Comments on: Interview with P. Bear R.N. – Chronic Borreliosis (“Lyme”), MCS (multiple chemical sensitivities), Chronic Spinal Inflammation, Peripheral Neuropathy

By: P. Bear R.N.

P. Bear R.N. — Mon, 14 Sep 2009 19:11:14 +0000

You are most welcome Jane. It can be hard going but the the end point of improvement seems almost unlimited to me. Sadly I am no longer able to post on MP sites, but I am very much in favor of this treatment approach and continue to help people at Chronic Illness Recovery site.
best, P.B.

By: Paul Albert

Paul Albert — Mon, 14 Sep 2009 18:21:36 +0000

Hi Jane,

It’s good to hear you are hopeful. You have every right to be, and recovery typically takes several years. Recently, I put together a Knowledge Base article that addresses some of the psychological and social issues surrounding being on the MP. It might be up your alley. Have a look when you get a chance.
http://mpkb.org/doku.php/home:social

Best,
Paul

By: Jane McMillen

Jane McMillen — Sat, 12 Sep 2009 10:48:28 +0000

I am much encouraged by your testimony. I am on my 10th month of MP, but it has only been recently that I finally got my I25D down to a very low level. Am experiencing much psych and neuro IP, and struggle with the social isolation. I have seen improvement. Like you I am PTLDS patient and have 2 young adult daughters who have PTLDS as well. I am hopeful that when they see significant improvement in me they too will do the MP. Thank you!!

By: Amy Proal

Amy Proal — Thu, 26 Jun 2008 16:23:00 +0000

Hi Bob,

Hang in there! I’m impressed at your commitment to get your health back while working at the same time!

Best,

Amy

By: Bob

Bob — Wed, 25 Jun 2008 15:38:46 +0000

Great to read a success story to cheer me up. I’m in phase-2 of MP for Lyme, holding down a full time engineering job, and it has been a tough time. In the last few days, the herx has been killing me, therefore, it is timely that I read your interview today to keep me going.

Thanks,

By: P.B.

P.B. — Wed, 30 Apr 2008 19:24:47 +0000

Bev, I would contact the Marshall Protocol site to ask for their doctor lists.

http://www.marshallprotocol.com/forum11/11348.html
good luck, P.B.

By: Bevhg

Bevhg — Tue, 29 Apr 2008 18:39:47 +0000

PBear, I am so grateful to read about your progress–you give me hope. I put a message on the board a few minutes ago. I have been very sick for 2 years with 3 tick borne illnesses–babesia, bartonella and lyme. And I have so deteriorated that there have been days when I thought I would not live to see the next day. My doc and I tested for the 1, 25 D + it is high. Would love your advice in finding a lyme literate doc in CT, NH or Mass that has done MP. Thank you so much for posting your story. You do give me such hope. All the best, Bev

By: Pundun

Pundun — Sun, 30 Dec 2007 23:27:14 +0000

Good interview Amy.

So interesting to hear PBear’s story of his history of multiple allergies & sensitivities, then lymes. Great to hear of continual positive results with the Marshall Protocol. You give us all hope.

Pundun

By: Jeannine

Jeannine — Sun, 30 Dec 2007 22:29:21 +0000

PBear,

You are a great asset to the MP! Thanks for sharing your story. I find my “lyme doctor” to be doing the same as yours. I hope and pray that one day they will see the light! However right now I am greatful that he is allowing me to do the MP. It is people like you, amy, paul..all the members in fact, who will change the medical world…one MP member at a time…the word will get out.

Jeannine

By: Diana Pasley

Diana Pasley — Sun, 30 Dec 2007 01:35:50 +0000

Really great interview. I am so happy to hear of the progress PB has made. He has been through so much and yet keeps a positive attitude and outlook.
Bravo!! I hope to follow in his footsteps.