GP

I just come from the visit with my GP. I went to ask him for some more blood analysis to check up the evolution.

Today he was especially friendly (and there was no one waiting in the waiting room), and so he listened to me about the cpn site. 

He said something as: "I have a friend which is really interested in all this, and they are discovering that antibiotics can cure lots of 'incurable or chronic' diseases."

I even had the chance to give him the URL and told him to check it out and explain it to his Dr friend. 

The feeling today was just fantastic. For the first time, someone (outside of this site) listens to me. :D 

And once again, Sarah and David... I have no words. :)

 

 

 

Gisel.la, now that IS good news!

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.

Gisela what wonderful news!  It’s the doctors we need to convert more than anyone else! :-) That is truth with a T! Last time I talk to Dr. Stratton, he said there was a lady, Nikki Schultek, working on creating a website for doctors. The link is https://intracellresearchgroup.com/ 

Trish

2003 Asthma diagnosis - 2004 took doxycycline per Dr. David Hahn work - asthma free. 2014 developed upper body myalgia/arthritis and asthma returned. Dec 2015 c pneumonia bloodwork IGG titer 1:512. Took 6 months of doxy for asthma flare up - again asthma gone but myalgia stayed. Dec 2017, extreme fatigue started. Emailed Dr. Wheldon. Research on cpnhelp.org - Jan 2, 2018 started Wheldon protocol.

Yes, it's good that there are some doctors that are taking a refreshing new look at how antibiotics might be used to cure a whole host of chronic diseases. It is a crying shame that if they look at this - our site - at this period in time, they will catch us with our pants down (metaphorically of course). Six months ago, this was a relatively easy-to-follow site. I hope that, like a phoenix, the knowledgebase will once again rise from this mound of ashes.

😭

G.

“Don't believe everything you read on the internet.”

―    Abraham Lincoln

The website is following its times and processes... just like someone under the Protocol. ;)

Pjdelambo... this website you showed me for doctors looks really cool too! :)

Now I just need to convince Mar, the Neurologist... I just need to think a good tricky way for her to listen... I was waiting for my Muses to send me an idea... when my mother appeared with a Book called:

Who is Who in Catalan Neurology - with a list of all the neurologists... I am stil trying to make a connection. It seems all their data and emails are there... 

Maybe a mass email under my name as an MS patient?

Sometimes I think I'll get dressed as a clown and start dancing in front of the hospital with a cartoon which says: 'Cure for MS here'... 

If you have any idea to bring their attention, it will be more than welcome. Meanwhile, I keep on thinking about the Mass email... or at least, an email to Mar... what do you think? If I end up into a Psychiatric House for this... I will need to you to come and help me out! :p

 

Gisel·la

(ONGOING PROTOCOL: 1 full year Protocol with 6 full Metro pulses)

MS Diagnosed: 21.IX.2016

 

Well... I did it. I just sent an email to Mar, I hope she gets it... 

I sent her both sites... The seed is planted. Let's see if it grows... ;)

 

 

Gisel·la

(ONGOING PROTOCOL: 1 full year Protocol with 6 full Metro pulses)

MS Diagnosed: 21.IX.2016

 

Thought it might be that!

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.

Thanks Boadicea! :)

As much info I can give them... much impact it will have... I just hope it works. :)

Gisel·la

(ONGOING PROTOCOL: 1 full year Protocol with 6 full Metro pulses)

MS Diagnosed: 21.IX.2016

 

I hope the GP and friend take good notice!

it was watching this, and the mention of the pathogenic cause of stomach ulcers that overcame any doubts i still had!

Jane

MS symptoms from 2001, DX RRMS in 2008, following, a change of hospital who sent me for an MRI, precipitated by some sight loss. Took Interferons, on and off. Prescribed  chemo infusions to slow pro

I hope the GP and friend take good notice!

it was watching this, and the mention of the pathogenic cause of stomach ulcers, that overcame any doubts i still had!

Jane

MS symptoms from 2001, DX RRMS in 2008, following, a change of hospital who sent me for an MRI, precipitated by some sight loss. Took Interferons, on and off. Prescribed  chemo infusions to slow pro

Mack, i’ve unwittingly reposted twice this morning! I’m sorry, it’s this hyperactive pisting finger if mine!

MS symptoms from 2001, DX RRMS in 2008, following, a change of hospital who sent me for an MRI, precipitated by some sight loss. Took Interferons, on and off. Prescribed  chemo infusions to slow pro