Last 10 active topics

Did anyone try Dr Cheney protocol with artesunate (hepasunate from hepalin.com is the one used) and woorwood elixir?

Supposed to have good antiviral properties and help diastolic dysfunction food in cfs, only downside is potential liver toxicity

It's now a building block of his protocol

It's 50$ US for 3 months which isn't bad

Thx!

Anyone kows were ntf is available? i read about it here http://rockycha.wordpress.com/ but i couldn't find a contact for the girl who writes this blog

anyone heard of Jumpstart? It's an herbal stimulant, Haven't tried it bt am thinking about it.

I started taking Gene-Eden (antiviral natural supplement) when my daughter got the Mono, she recovered faster, and when I got the disease few weeks later, I hardly felt it because the symptoms were so weak...

Ever since it mainly helped me dealing with my sleep disorder, and energy level that were really low.
now I am hardly waking up at nights, my sleep is deeper, and my energy level is increasing constantly.
I started with ...

I have cfids and find 2 things that make my life a little more tolerable.Whey protein from Immunotec canada which has helped erase my chronic sore throat. It ,more importantly, has helped with the debilitating fatigue. It is whey protein which is available everywhere at a fairly low cost. I am told it is inefficient for people such as us .So b/c of desperation I pay 200 /month. It works tho'. I try to ...

Can anyone recommend a site for purchasing supplements online in bulk to save money? I usually buy from my local health food store but I know they mark up their products a lot.

I will be continously updating and editing this post, so bear with me. There's alot of supplements here folks. It seems that not everyone's CFS/Fibro is the same, and each supplement will not have the same effect on you that effects me. Translation: Do not take my word as gospel! I have spent nearly $2,000 on supplements and a decent percentage of that has been wasteful. I'll try to eventually list all my symptoms and ...

Hi,

I'm interested in trying vitamin b12 but every doctor I have mentioned it to has refused to have anything to do with it. Does anyone know of any UK doctors who are willing to use it? Someone in Berkshire/Oxfordshire/Buckinghamshire/London would be ideal.

Thanks,

Emma

I take digestive enzymes. By default, I found that if I eat a high protein meal and take enzymes I don't get cloudy urine. My own doc didn't even know what to make of it. I'm guessing I don't have enough natural enzymes of my own to break down protein.

I'm wondering if I should also take them on an empty stomach to try to heal the lining of the gut. They are so expensive ...

Hello ,this is my first post..... :)
I have cfs and I 'm now trying to take a vitamin b complex with 50 mgs of each vitamin(excluding b12 that is 50 mcg)
but, for now, I'm getting worse,
someone has had this experience?
is it normal?