LDN Info required

[Guest guest]

Great work! Go to www.remedyfind.com and look under Multiple Sclerosis, LDN is rated by users and stories told.

[Guest guest]

Dear Group

This is my first posting on the group, but I have been watching the

information with great interest over the last few months.

I have RRMS (a mild form) and have been on LDN for the last four

months and have had great success.

Before going on the LDN I had significant fatigue and heavy legs and

required a stick to walk. All these symptoms have now gone. I am

currently on 4.5mg per day.I am living in Ireland.

I was getting the LDN from Dr. Lawrence in Wales, and as a result of

my efforts his work load has increased significantly. We are trying

to get a clinical trial started in Ireland, and have had some success

in getting information on LDN to some neurologists.

Over the last four months we have succeeded in getting LDN in the

mainstream pharmacies and have also been able to get the MS Society,

mainly in the west of Ireland to give out information on LDN.

I have been asked to give a talk on LDN in January, 2004 and I am

looking for some information, both on the LDN and about people who

have been taking LDN. This will better inform the meeting. I am

expecting many questions about the future for LDN (especially in

respect of clinical trials, and recommended dosage). I am also

expecting questions of the effectiveness of the drug on the various

types of MS. Any help would be appreciated.

I feel that we have a better chance in Europe to get something done

about getting LDN into the mainstream. I have also been trying to get

a program on RTE (the national broadcaster) about LDN. It is slow

going so far. Once again any information will be of help.

Regards,

Joyce