Chronic Head Pressure.. Please help me

What got rid of your head pressure? I have it along with ear pain/pressure, pressure in sinuses, stiff neck, sores on top of head. Worst symptoms. Other minor ones. I've been on Mepron now for 6 months. I was on doxy the first two months then switched to Bactrim. The first 3 I was on Zithromax then the last 3 I switched to Biaxin. My ART test showed my body hates Biaxin and it even hated Mepron but I am being kept on a 3 week pulse/1 week off with Bactrim DS everyday. I am also taking chlorella, cholestyramine, A-V, A-FNG, alpha lipoic acid, samento, pinella, vitamin D, salt/c c 12 grams, parastroy and olive leaf.

In Feburary I was making progress with the head pressure but since going off Biaxin and starting chlorella and A-V and A-FNG, my head pressure has been horrible. I cant run more than a mile without having a horrible burning sensation in my head.

I am losing hope. I had a positive Babesia Duncani test come back IgM positive, strands of lyme IgM/IgG, and IgG's for coxsackie, hhv-6, mycoplasma. I truly believe I have Lyme. HOWEVER, i have read horror stories about the Gardasil vaccine I got 5 months before my symptoms started.

What is in my head???

Hi...

I used to run 20 miles a week. I'm sure I got my bite whilst running :-(

My head pressure was my worst symptom.

I'm sure the running drove my lyme deeper. I also have babesia duncani and microti...lucky me



My head pressure flares if i run. Either die off or toxin related.

I'm treating my babesia with 800mg Artemisia Annua, Enula 60 drops (Nutramedix)
And having great success. No head pressure just occasional slight headaches.

I hope it eases soon, most definitely a crushing symptom.

I have a book that's coming out about benzodiazpines and z-drugs. What was hidden. Side effects from klonopin, (clonazepam) are what injured my central nervous system, made me sick and broke my immune down to bring these pathogens out of dormancy.

I was given the drug for broken sleep not anxiety and was told it was a safe sleep med. After I got sick from the drug, and then pathogens, I learned that broken sleep was pathogen induced.

So they gave me a psyche drug for the onset of pathogen infection which they didn't identify. I no longer agree with Allopathic Medicine after this. Allopathic Medicine is the mainstream = treating symptoms only. Hiding causes. Big $$.

I am very well educated on psychotropics now, and connected with medical doctors and activists that have the psychotropic drug info the mainstream med community doesn't learn. Pharma meds are not an option for me. I simply know too much about them now. Taking pharma abx's are a stretch, but I have to, to bring this down. No judgement for those who take the other pharma drugs.

My rapid thoughts are infection induced, not cortisol therefore not anxiety. Yolanda Foster has the overstimulation from the infection as well. Those that do not have this, always think it's anxiety and it's not. It's completely different.

So infection comes down, brain function goes to normal. I just write this so others that have it, are validated as it's again, not anxiety based. Completely unrelated to emotion.

But that said, "mom of 2 with lyme". I know you are trying to be helpful. I wish you didn't have so much on your plate and my heart goes out to you and everyone else.

Link for people of Yolanda Foster, David Foster's wife with the overstimulation that changes brain function, that give rapid thoughts. Not anxiety, or emotionally based but purely infection based; which goes down treating the infection. I have treated a year with plants but the plants wouldn't touch it. But plants cleared 95% of my body and head pressure and eye pressure.

On 2 pharma abx now for 2 weeks, and yes it's starting to target brain function so hopefully soon the overstimulation will end. I can actually feel the slow, slow change that will bring me out of chronic rapid thoughts. It's gone down 1/2 an inch in the last 48 hours finally.

http://lymedisease.org/news/touchedbylyme/yolanda-shell.html?utm_source=lyme+survey+%26+lab+testing&utm_campaign=survey+%26+labs&utm_medium=email

Good luck xrunner and everyone.

Post Edited (1runner) : 3/21/2013 11:11:13 AM (GMT-6)

Hi there,

I had mild but chronic head pressure and other head symptoms.

. I was sent to a neurologist (sent from Dr. J and Hansa Center) for an MRI. He suspected what is called CCSVI..chronic cerebro spinal insufficiency, due to lyme. It is when the veins, especially jugular, are constricted due to lyme.

They found I did have it. Both jugulars were constricted and blood was backflowing to the brain!! I had a procedure done, an outpatient procedure, that opened up the veins...a venous angioplasty. the pressure in my head cleared up during the procedure!

It sometimes comes back a little bit..but not like before.

I have heard (both on here and in person) of people having this vein issue with lyme disease and it resolving without the surgical procedure. I'm not sure exactly what they took.

I do know that lumbrokinase and buoloke and other enzymes can help..they digest the proteins/fibers that can cause the veins to constrict..kind of like a webbing or seaweed is in the veins from the lyme's disease.

If you google ccsvi, you will get a lot of info. It is very much worth seeing a doctor who knows about it to get treated.

email me if you want more detailed info.

good luck!!!

xrunner: just re-read your message.

Klinghardt knows about the venous insufficiency issue that I talked about (I am mentioning him because you are having ART testing done and he is the one who created ART).

The neurologist that I saw in Vegas takes his patients and is also his friend. So I would investigate the vein issue with your doctor or find someone who is knowledgeable about the vein restrictions due to lyme.

It is fairly common from what I have seen and heard. I know several people from Hansa with Lyme's disease who have had the surgical procedure and have heard of others still.

Yes I am close to Towson in Hunt Valley. Luckily my llmd is right down the road and she did it (Dr. L).

I have heard about that and will definitely look into it more. I am hoping and praying it will resolve on its own without surgery. We havent really gone after the Lyme yet with heavy duty antibiotics. I think this is actually my last month of Mepron before we hit it full force. I hope that will be the key for me.

If anyone knows of anyone who got it relieved with a specific antibiotic or herbal please let me know!

I know this is a year old but as I have been having pressure in my head on a daily basis after starting malarone and artemesinin for babesia this post came up when I did a search.

I am writing because the original poster's symptoms sound like Protomyxzoa especially because they mentioned the scalp sores. Protomyxzoa can cross react on tests and show positive for babesia duncani (only) on blood tests.