Chronic Fatigue Syndrome Support Group
Chronic Fatigue Syndrome (ME/CFS) describes a sense of exhaustion and post-exertion malaise, even when you have gotten enough rest and sleep. The disease is characterized by six months of incapacitating fatigue experienced as profound exhaustion and extremely poor stamina, and problems with concentration and short-term memory. The cause is unknown, but it is a...

I have only watched half so far but I like the use of Post Exertional Amplification of Symptoms VS Post Exertional Malaise.
Will finish it later but look forward to having my hubby watch it with me.
I just love Youtube, what a great resource it is. And I'm so thankful for people like Prof. Van Ness who give us hope and support.
COULDN'T watch all of it at one time, not could
But that's a tall order, nobody here would give out an email address to me when I asked for one. All they really have to do is search Youtube for Prof. Mark Van Ness, but that's a stretch too.
I found the video by searching ME/CFS on Youtube. There's a lot of good info out there...easily found with Google and Youtube searches.
My local doctors told me that all the information on the internet is false and misleading...LOL...really they did! Just believe what we tell ya' kid and you can't go wrong...LOL.
But maybe the rest of the country has better doctors, I don't know.
After the film, Prof Mark VanNess spoke about the work he and his team are doing at the fatigue laboratory in the Health, Exercise, and
Sport Sciences Department, University of the Pacific, California.
Working with people who have mild to moderate M.E., they are finding objective, rather than self-reported or subjective, evidence for the kind of fatigue that is specific to M.E.
Using cardiopulmonary exercise testing, Prof VanNess has proven that people with M.E.:
experience significant post-exertional malaise, though he prefers to call it post-exertional amplification of symptoms
have significantly impaired ability to generate energy from aerobic activity.
The key is that subjects are tested over two days. People with M.E. and healthy controls, all volunteers, spend 10 minutes on the
treadmill on the first day, and then again 24 hours later. Results show that on the second day the metabolic function of people with M.E.
has dropped by around 25%, such a marked decrease that, Prof VanNess told us, exercise physiologists protested that the machine
must not be calibrated properly.
As a result of the data he has gathered, Prof VanNess has concluded that therapeutic interventions for people with M.E. should avoid
aerobic exercise. Instead, they should be offered analeptic activity, intended to retrain the short-term (anaerobic) energy system to
increase range of motion and improve functional strength. Crucially, he said, the ratio of activity to rest should be one to three, and
physical therapists should be trained and experienced in this type of physical therapy.
I pasted this from the Online ME Center of the Action for ME organization. The film they're referring to is "Voices From the Shadows".
I'll reiterate...this is not about curing ME/CFS, it's about giving us significant improvement in our quality of life. I personally decided years ago not to sit around waiting for the medical/research community to come up with a cure...I believe in making the best of the situation as it exists.
I sometimes take three 20 min. rest breaks in one morning of work. It helps keep me hydrated too. I never do a whole day of anything...after lunch I rest. I used to keep going for whole days, like three in a row...then I'd have a huge crash that lasted for several days...or longer.
No matter how much we try to deny our illness, it always makes us pay if we ignore it. In a tough situation...like moving or repairing a plumbing disaster...I can keep going with will power. But I make a lot of mistakes and I pay a very big price later on for pushing myself.