Nature girl treatment progress updates

I also still have migraines and pressure behind my eyes (kind of at the top of the eyes not behind)

I had a pharmacist compound Ergotamine and caffeine (if anyone wants the dosage let me know) that takes away the migraines

Also ice packs can help ----like ice hats

*hugs*

robby vieira said...
Igenex for Lyme will cost you $240 not $800.

just the Lyme WB IgM and IgG will run $210 (unless it recently changed?)

I was only positive for one bar each of long term and short term Lyme antibodies. But if you see a Lyme symptom list I check off on 90% of the symptoms. I'll tell you what a stress it is to be fighting something you're not even sure you have because the doctors say you are crazy

It makes it harder to believe I will be cured if I am worried I'm not attacking the right thing!!

But Avril's story comforted me I watched her interview on it and cried several times

Just want the cure

Thank you julymorning that meant so much to me I cried!!

I've been on the pharmaceuticals three weeks now (doxy the blue pill)

I've noted that while I'm still lethargic exhausted and depressed, (but not as badly) my other symptoms are practically gone. I noticed even my hands shake less. I get the barest of tingles in the pads of my feet sometimes a finger. Feels like a light blood swish. No longer do my hands and legs fall asleep at every moment. I even had my legs crossed by accident and didn't notice until I caught myself and uncrossed them!

So now I'm becoming convinced it's Lyme....but my cat wasn't cured from antibiotics she would get better then coming off them everything returned. So I'm waiting anxiously to see if I will be one of the people who says antibiotics cured them or not and if not ill work on a rife machine next and keep up my ozone as often as possible and Buher herbs and do what you said , work on my gut and immune system I've got deworming herbs ready to go just in case for those nasty parasite critters attached to the Lyme also msm waiting

Thank you sooooo much. I like the idea that I'm working towards healing I truly hope so

If I was to be cured somehow my next fear is reinfection as now I'm convinced tons of people have Lyme and don't know it ....ack

Post Edited (Naturegirl) : 1/2/2017 10:44:26 PM (GMT-7)

Hi everyone


I have been reading Bryan Rosners book and now I know why penicillin is not good for Lyme. It's because penicillin is a cell wall attacking antibiotic and that will not harm the Lyme which just converts into cyst and cell wall less form, and will make the Lyme more dangerous.

I'm done with the doxy and happy to say my symptoms are much reduced but still here. My symptoms are now mostly my eye still twitching, hands shaking , depression, and sometimes my hands and feet still tingle and go numb (last night a finger went dead and it was ouch)

My new path is this:

I have obtained some MMS .... will take some after letting the antibiotics leave my system and taking probiotics for a while

Am studying up on rife machines and will get the machine I can afford


Am not currently doing ozone. But it's still on the plate to do

Would like to find someone to hire (maybe off YouTube?) who can do a blood magnification for me with a black light microscopy

Discovered that the Marshall protocol is a rotating antibiotics treatment plan, investigating that

Still interested in the PAS drug that is curing Parkinson's

Found a doctor in florida who can test for coinfections with a staining technique, may do that and see if I have a co-infection


Learning this is a marathon not a sprint, just happy my symptoms are down


So much learning to do and things to try *sigh*

Thank u for. Being here with me

Post Edited (Naturegirl) : 1/25/2017 3:43:36 PM (GMT-7)

Thanks girlie

Sad to say my symptoms are still here tho much reduced. I'm off doxy now. I got some MMS have been taking that tho I haven't been able to take it every hour like they say. I feel it also herxed me at first now my symptoms do seem reduced but I still feel slight tingles in my arms and legs. Also now with the urge to pee constantly so I hope it's a UTI not that Lyme has eaten out my beta cells and is causing high blood sugar/diabetes

Feel very depressed like I'm falling apart

Keep falling and injuring myself too

Wondered if Lyme is the "old age" bacteria ?

Seems to give symptoms of old age

My hands aged

I got unstable and fall like an old person

Slight urinary incontinence

Weight changes cause saggy boobs never had that before
Looking older

Got strange bursted veins under my breasts

Etc

Also my friend who I think has Lyme and complains about his hands falling asleep keeps mentioning that he's just getting old so fast and his hands aged....very suspicious....


I have Bryans first book coming so I can get a good priced electro machine and start rifing soon...he does state never to use cell wall breaking antibiotics this will make Lyme worse;

He believes in rife machines antibiotics and has listed several cures like a salt cure the marshal protocol and etc

Just want to be healthy so tired of Lyme and sad about it too

Is Lyme an "old age" bacteria!???


Still can't figure out how to support my immune system

Feeling scared

Luv
NG

Post Edited (Naturegirl) : 2/15/2017 9:14:27 AM (GMT-7)

Sorry to hear of your frustration, Naturegirl!

After dealing with these infections for almost 3 years now and researching like crazy, it's my understanding that the health of the immune system is what makes the difference between those who are asymptomatically infected.....and those who are infected and dealing with symptoms - mild, severe or somewhere in between.

Dr. Bill Rawls healed himself from Lyme using Buhner's recommended herbs along with lifestyle changes. He recently released a book (Jan 2017) called "Unlocking Lyme". His writings really hit home for me.

He explains how herbs are very well-suited for treating these infections since the bugs are in low concentrations in the body. He also explains how herbs can help with healing.

Inflammation is what causes our symptoms. By disrupting our immune system, the bugs are able to cause that inflammation - this helps them scavenge nutrients.

We need to do things to reduce inflammation and heal the body. We also need to remodulate the immune system. There are many references to Buhner's research, writing and protocols that address these aspects of healing in "Unlocking Lyme".

