Seeking advice Cfs/Me and Emf sensitivity

Discussion in 'General' started by Davsey85, Dec 21, 2018.

  1. Davsey85

    Davsey85 New Member

    Hello everyone,

    My name is David

    I am new to this forum

    I am 33 years old

    I think this is a case of

    Cfs/me induced by emf

    About a year ago while working

    At delta airlines here in the atlanta

    Airport i noticed that i started

    Feeling weak in the break room

    Disoriented and confused

    Where high power microwave ovens

    Were running simultaneosly

    I started having muscle twitches

    As well everyday to this day

    Later that nignt it felt as

    the nuerons were on fire

    I had trouble sleeping and would

    feel very wired and tired

    Effects of radiation still stimulating

    The cns while the body was

    Tired feeling fried

    I would wake up the following

    morning and my parents footsteps

    And doors opening and closing

    started to sound lound.

    From that day on i believe that

    Is when CFS/me started

    I was still able to walk several miles

    A day in the forest and gradually

    Became less

    The more time i spent in nature

    Walking barefoot grounded

    I felt less inflammation and

    Muscle tremors twitching reduced

    The worse my emf sensitivity

    Became when i returned

    To the city as well as me symptoms

    Cars honking felt much louder

    Eventually i left the job

    Now i mostly walk lightly for 5-10

    Mins before crashing

    I have to do pacing to function

    Mother assists me with activites

    Of daily living

    I mostly try to avoid emf although

    It is difficult.Wifi and Cell phones

    Exposure tends to give me PEM

    where i am bedridden after a few

    hours of being in around public

    Cell phones or wifi. I also find

    That when there is sunlight and i am

    Outside this mitigates some of the

    effects and mitochondria is trying

    To heal.I feel like more threshold

    Before pem with the sun and trees

    Surrounding the roads in rural


    However my obamacare will run out

    In March and if i dont have income

    of 1200 a month by then i will not

    Have health insurance.I have yet

    To find a doc in georgia who treats

    Cfs/me and can give you a diagnosis

    My parents are moving to an

    apartment in march that has even

    More wifi and cell phones.

    There also leaving next week to

    Ethiopia and wondering if i should

    Go with them with 1600 left in

    The bank and unable to work due

    To cfs/me

    They are going for two weeks

    My goal for going there would

    Be to reverse cfs/me and emf

    Effects on wellbeing

    By the time they move into the

    apartment by march i dont know

    If i would get soc security soon

    Enough to avoid high emf

    I feel like i need to be in a low

    Emf environment to recover from


    I dont know by march if

    Would get approved for any disabilty

    Unless somehow an mri showed ms

    Or other nuero conditon

    The obamacare insurance docs

    I dont think believe in cfs/me

    Here in georgia as well as

    Emf sensitivity

    Same thing with ethiopia

    I may have to rely on sunshine

    And help from family to heal

    I have a sense that this is caused by

    Environment in my case

    Although i have an option to

    Get an mri to rule out MS or another

    Nuerological condition that would

    Qualify for disabilty.

    Not sure if i should take the risk

    And go with my parents to ethiopia?

    And try to regain redox as dr kruse

    Says being away from emf and more

    Sunlight although after 6 months of

    Money is gone and i stil have cfs/me

    In a tough job environment that

    would rough.

    In summary

    Living in the city around Emf
    -Pem if i walk much longer than 10 mins or around wifi/cell phones for longer than a few hours
    Q10 and bcaa sometimes help
    -muscle ache and pain
    -noise sensitivity-public restaraunts,
    Bars are intolerable (i think this is the ME part of the conditon
    everything seems loudetLr
    -sensory overload:tv seems overstimulating after a certain point

    Nuerologists just wants to prescribe

    On a sunny day driving shirtless
    In rural america symptoms feel
    Much better

    Although i sense that it would take
    Consecutive days/weeks to
    Regain lactate threshold and atp

    And reverse the condition

    I intuitively sense that is part

    Of the road back to healing

    Otherwise i am back to a cfs/me

    I dont know if chollera,spirulina,and

    Benonite clay can stop the root

    Of a cfs/me caused by Emf

    I think what i have is environmental
    Sickness syndrome

    With cfs/me you need someone to
    Help you while recovering in a
    Forest or quiet zone

    My parents are not willing to
    Stay with me in a quiet zone

    Nor anyone that i know

    Yet they are allowing me
    To stay with them in the city

    Which i appreciate

    Appreciate any feedback

    Thank you