Hi all new members :) Multiple Sclerosis and LDN

[LDNRT]

I'm Linda Elsegood founder of the LDN Research Trust, I have been taking LDN for over 10 years for Multiple Sclerosis. Does anyone else take LDN?

[katemtms]

Hi Linda, Fancy meeting you here! As you know, I have been taking LDN for the past six years for Multiple Sclerosis. Maybe we'll find some new people here to add to the conversation. You're looking good as always.

[LDNRT Partner]

Thank you, hate to say it but from you name I can't place you lol Let me know

[goatlady]

I am interested in trying LDN for lichen scerosis which is one of the auto immune problems listed that LDN is supposed to help. Have any members used it for this?

[LDNRT Partner in reply to goatlady]

I know of only two people and neither have agreed to be interviewed as yet, I will work on it. Good Luck

[goatlady in reply to LDNRT]

Thank you, if I can get my doctor to give me a prescription (of which he is hesitating even after reading info I gave him, I will let you know how it works for me.

[LDNRT Partner in reply to goatlady]

If you need help finding an DN prescribing doctor please let me know

[goatlady in reply to LDNRT]

Do you know of one near my area --northwestern New Jersey (Sussex County)

[LDNRT Partner in reply to goatlady]

Could you email me please? [e-mail]

[Oxymoron888]

I want to know what anyone, with experience thinks? I am seeing my MS nurse imminently and do not want to take any DMD’s for MS. I am interested in LDN, as I also have a Lyme diagnosis. Does anyone think LDN would be good for both CNS symptoms?

So much thanks.....