Started David Wheldon Treatment today!!

A forum for the discussion of antibiotics as a potential therapy for MS

Re: Started David Wheldon Treatment today!!

Postby ElliotB » Thu Dec 21, 2017 12:18 pm

The Wheldon Protocol and the Coimbra vitamin protocol are quite different from each other and like all treatments/protocols for MS, work for some but not all. The Wheldon protocol uses high doses of antibiotics.

Google has many links available so you can get detailed info...
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Re: Started David Wheldon Treatment today!!

Postby orphansparrow » Tue Jan 02, 2018 10:54 pm

I'd like to bump this up with my question from before. Has anyone else tried this, and for those on this thread earlier - any updates? I'm very curious about this for my husband who is currently on no treatment but the Wahls diet.
orphansparrow
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Re: Started David Wheldon Treatment today!!

Postby SarahLonglands » Thu Jan 04, 2018 8:36 am

CPn Help.org is the place to start. Leave out the 'lite' and that is where you will find most people. We aren't much liked hereabouts, for some reason! Sarah

Leave out the capitalization and add 'lite' because the two sites are owned by different people and are not the same thing.
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.
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Re: Started David Wheldon Treatment today!!

Postby SarahLonglands » Thu Jan 04, 2018 11:42 am

Let's try again, but without the live link!

CPn Help.etcetcetc
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.
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Re: Started David Wheldon Treatment today!!

Postby SarahLonglands » Thu Jan 04, 2018 11:48 am

Whoever's idea it was to make all the cpn links misfire, ought to grow up!
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.
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Re: Started David Wheldon Treatment today!!

Postby Ella » Sat Jan 20, 2018 2:57 pm

Hi. This message is in response to Kittie and Orphansparrow:

I had my first MS symptom in 2000.
my second MS symptom was in 2007.
I was diagnosed with MS in 2011.
I used to have a lot of Pneumonia symptoms and lung infection prior to 2000.

I read the literature and did a blood test and found that my IgG levels for Chlamydia Pneumonae were high which shows I used to have the infection. My IgA levels were low meaning I no longer have Pneumonia. I was told by Dr. Stratton at Vanderbilt that if my IgG is above 1:64 I still have the bacteria in my system hiding and causing MS like symptoms even though my IgA levels are low. I didn't do a lumbar puncture which would have confirmed that I have the Chlamydia bacteria hiding in my system, based on Dr. Stratton's guidance, because my IgG was at least 64.

I started my antibiotic therapy in July of 2017. It has now been 7 months. One thing is for sure, I used to have an excellent and healthy digestive system and my gut bacteria did a great job. I have now ruined my healthy gut. That is a long term negative effect of the antibiotics which I will have to deal with after the therapy is over. The antibiotics also added layers and layers of fat to my stomach after about 4 months. I will have to deal with that as well.

The antibiotics I take are Azythromycin 250mg 3x/week, Minocycline100 mg 2x/day, Rifampin 300mg 2x/day, and Metronidazole 500mg 2x/day. These are based on Dr. Stratton's research and patented protocol to get rid of Chlamydia P. at Vanderbilt University in the US. Dr. Wheldon follows Dr. Stratton's protocol. However he is also a microbiologist and very knowledgeable in this field. Dr. Wheldon has a website which clarifies the Stratton research and protocol. He also has his own guide on extra supplements to take to support the liver while one takes the antibiotics.

Dr. Stratton used to start Metronidazole at the beginning of treatment with the other three, but now he suggests waiting at least 6 months to decrease the load of toxins that will be produced and therefore decrease the associated pain and symptoms. This antibiotic is the main one.

In terms of symptoms, I was guided to start it at low dose, otherwise it might be too painful during the die off of the bacteria.
week 1: Azythromycin for just one day a week
week 2: two days a week
week 3: three days a week.

Following this antibiotic, the pain I used to have in my sacroiliac joint disappeared for good.

Then I added Minocycline at 50 mg twice a day. several weeks later I increased to 100 mg twice a day.

Following this antibiotic, I did not see a difference.

Then I added Rifampin at half dose, and then increased to full dose.

The antibiotics caused nausea after a few months, but taking them with crackers helps.

By the end of 6 months, my gluten sensitivity which used to be extremely high improved by about 70%. It continues to improve.
By the end of 6 months, my brain fog was lifted.

I still have a lot of inflammation in my legs and my walking ability has gotten worst, which is to be expected. This is temporary. I will be starting the Metronidazole next week. I know that I will see improvements in several months.

In the end however, the demyelination of the nerves will take years to heal naturally. I plan to support the process with high grade Biotin 100mg 3x/day.

Good luck to both of you!
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