Seriously thinking about to start Dr. Wheldon treatment

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

Seriously thinking about to start Dr. Wheldon treatment

Postby MyChlamydiaAndI » Tue May 02, 2017 1:30 am

Hi everyone,

I just discovered about David's theory yesterday, and in a single day I got the most stunning theory I've read till now.

I got diagnosed last September, due to an Optical neuritis, and started the Copaxone 40mg treatment last January.

I knew my body did not become crazy all of a sudden, and till yesterday (and just through a 6th sense), I thought it would be some sort of Zoster virus, so I was already doubting into starting a Zovirax treatment by my own.

Yesterday I got enlighted through the ABC video. This brought me to http://www.davidwheldon.co.uk. I could not stop reading and reading, everything got sense, all the information was openly public and well referenced. Already for these facts, Dr. Wheldon, if you ever read my message, I'll be eternally thankful.

With a single day you gave me much more hope than in CEMCAT (Centre d'Esclerosi Múltiple de Catalunya) during this last year.

I haven't got other symptoms, but it seems I have new lesions on my brain (after the last MRI). I still do not fully understand what this means.

I am seriously considering to start the treatment, though, I would like to find a private Dr which could follow my case and help me to plan and understand my MRI's and blood results. As well, to plan a rich diet which will not allow the antibiotics to harm my inside.

How would I know that my Chlamydia is completely gone from my cells? Where could I test it?

Sarah, if you are reading this, thanks a lot to you too. :)

Sincerely,

Gisel.la Piñero-Casòliva
MyChlamydiaAndI
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Re: Seriously thinking about to start Dr. Wheldon treatment

Postby ElliotB » Tue May 02, 2017 6:45 am

Welcome to TIMS.


Just about EVERY theory/cure/protocolor makes sense and they all seem to work for some/many. I have read about the protocol but have not tried it. Please keep us informed on how things work out for you.



"How would I know that my Chlamydia is completely gone from my cells? Where could I test it?"

Have you asked your Doctor? Why wouldn't you just go to a lab and do a urine test?
ElliotB
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Re: Seriously thinking about to start Dr. Wheldon treatment

Postby MyChlamydiaAndI » Thu May 04, 2017 12:03 am

Hi ElliotB! :)

I did not ask to any Dr. yet. In the center where I am treated, they basically have not clue how to solve it and I feel their frustration every now and then. Besides, they already advised me that I would have to take the medicines they prescribed, and did not gave me much margin to have an opinion about it. Sincerely, I feel a bit numbered and tested every time I go there, so I am not really sure they'll want to hear any other theory.

About the C. Pulmoniae, I though it was much more complicated to test and just a few world labs had the technology to find it.

I will ask into my Pharmacy, where I normally take my blood results. Maybe they have the option.

Thanks a lot for your reply. Indeed, once I am ready to start it, I will keep a public track. (Hoping it could be useful for others).

Sincerely,

Gisel.la Piñero-Casòliva
MyChlamydiaAndI
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Posts: 2
Joined: Tue May 02, 2017 1:03 am

Re: Seriously thinking about to start Dr. Wheldon treatment

Postby SarahLonglands » Fri May 05, 2017 11:07 am

Hello Gisel,

I very rarely look at ThisisMS anymore, but something must have made me look today.

You seem a very intelligent person to understand the importance of the referencing on David's site, so you have a head start. The other thing in your favour is the fact that you live in Spain, where you will be able to acquire the right antibiotics much more easily. As to whether you will be able to find a doctor to treat you is another matter: here in the United Kingdom it is well nigh impossible now and many doctors have had there licence taken away.

Many people have been driven to treat themselves by buying to antibiotics from overseas and following the treatment schedule on David's site. People are doing this both in the United States and many European countries. A good site to look for people doing this and who will be willing to give you relevant addresses is here: http://tinyurl.com/5dyaw9

One more thing to say is that I started the treatment in 2003, finished it in 2007 and have not had an MS episode since then.

Send me a private message if you would like some more information.

Sarah
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.
SarahLonglands
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Location: Bedfordshire UK


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