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Dr Trevor Marshall
Research Team
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Posted: Tue Nov 11th, 2008 16:42 |
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Cool it, Deb. You must not abuse other members. You must respect their opinions and their experience.
You say "Guai is NOT palliative" yet when used in conjunction with the MP, at normal OTC doses (no more than 200mg every 4 hours) it is in fact palliative. It is one of the drugs which is useful to help control Immunopathology.
I hope you can finally find recovery with the MP. Well over 1000 have gone before you, and the moderators and advocates have a huge store of experience to draw upon. Please respect that.
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Chicago Deb
Member
| Joined: | Tue Jul 15th, 2008 |
| Location: | Illinois USA |
| Posts: | 18 |
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Offline
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Posted: Wed Nov 12th, 2008 17:15 |
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Stories of more docs going away from the protocol....
Oh it's just good old American capitalism, but they are really pushy. They INSIST they know what's best... and you can't push back, since they are often the only game in town. And if you refuse, then they have almost zero reason to keep you since they won't be selling you much.
Since I found a 2nd doc (who only suggested a vitamin IV for severe herxing) I'm ready to report the other doctor, but am still a tad scared of repercussions. He'll know any ramificatons came from me, since I'm the only patient who brought an encyclopedia of MP research and countered everything he said that I knew was wrong with a TM writing.
This guy is treating sarc with his version of MP.
I wish we could put out an email to every doctor on the list and kindly remind them that you are getting complaints and to remind them that maybe they could lose access to TM or anything to keep them in line, or rethink the ramifications of altering their approach.
I'm meeting lots of folks on MP and I keep hearing the same stories across the US about their doctors. I fear for them, as I remember walking home from my first MP doc and feeling so trapped and under his thumb. I allowed him to do a regular blood test, but purchased no other products and said I'd be back...yadda yadda.....and ran outta there.
I have one online pal right now, who is in this situation as of yesterday.
Use my page to talk to her, if you would. She's not feeling really good about the situation:
(She's the one who was reccomended a colonoscopy -and then a ton more vitamins-etc!..oh and the doc totally insisted on Klonopin)
You may not be aware: Doctors in the US just don't prescribe Valium anymore, it's just not done, unless it's post surgery.
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Fibro, OA. PH1 wk2 IP showing promise.
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Dr Trevor Marshall
Research Team
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Posted: Wed Nov 12th, 2008 18:08 |
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If you have had a negative experience with any physician who is on our list please send me a personal message by clicking on the "No New Messages" at top right of the screen, or by right-clicking on my name.
This is especially important if people are using "Their own version of the Marshall Protocol." Your message to me may well save somebody's life...
I think that one of the problems may be that so many of you are going to see "alternative" "specialist" practitioners. After our presentations in Portugal and the upcoming presentations in China, we really should be getting to the stage where your own physician should feel comfortable helping you.
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Chicago Deb
Member
| Joined: | Tue Jul 15th, 2008 |
| Location: | Illinois USA |
| Posts: | 18 |
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Posted: Sat Nov 15th, 2008 16:38 |
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Wow, my eyes are getting tired from all the research.
I'm printed most of it out and creating a book, to ease the eye strain.
But don't worry I'll get through it and perpare my abode long before start date.
Please, you needn't worry about me getting there with my respect for the work done by you, and I would never consider any alterations. So sorry if my US humor is taken in the wrong vain.
Last edited on Sat Nov 15th, 2008 19:23 by Chicago Deb
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Fibro, OA. PH1 wk2 IP showing promise.
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Dr Trevor Marshall
Research Team
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Posted: Sat Nov 15th, 2008 17:07 |
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There is no point beginning the MP journey unless you have read everything that Julia and the other moderators and advocates have suggested you read, and unless your focus and resolve is that the (long) pathway to cure is the best way for you to move forward with your life.
Most people who dropped out of the study did so because they could not cope with their emotional demons. I sense that you are really struggling. It may help you to take a look at the video we made after our presentations at the Karolinska conference on 'Cognitive dysfunction in disease' earlier this year:
http://www.vimeo.com/955029
The abstracts of our presentations there are listed and discussed in the Forum at
http://www.marshallprotocol.com/forum39/11385.html
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Chicago Deb
Member
| Joined: | Tue Jul 15th, 2008 |
| Location: | Illinois USA |
| Posts: | 18 |
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Posted: Sat Nov 15th, 2008 18:40 |
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Thank you for that info. very interesting, You get better with every speech.
Wish me luck. I'm having great progess with the eyes already.
A very good sign. The glasses work great too.
As per dropping out of this protocol. I'd love to show you my references.
I intend to be a stellar patient. You needn't worry, sir.
Love
deb
Last edited on Sat Nov 15th, 2008 19:13 by Chicago Deb
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Fibro, OA. PH1 wk2 IP showing promise.
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Chicago Deb
Member
| Joined: | Tue Jul 15th, 2008 |
| Location: | Illinois USA |
| Posts: | 18 |
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Posted: Thu Nov 20th, 2008 20:32 |
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YA-hoo, Im herxing away! Week 2 wtih the Benicar and I have the chills/sweats and cold like symptoms fatigue increased significantly. Rash with sores "some weeping" all over my face.
I'd had these symtpms for days, and refused to recognize them as anything but my bum luck that I had some weird acne this week, then hit the books and found out I'm right on target.
Sorry about no D number yet, doc is far away and since my face broke out and I wanted to tear my eyeballs out they hurt so bad with only one beni I took weeks prior to beginning protocol. That kinda gave Doc a good indication that I just might need this.
I'm very pleased and excited.
Thank you all
signature line preserved: Deb: Fibro, OA week 2 many indicators promising great progress
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Fibro, OA. PH1 wk2 IP showing promise.
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Dr Trevor Marshall
Research Team
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Posted: Thu Nov 20th, 2008 21:48 |
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Chicago Deb
Member
| Joined: | Tue Jul 15th, 2008 |
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| Posts: | 18 |
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Posted: Fri Nov 21st, 2008 17:23 |
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Ah life, very ironic. Just as I'm starting my jouney to good health...My older sister makes fun of me and refers to my quest as "Chasing Rainbows" by participating in this protocol. And that I should just get a real life and just try to forget about the Fibro and Arthritis.
But NOW: My sister, age 50, has just received a preliminary diagnosis of:
Histiocytosis Xanthogranuloma which, as I study this topic I guess it is now called Langerhans, or just LCH.
It was visible during a pelvic exam (very rare), she has no other signs that may indicate acute severe malignancy: no seizures or mood changes, no trouble with her eyes, or skin.
They shipped her off to oncology to figure out how far it's spread, if at all, and develop a treatment plan.
They made it clear she will likely be getting chemo and radiation for vag. legions.
I read somewhere that treating the legions that cannot be removed as cancerous cells was...well not the best way to go, but it's all oncologists have to offer, as this is such a rare condition.
She has none of the rash/papules, etc on her skin, as usually seen.
She believes she'll be dead in a year. I was hoping to burst her bubble and that maybe MP may work for this condition....depending on the test results of course and if she'll have enough time on the planet and drive to get better, etc.
Am I even in the ballpark of what MP can do? 
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Fibro, OA. PH1 wk2 IP showing promise.
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Julia
Advocate (on leave)
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Posted: Mon Nov 24th, 2008 16:22 |
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| Deb, the only way to tell if the MP would help your sister would be for her to get her D-Metabolites tested.
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Always consult a physician
Essential Info; FAQ; Julia's story
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