Chronic fatigue syndrome
Annette has had chronic fatigue syndrome, also known as ME, for over 25 years. She talks about how the condition affects her life and the things that have helped her to stay happy
Duration : 0:4:45
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July 3rd, 2009 at 9:58 am
Hang in there. I …
Hang in there. I hope a treatment will come for us soon. I’ve had CFS for 20 years. I feel your pain. Good video.
July 3rd, 2009 at 9:58 am
I know how you feel …
I know how you feel,I have been diagnosed with CFS too. And I have had it for about 7 months. I’m only 14 years old… And about everything is so hard for me… I miss out on so many day’s of school. Hanging with friend’s and doing the usual activities. It does affect your life severely. Alot of people have said to me that I am just a lazy . Although the pain I am I do not care what they think.
I hope the best for you Anette.
July 3rd, 2009 at 9:58 am
I did the raw diet …
I did the raw diet and free from diet for over two months with my doctors advice sadly it did nothing for me.(which i was really hoping it would be the magic pill sort of thing), Every time a new treatment or diet is recommended i’m first in line, but nothing up to now, but i’ll keep trying, anything ,anyone recommends.
July 3rd, 2009 at 9:58 am
I agree, i believe …
I agree, i believe its a food allergy problem. eg wheat allergies destroy the bodies abilty to absorb vitamins and minerals leaving you incredibly FATIGUED. Because its acting like a poison to the person they get all of the other typical CF symptoms such as a very bad stomach, total lack of energy, memory problems etc etc, your body just isnt getting the minerals required to operate correctly so it breaks down in strange ways. Good luck all
I THINK ITS LONG TERM POISONING.
July 3rd, 2009 at 9:58 am
Get off the …
Get off the pharmaceuticals and go raw vegan for a while!
Take a break to somewhere hot to get enough sunshine and go raw vegan.
Drugs just mask the symptoms.
July 3rd, 2009 at 9:58 am
You have a really …
You have a really good attitude & I know that helps a lot. I myself have Fibromyalgia, and I know that I have CFIDS/CFS/ME but I’ve never had a Dr. that believes in it. They say I have “chronic fatigue” but not “Chronic Fatigue Syndrome”. I live in the USA and although there are some doctors here that believe in the illness, the UK doctors seem to be more readily accepting of the CFS/ME diagnosis and more on the ball with treatments for it.
Take care and thanks for sharing your story!