I have just started Byron Whites AL Complex and have had some massive Herx's but I keep getting an Electrical sensation in my face,tongue like an electrical Headache with twitching, feels like my face/Head is charged.
It also feels like my body is kinda electrical and misfiring
I used to have this years ago before diagnosis but on this Byron Herb its very severe
Is this a die off - If so what bug can cause this as it literally feels like I am killing or aggrivating a bug HARD
Posted by elizzza811 (Member # 24713) on :
Not sure 'which' bug, but I've noticed a definitive correlation between the severity of my symptoms and solar/geomagnetic events like this one, and I've been checking this website daily for years now...
DODGING BULLETS: A magnetic filament winding around the sun's north pole untwisted explosively on Nov. 24th, hurling bits of itself into space. NASA's Solar Dynamics Observatory recorded the action in a movie entitled Lasso:
The eruption was not Earth-directed--polar eruptions never are--so no auroras or geomagnetic storms are expected as a result of the blast. Remarkably, the Lasso was just one of three filaments that erupted on Nov. 24th, all missing Earth. The other two may be seen here. With no filaments or sunspots directly facing our planet, the misses are expected to continue and Earth-effects should remain low through the American Thanksgiving holiday.
...I felt HORRIFIC (worse than just normal bad) Monday, Tuesday, Wednesday. Once these 3 filaments erupted though, I felt sooo much better. I had the first normal BM in months, my sinuses were open for the first time in years, just felt wonderful! Today I'm back to normal lousy though:-(
This could easily explain your electrical symptoms. It says it wasn't earth-directed, but I beg to differ with the effect it had on me. I actually had twitching things going on...mainly the left side of my face (cheek, eyelids)...when they hadn't yet erupted...
Posted by GiGi (Member # 259) on :
I had that sensation when I still had a lot of different dental metals in my mouth. I was also allergic to them. Full Moon and parasites also cause problems for many.
Hope you find the answer to feel good all the time.
Posted by Riannabri (Member # 25579) on :
It must be bug or toxin/herx related as I am herxing HARD on the Byron herbs and have not had it for years (I had this when 1st ill but not since) - so has to be related to Herx/Die Off or Bug
But yes it could be Parasite related as the Byron herbs also target parasites
Was just interested to know other peoples experiences
Posted by GiGi (Member # 259) on :
When you target parasites, you are releasing toxic metals because they store them. Be careful with reabsorption and redistribution of toxic metals.
Take care.
Posted by TF (Member # 14183) on :
You may be describing a mild case of trigeminal neuralgia. I got this when I had lyme. It usually affects only one side of the face. It is the 3-branch facial nerve firing, usually due to chewing or any other type of stimuli. It means lyme is attacking that facial nerve.
Google it and see if it sounds like what you have in the face. Mine was a severe electrical shock sensation that made me scream out.
If you want, you can try taking Benadryl to relieve the inflammation of that facial nerve. I tried many things (cranio-sacral therapy, etc.), and this was the only thing that helped.
If it gets really severe, you won't be able to stand it, and you will have to eat just soft things as chewing can set it off every time. Once it is set off enough, it just can happen at any time. Sure hope you don't get to that point. It can be a living hell.
Sounds like you are herxing on your treatment. Drink lots of water to flush out your system and eat lemons to cleanse your body also.
Hope you are over this very soon.
Posted by dali (Member # 24458) on :
I have a lot of twitching-dystonia in the face/neck area of my body. I also have been diagnosed with lyme. Chewing and clenching really sets it off. Facial twitching and other disorders of cranial nerves are not uncommon.
I am in treatment with antibiotics, but also take a small dose of clonazepam to calm the hyperexcitability of my nervous system. it helps although I do not like being on more pills.
I have learned to keep my mouth and teeth apart all day long. I also take alot of vitamin B and magnesium.
If this continues, see a neurologist. While they won't buy the Lyme idea, it doesn't matter, perhaps you can get some medication to manage the symptoms as you treat.
Good luck. I am doing alot better since I have been in treatment although I am not cured. But I am managing.
Posted by D Bergy (Member # 9984) on :
This has happened to my wife on several occasions. Both Lyme and Bart die off triggered numbness, nerve pain, weakness, and various other nerve related symptoms.
All of it has cleared up after these pathogens are reduced. I am speculating you will recover also, if you can reduce the infections. Only time will tell.
I think taking Coconut Oil may help repair any damage done. The fats may speed up recovery, and can't hurt in any case.
Dan
Posted by momlyme (Member # 27775) on :
Hey Dan, can you elaborate on how to take the coconut oil? I have a jar of virgin coconut oil and I make stuff with it... but is there a more medicinal regimen we can stick to? Not that I think my 11 year old is going to eat a spoonful of it... yuck!
Posted by GiGi (Member # 259) on :
Having been brought up with coconut oil, we put it on good bread, dark light crusty or garlic bread, anything; I like it well on thin all rye bread from Europe available in a number of stores here, just like butter, sprinkle a tiny bit of red salt on it and it tastes delicious. With some good bread, you can easily use a couple of spoons full. But I don't think I could swallow it down without something to go with it.
Try it, you may like it!
Best wishes to you and your son!
Posted by D Bergy (Member # 9984) on :
I have just taken a spoonful of it daily when I used it as a treatment for Crohn's Disease. Since it is a food, I do not think of it, or really use it as a medicine, but something to put into my regular diet.
Now, I use it to fry eggs in, or any other place where I would use some other kind of oil or butter. You certainly can use it in place of butter in many instances.
Nerve tissue and the brain in particular uses fats and cholesterol for repair and energy to function. If you use Turmeric for inflammation control, it is good to take it with any coconut oil, as it absorbs better this way.
Dan
Posted by Rianna (Member # 11038) on :
I truly think it is a die off, as my Herx's have been harder on the Byron Herbs than any Antibiotic
Strange you should mention COCONUT OIL as My LLND has me do this as part of an Phospholipid Exchange to displace toxic residues in the brain and to repair cell damage
I have to use the following daily:=
1 Dessert spoon or organic coconut oil 1 Dessert Spoon of Hemp seen Oil 1/2 teaspoon of sunflower oil 3 Phospholidy Choline (they come in a capsule but will blend)
Mix all together in a blender with water and drink
Here is her Info on it:-
Phospholipid exchange is a technique for supplying the correct proportion of fats and oils in a bioavailable form to replenish cell membranes and membranes within cells.
The basic membrane structure is made up of phosphatidylcholine.
Membranes then need the right proportion of omega 6 to 3 oils, i.e. 4:1. Hemp oil is very close to this ratio at 3.8:1. (Hemp oil is not the same as linseed oil!) So, add in a small amount of sunflower oil, say 5%.
The perfect fuel for brain cells is coconut oil, which is rich in medium chain triglycerides.
If there is poor digestion or poor gall bladder function for any reason then adding bile salts may be very helpful by further emulsifying fats and facilitating digestion and absorption.
Providing an abundance of clean oils helps to displace oils in the brain which hold polluting heavy metals, pesticides, volatile organic compounds etc. That is to say, these "clean" fats will displace "dirty" fats and also help detoxification
Posted by momlyme (Member # 27775) on :
Wow! Rianna, I would love to know where(or what brand) you get the phospholipid choline.
Any way to make this taste good? (I doubt it, but thought I'd try)