Methods employed fighting ms I was diagnosed with the “slightly” frightening dis-ease called multiple sclerosis (ms). The initial tentative diagnosis came late 2015 which was soon followed with the label of primary progressive multiple sclerosis (ppms). This triggered a search for a cure for this dis-ease on my own since no neurologist was able to offer even the slightest glimmer of hope. Only thing in their offering was a wheelchair via a walking stick.

The search soon lead me to a couple of things:

    1. ms study by Roy Laver Swank and the resulting low fat diet which in now adopt to a large extent.
    2. Water only fasting.
    3. Keep a diary on what has happened during the dis-ease.
    4. Cling to God’s promises to us.
    5. Latest addition has been cardio exercise.
    6. CCSVI is something I’m taking a long hard look at as to whether to have this investigation done on me.
    7. Adding supplements to my diet after an extensive blood work was done on me at Antioxidant Clinics.
      • When looking at the cost vs. benefit I’m most likely going to cut down on the supplements and have already stopped drinking the neuro ice cube drink due to it’s horrendous price.
    8. Stem cell theraphy at Stem Cell Institute to see if anything could be fixed.

I got fed up when I last talked to my public sector neurologist and mentioned that the above methods have helped me, but I still have symptoms. This lead to diagnosis of primary progressive ms (ppms) and a response to to my question “what are our next steps?“; “well we will not do anything, but be sure to come and visit us again when your ability to work is impaired.” which to me was a bit harsh!

Due to this bleak attitude towards the people and their progress I decided to share my day to day struggle with ms and how I feel that I’m in control of the dis-ease instead of it controlling me.

The video that pushed me over my edge was:

What especially gripped me in this video was the blind trust of the patient Ron Smolders – I think he is now looking into CCSVI – in his neurologist to be able to stop the disease. Truth of the matter is that the neurologist just made Ron’s condition horribly worse!