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Proposal of LDN as a Research Topic
to HTA
Andrew
Barnett first suggested LDN as a Research Topic to the HTA.
The HTA panel
considered this suggestion on 19th Jan 2010, but their initial response was negative – see their letter to
Andrew HERE.
Several people
protested this decision, and we understand that HTA have agreed to reopen this
topic. We expect to have a further communication from HTA by 10th
March.
This was
our response to the HTA which we
submitted on 9th Feb.
We have now
submitted a second suggestion
to the HTA. This was submitted online on 23rd Feb and by email on 24th
Feb.
Our
Submission has also been sent by post on 02nd Mar along with an information pack on trials, research, clinical
experience, etc.
Please note
that the information pack is a very large zip file (approx 3.6MB) of a Word
document.
Since this
information pack was compiled and sent to HTA, results from further trials have
become available:
(1) Dr
Jarred Younger from
(2) Dr Jill
Smith has results from her Chrons study.
See letter that Bob Thompson
submitted to the Scottish Parliament Petitions Committee, and abstract from results
of trial.
Source for
the Abstract is:
Naltrexone Therapy Improves Activity
and Promotes Mucosal Healing in Active Crohn’S
Disease: a Placebo-Controlled Trial
(3)
Dr Ian Zagon’s email dated 15th June 2010 along with 2 of his
published papers. (Summaries already included in the information pack sent to
HTA). See below.
NOTE: Both
Dr.Jarred Younger and Dr. Jill Smith are currently seeking to have their
results published.
05th
March: HTA acknowledged receipt of email and package received by post on 04th
March.
29th
March: HTA advised us of current status
Our suggestion
“will be assessed in the period leading up to the June/July 2010 panel round
(29th June to 9th July).”
See further
follow up correspondence on the News page.
Dr Jarred Younger:- Extract from Report on the 2nd
European LDN Conference o 24th April 2010:
Following a delicious lunch, the audience
waited with baited breath for the much anticipated presentation from Dr Jarred
Younger from
At the time of press, Dr Younger was
continuing to analyse the results of his study in greater detail. We will be
able to bring you his indepth results as soon as his research paper is
published.
Dr Ian
Zagon:- Information provided to Jayne Crocker by email on 15th June
2010
From: jaynelcrocker [mailto:jaynelcrocker@
Sent: 15 June 2010 16:22
To: 'LDNforFibro@
Subject: Dosing Twice a Day - From Dr Ian Zagon
To put this matter to rest, I contacted Dr Zagon for his views on dosing 4.5mg
x 2/day and the below is his response:-
Dear Jayne:
First, LDN is an immunosuppressant - not an immunostimulant (as thought -
wrongly - by many).
Second, we recommended a dosage of 3 - 10 mg/day based on pharmacokinetics. 9
mg/day - getting to the edge but should be okay - this
person may not be optimizing her dosage however. Remember - you only want the
LDN working for 4-6 hr/day - the higher the dosage the longer it hangs
around and the shorter the time for your endorphins to work.
Third, stress has nothing to do with LDN.
Fourth, I am seeing some people who become tolerant to LDN and need to take it
once every 2 and some every 3 days. I can tell you that LDN
can work even as long as once every 4 or 5 days.
Dr. Zagon
Jayne Crocker
Further to my earlier email from Dr Zagon, I questioned LDN being an
immuno suppressant - please see his response below and articles attached.
Jayne Crocker
Dear Jayne:
We have a paper in press - Immunobiology - that B lymphocytes are suppressed in
cell proliferation by the OGF-OGFr axis - this is how LDN does its job. When
the paper comes out I will send it to you. We have another paper submitted
showing that T lymphocytes are also suppressed in cell proliferation by OGF.
Our studies under in vivo conditions are underway and stand in agreement with
our other results.
I have spent considerable time in these studies reviewing much of the flawed
investigations from past researchers giving the false impression
that LDN is an immunostimulant. There are papers suggesting otherwise – we have
nailed it down to the molecular level. Knockdown OGFr and OGF does not
work!!! Now, use your head - would you want more immune response if you have MS
or arthritis or lupus. No. This would make autoimmune diseases
worse. If I did not do so earlier, I will attach 2 papers on MS.
Click on LINK.
1. LINK Opioid growth factor suppresses expression of
experimental autoimmune encephalomyelitis (Zagon et al) available at www.sciencedirect.com
2. LINK Endogenous Opioids Regulate Expression of Experimental
Autoimmune Encephalomyelitis : a New Paradigm for the Treatment of Multiple
Sclerosis (Zagon et al)
Dr. Zagon
See
John Donnelly’s proposal on Your Country, Your Call. It got the most support.
Committed to saving
lives using LDN
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