5 Apr 2019

NEWBIE- advice and experiences please! Protocol starting JAN 2019


Hi all incl Sarah and David! I'm new to here. Just recently weeks ago I was diagnosed with intermittant relapsing MS. Seemingly it all started in 2006 with optic neuritis then 2011 with lower limbs tingly,/ numbness. I have been started on daily Copaxen injectitions. But with a severely disabled child Im struggling both physically and mentally. Please help with advice as to how where, who, how much etc to get started on Wheldon Way of treatment. I believe in going in for the underlying cause rather than just band aid stuff. Thank you! Kiki Bojanic


Hi Kiki

how are you feeling now? Sonal has not been too good -- she puked a couple of days and was generally feeling low although she has receovered completely from shingles. But that must have taken its toll.

Yes corona is scary for all of us since many of us -- me certainly -- are in the high risk group -- age, hgeart issues hypertension, and yes MS is clearly not a healthy condition.

Take care, stay at home as much as possible. We are doing that in India as well. xxx


I am 76 years old. My daughter-in-law was diagnosed with MS and we are all very keen for her to start this new antibiotic treatment. We hope to be able to do this in the next couple of weeks by finding a doctor willing to deal with any issues like reactions that may crop up. My daughter-in-law is 43 years old.

I have been an active poilitical journalist most of my life and have felt for a long time that there must be a cure out there for MS which the medical community has largely ignored. I am very excited by the Wheldon protocol.

David smuggled in some nurofen for me at the start of the week and luckily I go home tomorrow. Sarah

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.