Low Dose Naltrexone LDN for Autoimmune - MS - Crohns - Cancer - Alan Geller Scary Diagnosis

[mrsardath]

Do you think that LDN could prevent MS before it is diagnosed? I was also wondering if you believe that toxins/chemicals have to do with having MS and I wonder if LDN has some invlovment in blocking some of these from getting to immune system?

[22bellas]

Is it sage to take Ldn while on avonex my dr gave me both it doesn't seem right but I diddnt get sick while on Ldn also felt better any advice id be thankful.

[mrsardath]

This may be a dumb question but is LDN like an opiate type drug in itself? Is that why everyone is feeling so much better because it has some sort of heroin-type properties? Because i thought when you are trying to get off heroin you take a drug that has low levels of heroin in it and is this the drug that their talking about? Thanks in advance :)

[MrDlt123]

I had my first MS attack 2 1/2 years ago and started on LDN almost immediately. I have been attack and disease progression-free since my first and only attack. I love this drug.

[AlanScaryDiagnosis]

@MrDlt123

Thanks for the post

Been 7 years for me!

Also credit other stuff including High dose Vit D and dietary changes

[MrDlt123]

@MrDlt123 These sound like the same changes I made. I cannot emphasize enough to people these change can change the course of the disease for them. Most ignore me in favor of the CRAB drugs that have little effect upon the course of the disease. I hope you continue to experience the same success. Cheers!

[lydibeau]

edit: I saw some with MS show the lessening of the outer third of eyebrows or even worse, meaning low FT3 and/or low IGF-1 which seem the sole reasons for it according to my hormonal wizz doctor. Is it both in MS or just low FT3?

[lydibeau]

wondering as I am maybe facing the diagnose of MS too, I saw MS is also low cupper and low zinc, both meaning diminished conversion to FT3 is taking place. Are they treating the low zinc, low cupper and maybe the low selenium too?

Is the low FT3 in serum or merely at tissue level?

I also try to connect some dots. I find it odd as cupper and zinc usually counterballance that in MS they both seem to be low. And what about IGF-1?

[morttodd]

LDN is a miracle drug.

fmy RA fibro CF & RLS have improved a lot or resolved. NO MORE COLDSORES, not even a cold!! I'm not on Enbrel anymore. My PSA went from 5+ to 0.7. MY GF's asthma & occupational dermatitis are much better on it. My dogs sarcoma is under control on it, he was paralyzed, in severe pain and cheyne-stoking yet much better in two days and fine now 6 months later An aquaintances shingles resolved rapidly. Google 'LDN and Cancer' and READ IT ALL

[22bellas]

does the no sleep go away jus started ldn took it for 1 wk 1mg couldnt sleep so i stoped taking it now i feel im having a attack so i took my avonex shot to try and wake my legs up thanks

[AlanScaryDiagnosis]

@22bellas - In my case sleeplessness was about 2 weeks and that seems fairly common. I never used Avonex so no comment there. Some take up to 6 mg of LDN during exacerbations - I have been attack free since starting LDN in 2004 although I do lots of stuff in addition to taking 4.5 mg of LDN nightly.

[ladidiaz]

Thank you,thank you,thank you..Ive had Rhuematoid arthritis for over 7 years now but I believe ive had it since 17 and i am now 45..with no health insurance. I`m greatful to you for this information and will strive to heal myself naturaly..may the creature continue to bless you and your family.

[morttodd]

@ladidiaz

I was in the same boat as you. Please consider LDN, buy it online if you have to or from mexico costs maybe 10 cents a day. I was dying, unable to manage and my rheumy was out of options with my meds maxed out. I saved my gf's life with it, my dog and another persons dog too, so so much for any placebo effects, the dogs dont know theyre taking anything.

[notapplicable66]

LDN has stopped working for me since I am in a relapse now. I have been taking 4.5 mg's once a night. I have been taking LDN for over 3 years. I had one bad relapse during the time and I upped the LDN dosage from 3 mg's to 4.5 mg's. I guess my body has gotten too used to the LDN and I have no choice but to go on a MS drug now since funding for CCSVI has stopped.

[AlanScaryDiagnosis]

@notapplicable66

Sorry to hear your are not doing as well. My understanding is that most take LDN at 4.5mg as a norm and some go to 6 mg or more when having an attack. It might be worth doing some additional reading. I believe the CCSVI work will continue and also believe that it will prove helpful for many.

[kkkkkkatherine]

Alan,

I am considering LDN for my MS. Are you aware of the HUGE revolution in MS treatment CCSVI, LIBERATION based on century old theory of MS being a Vascular Issue!

Love your proactive stance in self care!! Thank you!!

[AlanScaryDiagnosis]

Thanks for the comments. I did another youtube on CCSVI and have 2 more I need to post (one on some "Plain Talk about CCSVI" and the other on CCSVI: IS IV Chelation a non-surgical option?). Although clearing out the arteries and or repairing any malformations might be a short or perhaps longterm fix I believe LDN is benign enough and the risk reward great enough that I will be staying on LDN even if I am a candidate for CCSVI. I plan to get tested once proper testing is generally available.

