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Re: For Audrey re: LDN

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Hi Audrey.

Are you still in the U.S. or have you returned to the UK?

If you are in the UK now, did you manage to get onto an LDN

prescription? When do you anticipate starting lDN? Please keep us

posted on how you feel after taking it. All the best.

What type/stage of MS have you at the moment? Are there any other

types of alternative medications/treatments/diets/CRAB injections

that you have tried and found to be beneficial in reducing or

improving symptoms?

I have PPMS and am taking 6mg LDN now, like the few already in this

forum and it is helping me somewhat, and alot has to do with my frame

of mind to determine the best results.

Hope you get to start LDN soon.

Take care

Friday

--- In low dose naltrexone , Audrey Henry <mumpuss@y...>

wrote:

>

> I am living in U.S temporarily and I would like to

> start using LDN however I am moving back to the UK

> shortly and want to make sure I can get it prescribed

> overthere. Can anyone give advice about how I could

> get it prescribed or where in the UK?

>

> Audrey

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--- In low dose naltrexone , Audrey Henry <mumpuss@y...>

wrote:

> Hello Friday,

> I am PP at the mo and have had MS for 23 years.

> I'm 35. I live in the US temporarily.

Audrey: Were you 12 yrs. old when you got diagnosed?? That is so

young! Gail

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