Re: LDN.... IN SOUTHERN CALIFORNIA

July 3, 2005

> Hello Just Leaving a Note For Any One In Southern California

> Searching

> For a Neurologist Who Would Prescribe LDN..I Am Taking LDN For m.s.

> (secondary chronic progressive) 1st Avonex Failed / 2nd Novantrone

> Did Very Little(Failed)....Neurologist is in Fullerton I am 99.9%

> Sure

> He Would Not Prescribe Over The Phone....Prescription 3mg filled

> At " Apothecary Options " CHICO, California. . . . Only 2 Months For

> Me On LDN So Far Not Helping. Will Continue For Several More

> Months..I

> Don't See Myself Ever Using The TEN THOUSAND DOLLER AND MORE Ms

> Drugs Again......I Post All This Because At One Time It Was Very

> Difficult For Me To Find A Doctor To Prescribe LDN..Unfortunately

> That's All To Common!!.....BYE FOR NOW.

==========

Have you tried 4.5mg of LDN? What is the filler being used in your capsules?

When you say LDN is not working for you, what do you mean by that? Are you

developing new symptoms never experienced before while on LDN? Are you

expecting symptom improvement from LDN that you haven't gotten? LDN's main

purpose is to halt MS progression, NOT improve symptoms. If one gets symptom

improvement while on LDN then that is an added plus, you got lucky. Since you

have gone through the strongest of MS treatments and if LDN is not halting you

disease progression at the 4.5mg to 6.0mg dosage then you need to get a Western

Blot test done to rule out Lyme disease if you've not been tested by this WB

blood test. Most doctors only do the ELISA test to check for Lyme but the ELISA

gives too many false negative results, the Western Blot is needed, do not settle

for just the ELISA. Dr. Bihari has had to use as much as 6.0mg of LDN with a

small few of his MS patients.

Recommended Posts