired so it's not profitable for pharmaceutical companies to do research. The government should start researching it and promoting it even though pharmaceutical companies are likely trying to stop this.

that it is prescribed without problems in case of complaints.

I used years of adictive painkillers because i have ME and fibromyalgia. Snce one year i am using LDN and it works like a treat. Lesser pain and no side effects. This should be available for everyone who needs it!

I have neuroborrelia and I want the late stage of the disease to be recognized. We are not psychologically ill as we are presented. We are really sick with symptoms and not hypochondriacs.

We need this to be available and know about

This is a life changing medication which does not harm those it doesn't help. Please help to make it available to others so they can also have their lives back.

40 Years without relive when a help was available, VERY BAD POLITICS

Let’s get this treatment on the road to help the millions who are suffering.