In addition, Dr. Rawls writes about 7 categories of "system disruptors":

Unnatural diet
Toxin accumulation
Chronic stress
Artificial energy sources (computers and cell phones)
Free radical damage to tissues
Excessive or unnatural physical stress

Dr. Rawls firmly believes that restorative therapy (herbs, supplements, lifestyle changes) will slowly bring healing from Lyme.

Not surprisingly, there's much more to the book.

Here's some general info from Dr. Rawl's site:

/rawlsmd.com/health-articles/chronic-immune-dysfunction-lyme-disease

The $2.99 I paid for the Kindle version of "Unlocking Lyme" is the best $2.99 I ever spent. How I wish his book was available when I was first bit by the tick.

Besides my suggestion that you read "Unlocking Lyme", I also suggest that you add some herbs to help with cytokine remodulation/inflammation reduction (Buhner recommends Dan Shen/Red Sage and Chinese Skullcap and they are excellent).

Immune support is something else I suggest - Buhner recommends Cordyceps

Buhner recommends Eleuthero for fatigue and it's a great herb overall.

I take all of the herbs I just listed as well as the herbs you are taking. I also take Sida Acuta to help with twitches and Stephania to help with nerve issues...among the many other benefits both herbs provide. I'd say I'm at 99.6% and am very happy about that ;)

And, whether you read the book or not, I suggest you review the list of "system disruptors" and see if you can do anything to minimize them in your life.

Healing will come.

Just to chime in with a few of my own observations that correlate with others here.

Around 2008 I was given penicillin for an ear infection shortly before going on holiday to a tropical climate and I spent the first week feeling like I was dying. I couldn't stand up for a week and was bed bound in the hotel because of the pain of standing. Spent the second week loaded up on pain killers. Interesting how penicillin is mentioned here to agitate borrelia. Of course in 2008 I had no idea about lyme.

Secondly, 2006 (two years prior) I developed my second set of chronic symptoms around the same time I was really stressed with work and college and was dieting, hitting the gym pretty hard on top (now I know to be neuroborreliosis). Subtle loss of some sensation in my arms and legs (shooting electrical sensations) and numb big toes. I developed ejaculatory anhedonia (numb orgasm) and numb penis sensation as well. It just happened over night. I've never been an avid masturbator so I put these symptoms down to calorie defecit and extreme lifestyle stress. But again had no idea about lyme at this point.

Girlie said...
My hands are looking old too.... the bulging blue veins, the thin skin, the lack of collagen.

I'm sorry you're feeling down with this....it happens to me too...


(((hugs)))

Yessssss thank you..... what is up it's like every symptom is what we call old age....very weird.... I mean other than all these infections suddenly running amok in my body... ahhhh

Got Bryan Rosners first book what a waste of money it didn't give me any rife machine recommendations.... his second book is much better...still looking for a good machine that won't kill the pocketbook

Sorry for spamming
Just want to cry
I have garlic in my ear now
Tomorrow will make a garlic FEAST!

Feel terrified of pharmaceuticals right now but
I don't want to bash them;

I do have much lower symptoms since all these antibiotics

Even the twitch in my eye and tingling in my hands and feet is like 90% down

But now getting all these raging infections feel like I'm being eaten alive

Going to focus on natural cures again, glad the doxy seemed to help just scared 😳

Am also going to add:

3 raw vegan meals a week to diet (for enzymes, immune system)
Probiotics
Prebiotics
Take enzymes
Eat raw garlic again (I used to eat it almost every day no joke it was the base of all my food, and I was the bruschetta queen)
Take my macro and micro minerals

Read that immune book above


Any other suggestions to rebuild those immune cells in my gut would be ever so appreciated

Struggling not to cry

Nature girl here I couldn't log on and the system didn't recognize my email so here I am as nature girl 2!!

My post :


Hi sorry it's taken me so long to post an update

Some kind of hopeless feeling of avoidance of this

So I've tried just so much

Carnivora
MMS drops
Shilajit

And maybe more

It's hard to remember everything I have tried in desperation but it's not gone yet

Here's the thing, it's down much lower and or transforming

The tingles in my limbs is much lower but now sometimes it transforms into just aching and pain like arthritis omgggggggg

And fatigue wow 😳 like I'm an old lady who can't move

Well I'm cheerful about dying now heh

Don't care if I go ! Just don't want to be rendered homeless and still alive because of illness but if so I realized I will figure it out

Right now I am on an acidic campaign. I saw a doctor who says the opposite of all doctors who said I should look up the symptoms of being too alkaline. Called alkidosis. And the symptoms of being too acidic. Well due to my IC I cured I'm on a rampage to become more alkaline but after that bit of research I said WHOAH maybe I'm in alkalosis ! The symptoms are hand tremors and tingles and much more.

So I'm working to acidity myself a bit more these days like drink more apple cider vinegar. Not lemon juice as that actually turns alkaline in your system.


Wish I didn't have this but I'm gradually in acceptance now

Omg !!! I didn't know that!! Ack! Thank you girlie!!

Also I forgot to mention I came up tested with dangerously low vitamin d even tho I go into the sun routinely to bake the Lyme out
Just another Lyme marker

Also I had forgotten I could try that old tuberculosis drug PSA which has been curing Parkinson's

Parkinson's being Lyme by many opinions..... !

Naturegirl2 said...
Omg !!! I didn't know that!! Ack! Thank you girlie!!

Also I forgot to mention I came up tested with dangerously low vitamin d even tho I go into the sun routinely to bake the Lyme out
Just another Lyme marker

Also I had forgotten I could try that old tuberculosis drug PSA which has been curing Parkinson's

Parkinson's being Lyme by many opinions..... !

What drug is that with initials PSA?