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Natalie for CFS/ME Awareness

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Uploaded by on Apr 19, 2008

My scattered (in true CFS/ME style) run down & story of CFS/ME for CFS/ME awareness day (May 12). & yes, I was exhausted after recording this.

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  • Hello Natalie, Do you still have ME symptoms? I am currently feeling your described symptoms but yet to be diagnosed. I just want some hope x

  • @leannebell1 Hllo - I no longer have symptoms. I hope you are well

  • i also have m.e its mild i find ur story so shocking as i dnt get like that and worried now i just get very very tierd and ache all over i fight it all the way as i refuse 2 accept i am unwell keep ur chin held high

  • Pinkroxy - Don't worry, I know people that have had it 10 times the amount of time I have and always stayed at a mild level. Besides, I am about 90% improved now - so there's no need to worry! Especially as stress can make you feel worse x

Top Comments

  • theres a thing called the lightning process which is said to get rid of ME. i have ME too and in about a week im down to complete the 3 day lightning process course to hopefully *fingers crossed* get well again. ive had ME since i was 3 and im now coming up 18 :( cant remember what it was like to be normal so if this thing works, it'll be amazing :D

  • GOD bless u so much!! You are not alone in your battle!! God carries you in his arms <3

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  • Oh, soz, you have made updates, I didn't realise!!!

  • Hey Natalie, What do you think helped cause you to no longer have symptoms? I have had it 18 years, and am very interested to know if there is anything you think you did that helped your body to recover. Glad to read the good news.;-)

  • @ChronicFatigueSyn Hello - no I did not.

  • @ThreesecondHero I tryed LP and I regret it so much! They basicly get into your head that you yourself made yourself sick. They make you sign a "dont tell anyone any of the content- agreement". I advice people to think long before doing this. I know alot of people who struggels emotionally with a great sense of shame and being to blame for their disease. There is a BIG differense between taking responsebilty when deling with a disease and being to blame for!!!

  • @emodudes4life The 'lighning process' has no scientific basis and its effects on ME patients (or anyone else) have never been studied. It bears all the marks of a snake oil treatment. It is potentially dangerous for true ME patients, as are any programs that train such patients to ignore their body's warning signs and exert beyond their limits. I urge patients to read the warnings about the lightning process on ME/CFS patient boards before considering going through it.

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