Comments on: New Hope for Most Severe Chronic Cases of Lyme Disease! Part One

By: New Hope for Most Severe Chronic Cases of Lyme Disease! Part Three | About Lyme Disease

Thu, 01 Dec 2011 14:16:52 +0000

[...] New Hope for Most Severe Chronic Cases of Lyme Disease! Part One [...]

By: Building More Killer Cells For Chronic Lyme Disease | About Lyme Disease

Building More Killer Cells For Chronic Lyme Disease | About Lyme Disease — Mon, 28 Nov 2011 12:07:33 +0000

[...] New Hope for Most Severe Chronic Cases of Lyme Disease! Part One [...]

By: Kim

Kim — Sun, 18 Sep 2011 08:18:53 +0000

Just be aware, California does not allow it to be shipped into the state. Took it while in other places and felt better, but am taking serrapeptase and nattokinase until California gets with the program.

By: Jim Price

Jim Price — Sun, 11 Sep 2011 06:28:07 +0000

I was hit hard with lyme 5 years ago, no ins, and don’t trust the medical field at all. Did some research on line and found http://www.lymephotos.com. Followed the protocol and within a few weeks i was able to focus/concentrate again and some of the fatigue was gone, the pain wasn’t as bad and after two years the herxing stopped and i dropped down to one dose a day. Still have kinks in the neck sometimes and ringing in the ears all the time, but no more back,joint,lower jaw pain or heart block and no muscle twitches and i haven’t been lost or disoriented in about 4 years now. Anyone tired of giving money to doctors and drug companies should probably check it out. It’s only sea salt and vitamin c and it works for me.

By: Jenna Smith

Jenna Smith — Fri, 26 Aug 2011 12:19:35 +0000

Hi Kim – No, I never tire of encouragement from readers…it is what keeps me going! I am so glad I could help in some way. The info I have posted on the biofilm busters evolved as new information was released and if you look under protocols on the home website (not the blog) you will see the exact protocol I use now which I have to pulse because it is so strong. The brand of product is important and I make very specific recomendations on the website (www.LymeDiseaseResource.com).

I wrote 3 posts on the IVIG infusions – I’m not sure what you would like expanded on – if you could be more specific that would help. The infusions are prescribed by your doctor after they have evaluated your immune system with a blood test and found your immune system diminished, so the first thing to do is get your doctor to evaluate your immune system.

I am happy to hear that the Cat’s Claw had an immediate impact…another “super”supplement is GABA – I started with 750 mg caps as needed – especially helpful at night to help sleep through the pain.

Blessings,
Jenna

By: Kim

Kim — Thu, 25 Aug 2011 22:24:14 +0000

Thank you for your site (I suppose you’re tired of hearing that) and all you are doing. I started the Buhner protocol before I had the book because I was suffering too much with a single headache that has lasted since March of 2007. Being on Abx for the CDC’s recommended amount of time until I was re-tested and still positive for Lyme, my Doctor is more confident to keep me on Doxy for the last few years just to maintain some form of life in me. After just 2 days on Cats Claw, my “brain felt cool”. I knew we were on to something. I’ve added herbs as money permits and came across (somewhere) about the Lumbro/Serra/Natto information, and now, your blog. If I understand what You are doing, it’s 1-2 Lumbro 3x/day (my bottle says 40mg/600,000IU per tab.) 1-2 Natto 3x/day on an empty Stomach (my bottle says 150mg/3,000FU) and Serrapeptidase/Serrapeptase 40,000SPU/day (mine says 120,000U so it’d be every 3rd day or so, in your experience). For Herx you said you use 2 3x/day of Sarsparilla. You mentioned IVIG infusions would you care to expand upon what is involved there?

By: Jenna Smith

Jenna Smith — Sat, 18 Jun 2011 12:07:39 +0000

Steve,
Thanks for the great info! Very important –
Blessings,
Jenna

By: Steve Sponaugle

Steve Sponaugle — Fri, 17 Jun 2011 15:44:32 +0000

Disclaimer

I am not a Physician and this post should not be considered a substitute for medical examination, testing, diagnosis or treatment.

Nattokinase is safer than Lumbrokinase or Serrapeptase, since it’s anticlotting effects are moderated by Plasminogen feedback pathways. A Nattokinase dose of 2 caps, three times daily, can provide around the clock coverage.

Migraine sufferers frequently have highly elevated Thrombin/Antithrombin levels, at least intermittently. Lumbrokinase can dissolve the excess Thrombin and is especially helpful for patients with migraines, although it has a much shorter half life of about 2 hours. Lumbrokinase is usually more expensive than Nattokinase or Serrapeptase.

Serrapeptase is the most powerful anticlotting enzyme and is especially helpul for scleroderma and can also dissolve Lyme disease biofilm more effectively, than Nattokinase. Serrapeptase doses over 80,000 units for more than a month, have caused breathing problems in some situations. Serrapeptase dosages of 40,000 units daily, seldom seem to cause excess bleeding.

By: Christa G.

Christa G. — Tue, 29 Mar 2011 22:16:58 +0000

Hi, thank you so much for this article! I’m only 15 years old but got diagnosed with Lyme disease when I was in 6th grade. At first I got really sick (migraine for a full 7 days + throwing up + fever) then kind of bounced back but still with joint pain and headaches, etc. I am at a point right now where I miss at least one day of school a week because of not feeling well and being weak which stresses me beyond belief, and I am just trying to (and have been) find something that will at least help me a LITTLE bit. I have changed my diet and lifestyle not too long ago (eating healthy and exercising regularly) which helps a slight bit, but I still seem to have no energy especially when I get home from school. On top of that, I get a headache every day (not exaggerating) and I’m not sure why. A close friend of mine told me about a few different medicines to try (Lumbrokinase, Serrapeptase, and Venus Fly Trap Extract) but my mom doesn’t want to purchase any of them yet without knowing they’re capabilities and what they do; so I’m doing some research and I came across this! I was wondering if you could just give me some insight as to whether or not you think it would work for me, if I should try it, …I’m just looking for an opinion besides my own. Thank you so much for taking the time to read this! God Bless

By: Jenna Smith

Jenna Smith — Mon, 06 Dec 2010 19:09:33 +0000

Hi Fred -
I share in the overwhelming confusion that can paralyze even the most action-oriented person.

The truth is that we each have a unique case of Lyme based upon our underlying health conditions when we contract it.

You are not putting me on the spot, and there is nothing I would enjoy more than to steer you in the right direction. If she was on 2 years of abx then she must have had a Lyme-literate doctor who is important when you get in a bind. I take Cat’s Claw because it has verifiably raised my CD-57 but it was not enough on its own and now I am on IVIG infusions – basically rebuilding my immune system up from ground zero.

For your x-wife, I would recommend continued Cats Claw, Transfer Factor (http://www.dpbolvw.net/click-3278140-10374326target=_blank?url=http://www.houseofnutrition.com/admelatrfaba.html), Gold 360 (http://tinyurl.com/Gold360MB), and ApplePoly (http://tinyurl.com/applepolyMB) for building up the immune system; and then Himalayan salt caps (http://amzn.to/himsalt) and teasel drops (ladybarbara.net) to fight the infection…That is what I would do but I am not a doctor. Obviously you want to be very careful about allergies…I wish you every blessing and patience to find peace in this indescribable horror. You are a good man to return to your exwife in her time of need…I see so many men and women deserted by their spouses due to Lyme. God bless you!

Jenna