Admin please remove my post if not appropriate. In honour of Ann Boroch’s birthday today, many of us have adopted this unofficially as Candida Awareness Day.
Ann has helped thousands get their health back on track, getting out of wheelchairs and throwing away canes. Happy birthday Ann :)

I have had diagnosed PPMS since 1995, was in a wheelchair for 15 years, which is where I thought I’d stay, either that or bedridden, for the rest of my shortened life.
I had to have half my food cut up for me, blurred vision, slurred speech, horrendous food intolerances, 24/7 pain, spasms, fear and incontinence...

It never occurred to me to question the diagnosis rather than just accept my fate.
CCSVI treatment 2010 got my brain functioning sufficiently to work out what the hell was going on with me but sadly little else stayed at the optimum level.
I got rid of my neurologist, who only wanted to peddle pills anyway, and Googled my way back to life.

My symptoms not only fitted MS but also Candidiasis so I set off to fix the latter and would pick up the MS pieces when I saw what remained.

I chose the Ann Boroch Candida Protocol (ABP) which was the strictest I could find so had a chance of working.

The new diet removed alcohol and most fruit which had been my downfall - the candida don't care where their sugar comes from. I had been on the BBD for 11 years at that stage so not much else had to go. I changed all supplements to those recommended for healing the liver, gall-bladder, adrenals, leaky gut, thyroid and digestion, did yet another heavy metal detox, added some Biotin and upped my vaporised cannabis.

The symptoms I had June 2014 when I started the ABP were food intolerances, anaemia, low body temperature, cold feet, constipation, fruit cravings, cysts, abdominal distension, tinnitus, ear itchiness and ear ache, feeling worse with perfumes, fumes, tobacco smoke or dampness, spots in front of eyes, excessive tearing, itchy eyes, athlete's foot, itchy arches, swollen feet, toes and ankles, vaginitis, general feeling of unwellness, itchy scalp, sores on scalp, low blood sugar, IBS, Mitral Valve Prolapse, coated and cracked tongue, mouth ulcers, dry mouth, numb feet, tingling legs, almost no muscle strength, toe nail fungus, oddly-shaped toe nails, needle-like pain, arthritic-type pain, tightness in chest, shortness of breath, irritability when hungry, eczema, liver spots, white spots, sore throat, hoarseness, cough, spots on tongue, difficulty urinating, unable to empty completely, zero balance. If I could just get rid of a few it would be worth it.

The protocol is severe. I suffered 2 months of solid die off (Herxheimer reactions), my symptoms worsened, old symptoms returned, I lost a vast amount of weight that I didn't have to lose and felt dreadful. I had heard this was all part of the cleanse so I kept going.

After 2 and a quarter years on the protocol I have NONE of the above symptoms apart from one liver spot not completely faded yet and a leg that needs more rehab after so long in a wheelchair. I can walk 57 paces with 2 canes on my own, have sweated for the first summer ever, and my swimming is fast and powerful. I stand to shower alone rather than being dependant on someone to help me shower seated. I have heaps of energy and feel better than I did when I was 30. My life has changed for the better to where I never thought possible.

To have zero pain, fear, worry, confusion, spasms or any of that horrendous list of symptoms above it has been worth sacrificing sugar. I don’t miss alcohol at all (never thought that would happen), love my new food and shall always eat this way. In my opinion there is no healthier way.

If you too suffer even just a few of the same symptoms that I lived with for nearly 20 years, this could well be your answer. It isn’t easy but it is possible. If you wish to give it a try or are already following the protocol in isolation, I will be happy to chat you through it if you friend me. Wave goodbye to MS!

One leg still recovering from over 20 years of PPMS, 15 of them permanently in a wheelchair but other than that I have NO symptoms of MS after 2 and a quarte...