Low Dose Naltrexone Testimonials for LDN Awareness Week

I created this video to inform the public about LDN (low dose naltrexone) and Awareness Week. Oct 19-25/2010

Category:

Film & Animation

Tags:

• Multiple sclerosis illness
• low dose naltrexone
• ldn reasearh trust
• hero
• doctors
• awareness
• testimonials
• Ebook
• Dr
• Mercola
• google
• Dr Birhari
• trauma
• linda elsegood
• diagnosis
• health

[22bellas]

than youim on ldn now and copaxone but am thinking if not taking it omg it hurts so bad

[edannajaynes59]

@22bellas There is a protocol to follow..you may have gone up too fast in dosing..start at l ml (liquid LDN) and stay there for 2 weeks going up in increments of .5 ml every 2 weeks until you reach the dose that is good for you..meaning no stiffness, headaches etc and your fatigue is gone..also you should go off the copaxone when you reach this level..I'll send you the protocol etc :))

[freespiritjustsoul]

Thanks for the great video!! You really touched me when you discussed the impact to your kids!! I'll start lDN as soon as I can get it-My doctor actually RECOMMENDED it to me :) Your word IS getting out!! Hopefully, because of your story, mine will be different! Much appreciation!!! XOXOXO

[edannajaynes59]

@freespiritjustsoul You are so welcome!! I had the Liberation treatment AND still take LDN..it saved my life..literally!!!. Many blessing and prayers to you for excellent health <3

[RingwoodLive]

I have been taking LDN for two years now for (so-called) Fibromyalgia - It is

the ONLY drug that actually helped and gave me my life back. Tried taking Tramadols round the clock, Lyrica, all manner of "natural remedies"

(Malic Acid etc). The sad thing is that in the USA so few doctors are aware and willing to try it.

[edannajaynes59]

@RingwoodLive I agree which is why we are doing Awarness week and a dvd of interviews..would you be interested? let me know :-) at jayne.thomas@live.ca

[SagDec15]

bravo, good video! :) 4/17/2003 is when I started LDN for MS. My dad was DX with stomach cancer 3/07, they gave him 6 months to live, we got him on LDN and he went into remission in 6 months, not the grave. My brother started 4/07 for sarcoidosis, he's back to playing softball, going on 59.

[enfermera72]

The testimonials were the reason I decided to try it, too. I've been on it 9 months. I am an LDN Aware advocate and I sincerely want to help those who need this medication. I don't want someone to deteriorate in health because they don't know about LDN. I only wish I would had known about it 4 years ago when I was first diagnosed with MS. Perhaps my disability wouldn't have been as severe had I gone on it in the very beginning. Please, if you take LDN, take a moment & share your story. I did!

[imnotabear]

It's still just a drug though, right? All of the conditions for which it is being touted can be treated with diet and lifestyle AFAIKT

[edannajaynes59]

@owlru oh, you are so welcome..I wish you all the best and if you need help getting LDN? let me know!! peace love and light

Jayne x

[owlru]

Thank you for the Video.( braver than I ) I have FM ( FIbromyalgia ) and nothing seems to be working,infact I feel I'm getting worse.LDN seems like a life-line I will be investigating .Your Video was clear and precise and I felt at ease listening to it,well done ! :)