[rooflee]

I love this video. I'm ordering Naltrexone 50mg generic from an online pharmacy today. I plan to dissolve it in distilled water to easily measure out 3mg doses. I will let you know how it helps with my girlfriend's fibromyalgia. Peace. (P.S. did anyone ever tell you you sound like Kermit the frog? LOL :))

[willyhillydude]

@rooflee Hello.If you don't mind I'm curious to know whether or not you have a prescription. I think i would benefit from LDN but I don't have medical coverage at the moment so getting a prescription is hopeless.

[cwcw111]

good vid well educated, you should be a doctor it would be easy listening to you ,,,thanks for sharing,,,,,,,regards

[smithcd77]

Good for you!!! My son has autism and this is a very popular drug for our community as well. My mother in law has MS and has taken a turn for the worse. Hoping she will try this.

[notapplicable66]

Are you also taking interferon? Interferon slows down the immune system. I take LDN only. LDN increases endorphins and also increases T-helper cells.

[AlanScaryDiagnosis]

Just LDN for me. Opted not to take any Standard of Care drugs. I do supplement heavily with fish oil, D3, B12, etc in addition to detoxing and using some homeopathic stuff. I am also a big believer in Leafy Green Shakes (Vita -Mix).

[notapplicable66]

In the winter I take 4,000 iu's of vitamin D. Then I reduce it to 2,000 iu's during the summer. I also take Omega 3 and Vitamin B12 the Methylcobalamin form. The body retains it better, it supplies energy, and it helps promote myelin repair.

[BuggedbyMPD]

Very nice video. Thank you.

[savingbeauty]

Fantastic!!! After 3 years the same results. Dr. Bihari - founder - has had over a 90% success rate. See "LDN Documentary" video.google. You will notice that LDN users are calm, collected and full of hope on YouTube!

[AlanScaryDiagnosis]

Thanks for the comments. Glad to hear you are doing well as well!

[AlanScaryDiagnosis]

Reports by users (and my personal experience) focus on reducing or eliminating progression rather than LDN addressing old symptoms. Having said that some report improvements in symptoms from "recent" past attacks. I suggest a look at the LDN website (linked on my site) and a visit to User Groups (like LDN - YAhoo Group) and searching their archives for specific information on Behcets and LDN. I hope this helps! Best Alan

[lizzy890]

Oh and I just had to mention that you have a very beautiful home!

[AlanScaryDiagnosis]

Thanks - we know how very fortunate we are!

[tmmylopez]

I got diagnosed with Neuro Behcet's one year ago. My left leg went weak and bowel and bladder problems, you think LDN would help get these functions back?

[savingbeauty]

Better to keep open about LDN potential. It certainly takes care of old symptions - I am a 21 year sufferer - and acts as a foundation to be positive and use the mind to go further on the course to recovery. EFT is incredible if used correctly. There are other treatments and LDN does not interfere.

[lizzy890]

This is something I will definitely bring up to my neurologist when I see him.

I'm 19 years old and have been diagnosed in 07'. I wish I was as proactive as yourself and many others with MS but instead I choose to stray away from MS related subjects only because I become overwhelmed, anxious easily.

Some of the newest MS youtube videos including yours has definitely inspired me to alter my diet and become a bit more active. I don't want MS to take over my life anymore.

[AlanScaryDiagnosis]

It is really important not to be passive & submissive about MS or any disease or condition, especially the so-called degenerative ones. MS for most means "attack"s that result in loss of functionality - reducing or eliminating those attacks becomes the name of the game. At 19 it's crucial you become proactive trying stuff & staying current on choices. YOU are one of the reasons I wrote "Scary Diagnosis". Diet, supplements, drugs are choices today. Stem Cells are looking very promising- tomorrow.

[Helilondon]

Alan, thank you very much for posting this on youtube. Unfortunately, there is not much info available on youtube about LDN. Thefore your video is very helpful. Anna & Albert

[AlanScaryDiagnosis]

Thanks for the kind words!

LDN is a fascinating story & I now know several people taking it for a variety of issues (Colitis, Cancer preventative). It is my favorite chapter in my book and is always part of any public speaking I do.

The reason I wrote the book & doing these videos plus speaking publicly is that I have seen personally how getting out there and being vocal can change things. It's only little bits at a time but every bit helps. The LDN group in the UK is certainly an inspiration.

[watzgoodinthe718]

question do you use the swank diet;;

and are you wheel chair bound and are u able to still work???

[AlanScaryDiagnosis]

I do use sort of swank and Best Bet in that I eat mostly veggies and meat (I know that isn't recommended) & avoid most grains. Everyone is different and needs to do their own trial and error food wise. I supplement heavily & chelate.

I am not wheelchair bound and in fact still play golf. I semi-retired when I was very symptomatic (5 years ago) and in addition to the book I write articles and speak publicly. My second book is already in the works and have plans for a 3rd with my Osteopath.

[watzgoodinthe718]

Excellent just excellent!!!!

LDN is the future... pharmaceuticals just want big money..

this world is a sad place