LDN board purpose

[Guest guest]

There is a heavy incidence of MS users on the board, but I have no complaint. My interest is in treating my wife's cancer. I simply put a filter on my LDN list emails so that I receive only those with key words of interest to me. I occasionally turn the filter off for a couple of days, just to keep up to speed with the general conversation here. I view it as my job to filter what's important to me. It does seem reasonable to keep LDN as at least part of the subject of each thread if not every post.

A merry heart doeth good like a medicine: but a broken spirit drieth the bones. Proverbs 17:22 Don Schultz (no medical training, and not terribly bright)Near Joliet IL. Husband and Caregiver to Barb Schultz, born '49Dx'd June/01; IgA Kappa @5,880, B2M 7.8, Radiation to L3, Aredia 6X now Zometa monthly, 100mg Thal daily & 40mgX4days pulsed Dex thru Dec '01 when failed; Mar-Jun/02 2 rounds VAD no effect & 2 rounds DTPACE modest effect; autoSCT July/02 full remission in Sep/02. Interferon maint' Aug/02 to Jan 03; Jan 03 IgA climbing; Feb 03 Hi dose Dex Failed, Velcade Phase3 trial Mar/03, IgA down 99% after 2 cycles, After 8 cycles of phase3 trial IgA below normal. Dec/03 now in 2nd Continuation phase, M-spike 0.1 and still going down!, 1 liter saline minimizing fluish side effects. Taking DFCI supplement regimen to minimize Velcade PN.Blessed be the Lord, who daily loads us with benefits, even the God of our salvation. Selah (pause, consider this) Psalms 68:19http://www.labtestsonline.org/http://www.myeloma.org/http://www.multiplemyeloma.org/http://www.escapepod.com/myeloma/Abb.html (abbreviations)

----- Original Message -----

From: I AM CANADIAN

low dose naltrexone

Sent: Thursday, January 08, 2004 9:48 AM

Subject: RE: [low dose naltrexone] "ASPERTAME"

True I understand that I just don’t mind hearing about what works for people with immunity etc… a lot of people talk about vitamins and supplements that seem to help through flu season etc… I found that helpful. And I can understand people here with other medications feeling everything is about MS and we’ve lost track of LDN that’s understandable too.