I am coming out of a MCS flare at the moment. Many people have ongoing MCS flares, or MCS flares concurrent with multiple other symptoms. Being in pretty much full remission (aka zero CFS symptoms), I believe that sharing my observations as to cause, model, symptoms and treatment may help some people.
I am currently renovating our old home after it had been rented out for many years. For painting the exterior and interior, I had no MCS issues (defined as symptoms that persisted for more than 30 minutes after stopping an exposure). It was time to paint the interior and we hired someone to do the painting. They used a different brand of low VOC paint than what I had used for exterior and interior painting.
On my first visit to the house after the painting started, the fumes were thick because it had been raining and the windows had been kept closed. A slight headache which cleared after leaving. The next day, I awoke with a feeling of not wanting to go back to the house which I ascribed to not wishing to deal with the fumes. I decided that if I open up the house quickly and worked outside, everything should be fine.
It was, running some errands etc gave me breaks. About 6 hrs later, I started to do some electrical wiring in the house but on a different floor with windows open — there was no smell of fumes that I could detect .. about 45 minutes later I knew something was wrong. Initial symptoms:
- Stomach became very acidy
- Loss of focus, easily distracted
- Feeling off
Packed it in and headed home. Symptoms continue to worsen
- Whole body aches and pain
- Deterioration of cognitive ability
- Very easy frustrated
- Sore-raw throat
- Fell asleep on the sofa about a hour later and slept very hard for 4 hours
- Massive headaches across the front of the head
- Lymph nodes swollen in the neck
- Having mildly spice food cause a major over-reaction to the spice
- Usually, I have no problem with Extreme Hot spices…
- Sleep was disturbed — not just restless or difficult, but
- Many dreams that were very unsetting
On the first night after exposure, mild night-sweats returned, second night — major night sweats…
I am on the path to recovery. First item comes from lab tests done prior to and two weeks after a MCS episode of a friend. The marker for active coagulation went thru the roof (from high normal range (1.5 StdDev) to 7 standard deviation above the average — extremely high). Looking at the literature for allergies, you find that 30% of patients also have triggering of coagulation. This is definitely a part of MCS (and I suspect the main cause of many symptoms).
I proceeded with anticoagulation supplements:
- Fibrin Breakers:
- Aspirin (and the above)
These are effective in treating reducing many of the symptoms. These will be ongoing supplements because it can take days or weeks for the increase in coagulation to reduce. This then takes me to the second part of the model.
The sore throat and lymph nodes are typical reaction to an infection. IMHO, MCS is the detection of certain chemical in the blood system that mimics chemicals produced by some past infections. The body thinks that it has detected the infection returning and proceeds to defend itself, this includes starting coagulation to slow the spread of the (apparent) infection.
A second aspect is that the chemicals are likely chemicals that the prior infections used to farm the gut bacteria — hence the stomach upset as these chemicals triggers the residue amount of bad bacteria to go into overdrive! This response has the risk of the bad bacteria taking over — hence I proceeded to start pumping as many different types of probiotics into my stomach as I had available.
The third aspect is how to remove the chemicals from the body. There is a good chance that the concentration may actually be higher than that resulting from prior infections. I have learnt by experience that high fat food tends to reduce the concentration of these chemicals. One item, Olestra, is well documented as being the most effective substance to reduce PCB levels in the body. On a more humane front, brie and other cheeses will likely serve a similar function and is easy to test.
- Have some and see if you are feeling better 15 minutes later. If the answer is yes, then you may wish to blow your diet and go on a cheese diet — or be real brave and go for an Olestra Potato Chip diet (which Walmart usually carry).
The symptoms are reducing, Brie is not bad medicine! But until the chemicals clear out of the body and the activated coagulation calms down, it is working actively on reducing symptoms and encouraging the removal of the chemicals (and prevent re-exposure) on a day by day basis.
I recall from past literature that the reactivity of the body to an infection stays high for about a year and then slowly fades — which means that I need to minimize exposures to the same chemical for a year now that the body defense mechanism has been reactivated.
Please note that studies have found that sufficient chemicals can be capture by the moisture around the eye to provoke MCS. It is not a lung reaction — if the chemical gets into your system, even in very small quantity, it can provoke the immune system to believe that it is under attack…