Added: 4 years ago
From: ISSGOD
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  • found there may be a link between cfs and the antibiotics given to us as children ! your good bacteria becomes unstable and starts the problem with ibs ! look into it .

  • I am a recovered fibromyalgic who left the care of the medical profession to discover the cause and cure of this horrific condition without drugs, and am living proof you can cure this and take back your life. Symptoms are mistaken for the cause and treatments that help do not cure. Please, do not be discouraged by failed hope and keep going!!!

    Valerie Lumley, Recovered Fibromyalgic and author of

    "Curing Chronic Fibromyalgia - Choosing What Works"

  • Thanks for the Video. My CFS started 22 years ago with a case of Mono that just never went away. I did improve some at about 9 month markbut still feel like crud. My prayers go out to you and all people with this illness. I hope you get better!

  • God Bless. I'm 23 and have had it since 20. It's been 3 years and it hasn't gotten better...it hit me so hard. I hate it, but it's the way it is...bless ya!

  • hi robert,

    i have had M.E (chronic fatigue) since i was 8 years old im now 36 and still have it, i have been studying and writing about it for over a decade if you ever want to swap notes pls message me, comments for people are great but most people only suffer for a few years then regain their health, they are full of suggestions...hmmm, truthfully everybody is different if you want my view get in touch, take care sarah :-)

  • My CFS started with a flu too. I am so glad you didn't cut off your hand. Boy, I can understand how that almost happened, the brain fog from this dd is unbelievable and yeah, I wish we could just "snap out of it". I have a lot of respect for your decision to stop working there.

    We have to keep fighting to get CFS recognized as a truly disabling physical illness. I'm glad you're helping by posting videos of your experiences with it.

  • Robert,

    I have had CFS since 2002. My only salvation after my diagnosis was seeing a naturopath who put me through a major body detox. Change of diet, lifestyle and belief that you will heal helps. I am on SSD now for a year, but following alternative medicine has given me my life back. Be a seeker outside the medical community. You can heal. Read the Power of Now, Eckhart Tolle if you can, it got me through the tough times when I lost all from CFS.

    God bless.

  • I was diagnosed about 2 years ago, but suspect I've had it for at least a decade. I still struggle to work full-time. I use alot of FMLA and sick time. It feels like anyday my body will just shut down.

  • I was diagnosed about 2 years ago, but think that I've had it since 1999. I am still working full-time, going back and forth like a zombie. I rarely feel rested and barely sleep.

  • Read the book by Martha Kilcoyne called Defeat Chronic Fatigue Syndrome. It's only 108 pages, written for the CFS patient. She was ill for four+ years, housebound, went to dozens of doctors with no help, until she and her husband devised a strict plan of recovery which emphasized REST...10-14 hours a day. She got a sleep med to help. 3 years later she climbed Mt. Kilimanjaro!

  • You are not alone.  I've had it since January 1991, seventeen years. I'm thirty-eight years old now. I haven't been able to work in all that time. There are alot of us out there. Thanks for the video.

  • Thanks Suzanne and Englander, it is good to hear I am not alone, because I feel so isolated all of the time. I am looking into starting a support group in the Boise Idaho U.S.A. area soon. I just need to be around others that understand, so maybe we can find a solution together, because I have failed on my own.

  • Hi Robert, thanks for making this video. I've had CFS for almost a year now, and remember exactly the moment I first became ill. Like you I thought I'd be back at work in a few days but here I am, still unable to work a year later. Good to know things are changing for you.

  • I totally understand. I've had CFS for almost 10 years now. Thanks for posting this. Hopefully it will help to increase awareness.

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