The tough question, the big question….When will I get better?
An LLMD tries to give a rough outline to that question
Even if you don’t think you have Lyme and have instead been diagnosed with Chronic Fatigue, Fibromyalgia, Lupus, Multiple Sclerosis, or any other auto-immune disease, you may want to give Lyme another thought….and watch this video
worth a repost, delicious!
On my way home from work I suddenly got a craving for turmeric ice cream. I have been making myself turmeric tea a few times a week (with some slight modifications): http://nourishedkitchen.com/golden-tea-turmeric-ginger-tea-coconut-milk/ So I thought making ice cream would be no big deal…and it turned out great!!
At this point put the above ingredients in your Vitamix (or comparable blender) and blend on high until turmeric and ginger are annihilated. Pour liquid through a fine mesh strainer to get rid of any sediment, then pour liquid back into blender and add:
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A shout out to Laurie who messaged me after reading my blog and sent me a link to this video. I have read some papers by Klinghardt before and knew how he felt about Electromagnetic field (EMF) exposure and the correlation to Lyme. But as this video suggests not only do Lyme bacteria thrive on EMFs, but so does mold. So if you’re suffering from biotoxic illness reducing your exposure to EMFs is also a must.
So it’s been a rough start to the year, aaaand it’s been a bit rougher the last 6 weeks, aaaaand rougher still the last few days.
So I posted (I think) about my body having been in a rougher state since a bunch of stress beginning of April…physical and emotional, med change, chemical exposure…But the past few days have been super rough with water retention and pain. Yesterday and today have been acute, super bad water retention and pain especially in my legs. Just sitting causes loss of circulation in my legs and feet and I have a lot of muscle and deep tissue pain along with “tingling/pin pricks” all over (my arms too but not as bad).
I had an event today that I was not going to miss under any circumstances. I was able to go and enjoy myself but had to try and ignore the pain in my legs and feeling they were so “tight” it is harder to bend them. My chief complaint is always my legs because they seem to be the most effected and painful, but my face is puffy and my arms are very swollen as well.
I am just wanting an end and an answer to this. I know there is something going on that is either getting missed or needs to be addressed a different way. I know this is my body overacting to literally everything, being “angry” all the time.
I am lying in bed right now doing nothing…feels like I ran a marathon. So far a more committed routine this past week of veggie juicing, 1 hour infrared sauna sessions and new anti yeast meds are either making me worse or causing a wave of herx misery, don’t know which is right.
Okay rant done!! Tomorrow is a new day. Hopefully I will find the magic spigot tomorrow.