RE: FW: re 's response to my Post

[Guest guest]

Louise,

The same holds true with my mom. However, she was dx 10 years after my dx. Big difference being she does absolutely nothing for her MS, she is skeptical about everything. Unfortunately that attitude has landed her in a wheelchair! Louise I'm sure you've been reading the posts about MRI's that have been taken months after LDN and even the doctor's have been amazed. I'm glad your trying LDN and I look forward to your post after your next MRI! Good luck

(SPMS)

From: Louise de la Lande [mailto:ldelalande@...] Sent: Wednesday, May 12, 2004 8:25 PMlow dose naltrexone Subject: [low dose naltrexone] FW: re 's response to my Post

-----Original Message-----From: Louise de la Lande [mailto:ldelalande@...]Sent: Thursday, May 13, 2004 9:53 AMlow dose naltrexone@groupsSubject: re s response to my Post

Hi ,

Its because of the gap in mine and my mothers MS symptoms without any treatment whatsoever.So when I hear of somebody being having recovered for 15 years because of such and such a treatment ,Iam

sceptical.

I will only fully believe the LDN story when i see MRI's of all types of ms ( the 4 different patterns)

,as followup.

BUT i still take ldn, i dont love it ,but i want to see if these encouraging signs last.

Im sorry , I was brought upin a "Science "household ,studied it , andthat is a hell pf alot of conditioning

to get rid of overnight.

Its also quite useful at times.

Kind regards

Louise OZ