Annoid! Considering treating myself.

Yes, I ended up treating myself once MD's and my LLMD were not able to get me well.

I went all natural, made a lot of changes in my life and I got well.

Do tons of research, read, and learn all you can about how to get the body strong.

And $200 is cheap, I hear some LLMD's are now going for $1200 a consult.

Sorry peace soul I meant 200 pounds but yeh I no they can be every expensive. I think I will carry on with the antibiotics until I feel no better and then I will consider the natural route. Thanks a lot for the advice KaliDhi but im not sure what a sliding scale is? You are lucky to have a doctor with so much experience. I am very sceptical about natural treatment I mean, can you actually CURE lymes with natural remedies?

I'm treating myself with all naturals. I started with a low dose of doxy, didn't like it so now don't use it. I am now slowly moving forward on naturals only. I have neuro lymes strong heavy on the Bart.

Yes you can heal from naturals. It's natural antibiotics. Antivirals, anti parasites, anti fungals.

Specifically for Bb, or Bart, or Babs too. Tinctures, some I have in powder for one herb for Bartonella and Bb tea though. My other separate Bart and Bb herbs are tincture. My biofilm buster and cyst busters come in liquid and one in capsule. I use and herb tincture that gets them out of hiding in tissue.

My herbs run about $100 per month, vits and supp over than. Say $150 a months.

There is logic behind the methods when you learn about it. And I have a strict alkaline diet, no sugar no carbs. Strict detox ritual. Daily.

I've talked and corresponded with plenty of people symptom free from naturals. All I did this last few months was research. I learned how the bugs behave specifically, their habits, and the treatment for it.

Post Edited (waverunner) : 4/13/2012 4:10:45 PM (GMT-6)

Oh Swashpro,

If one herbal supplement would take care of Lyme, wouldn't that be nice!

I can completely understand you wanting to take matters into your own hands. Your treatment options are very limited where you are living.

As others have pointed out, it will take a great deal of study on your part to do effectively. Rather difficult to do when you are not feeling well!

It would be very helpful to have someone else help you out with this. As you go through the healing process it may be difficult to gauge your own progress. Any chance you could find a naturopath who is willing to learn something new?

Grapefruit Seed Extract is also a cyst buster for lymes, and breaks through the biofilm

Lumbrokinase (earth worm enzymes), Serrapeptese (silk worm enzymes), Nattokinase (extracted from fermented soy, I hear it's weaker than the first two) do this cyst busting and biofilm breaking as well.

They break through the protection.

Teasal drives them out of hiding, those that are deep in tissue and joint cartilage etc. (Teasal is not just an anti inflammatory.)

I take my cyst buster and biofilm breakers and herb to get em outta deep tissue and cartilage hiding in the morning a bit before I take the herbs that git em. I have a cycle all day.

Once out of hiding, with no protection, you have an easier time eradicating the Bb, Bart, Babs with the specific herbs for them.

Make sense?

This is why eating dull food is what we have to do, they love sugar, just like yeast loves sugar. So many of us get those cravings for sugar and carbs which turn into sugar.

Break down their protective coatings, bust em out of hiding, kill em, and don't feed them lol. Git em!!!

There is a method. :) *I really miss my cheat day. In fitness I still had a cheat day where I had whatever I wanted. Waffles with syrup and extra butter, eggs benedict, pie, cupcakes with double butter icing, chocolate :(................. not in one day of course lol.

Post Edited (waverunner) : 4/14/2012 7:33:33 PM (GMT-6)

Swashpro what treatment are you on.After month of neuro symptoms and bones clicking after a recent stay in a tick area all my gps said i was crazy and it was in my head.

I Knew it wasnt.I then found out that my aunt had it and thats where i was staying in Dorset.Went BS and was diagnosed on symptoms and then my tests come back poss.Ive been 8weeks on doxy with small improvement BS are saying i need IV.I dont have the money to go BS anymore.

Took the results to 3 gps and there all messing me about saying we dont think you have it.Really messing with my future.My BS treatment has now run out and im stuck with no more money and no more treatment.How much do you pay a month for your treatment.It annoys me that BS said you need IV if you stay on doxy theres not much hope.

So angry i phoned them 2weeks back to get someone to ring me about other treatment methods.