Last 10 active topics

Hi All,

I am currently working on a project to gather the stories of people who have recovered from moderate/severe, classic ME/CFS.

Unfortunately, there aren’t many people who have recovered from this illness. It thus seems important that we learn from the few who have recovered.

I’ve spent the past three years gradually regaining my own health. Now that I’m close to being really well, people ask me a lot of questions about my experience. ...

OK I am in Australia but am willing to travel i dont care where but def uk would be the easiest as i have family there.

I am willing to try most things but like to research before I go ahead, I have been reading this board and there is all sorts of GBA, CFA, ATX etc cant rem all the acronyms and have no idea what all the acronyms even mean. But when you ...

hello everyone!

on the EFT forum I have been advise to do some exercises to correct the body energy flow.

Here are some explanations;

CFS is not a disease.
It's an energy condition.
That energy condition of "homolateral" can be easily normalized with a "homolateral repatterning drill".
That drill takes about 3-5 minutes to do.
Since you've had it long term you probably need to do that drill 4-5 times a day.
That specific drill ...

it sucks being 25 and having cfs. Trying to keep up with the social life is so difficult. I feel terrible today i regret it everytime. I hate this i'm so strict through the week then the weekend messes it up. If i had a girlfriend i would probably stay in but being single i hate stayin in at the weekend its too lonely.

Hello, I'm new to these forums, and have a few questions that I'd Like to ask :)

I'm going to be 17 in a few weeks. About 16 months ago, I was diagnosed with CFS after having glandular fever. I missed a year of school (UK year 10) but still managed to pass all my GCSE's that I took in the summer of this year.

Now what ...

I found this on You tube that really explains brain wave patterns. It seems that if most CFS are in fight or flight, we are in Beta mode. We need to strive for an Alpha state. It is a good explanation.
http://www.youtube.com/watch?v=v2UJrfXu ... re=related Part 1
http://www.youtube.com/watch?v=pSJyJzR8 ... re=related Part 2

I live in the uk and i've been on employment and support allowence for good part of 9 months now at the reduced rate because i'm still on appeal for it.

I'm going to university part time starting in a couple of weeks this is only 3 hours weekly of classes. Would I still be entitled to the benefits? anyone in a similar situation or had experience of this?

Thanks
Neil.

Hi everyone, I'm new to this forum - wish I had found it years ago!

Since I am new here, I thought that I would write a bit on my adventures with this wonderful illness... perhaps my experiences can be of assistance to someone else... and if not, well this is the first time that I have found a place where it seems people actually understand what I've been going through.

It all started about ...

I was diagnosed with this in addition to my cfs. I believe that this is the sinuses in the cheek bones. I had a x-ray to confirm diganosis and it showed both of them were blocked. I don't know if theres any treatement. The doctor did tell me that this could be the cause of my headache and the tightness in my face.

Anyone on here had experience of being diagnosed with maxillary sinusitis. If ...

http://www.cfscentral.com/2010/08/fdani ... thing.html

They found (i think) 8 different types of mutated XMRV. So that might have been why they had problems detecting them in the other studies.