Posts - Myalgic Encephalomyelitis Community | HealthUnlocked

Myalgic Encephalomyelitis Community

2,136 members•660 posts

All posts for September 2018

The Gupta Programme

Does anyone have any experience of doing this programme by Ashok Gupta about retraining the Amygdala (part of our brain that is responsible for the “fight or...

Does anyone have any experience of doing this programme by Ashok Gupta about ret...

amasufindme

•7 years ago

15 Replies

Uk GPs only now informed of WHO classification 1995

As of 1/8/18 UK goverment recognises M.E/CFS as neurological as per WHO 1995 Maybe now we can get all the help we need and not be treated inhunely

As of 1/8/18 UK goverment recognises M.E/CFS as neurological as per WHO 1995 May...

Charlie1606

•7 years ago

2 Replies

Scared.

Every time I have a crash which usually lasts for two months, all I can think of as I lie down on the bed useless to myself and anyone else is to kill myself....

Every time I have a crash which usually lasts for two months, all I can think of...

jo19

•7 years ago

6 Replies

Want to take advantage of all our features? Just log in!

They said it didn't exist!!

I was diagnosed with CFS/ME along side fibromyalgia a year ago. Exhausted all the time which I thought was a symptom of my heart failure afew years ago but...

I was diagnosed with CFS/ME along side fibromyalgia a year ago. Exhausted all th...

BeeBee50

•7 years ago

1 Reply

I have Cfs/m.e and pots but am going through investigations for a 3rd time due to having vertigo etc the past 6months. Any Tips on coping?

Very worried it’s untreatable. It took the Doctors years and years to find out I had pots in the past so suffered years of dizziness

Very worried it’s untreatable. It took the Doctors years and years to find out I...

Ponymad

•7 years ago

16 Replies

Pots weird blood test ?

Hey i was just wondering if any one could help me i have dysautomia pots plus me/cfs plus histimine intolerance and far few other things that my tierd finger...

Hey i was just wondering if any one could help me i have dysautomia pots plus me...

H2090

•7 years ago

1 Reply

Search posts

Pinned Posts

See all

Community Guidelines

Want to be a Community Ambassador for Myalgic Encephalomyeli...

Latest poll

See all polls

If ever been seen by UK 'CFS/ME' clinics what was your experience? Tick any that apply. (Will be more polls on this subject in future too!)

Vote

Topics

All posts(170)

Anything re ME & CFS(101)

Research(13)

General chat(10)

Newcomers (10)

Questions, Answers(9)

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.

Posts - Myalgic Encephalomyelitis Community | HealthUnlocked

Myalgic Encephalomyelitis Community

All posts for September 2018

The Gupta Programme

Uk GPs only now informed of WHO classification 1995

Scared.

They said it didn't exist!!

I have Cfs/m.e and pots but am going through investigations for a 3rd time due to having vertigo etc the past 6months. Any Tips on coping?

Pots weird blood test ?

Search posts

Pinned Posts

Latest poll

If ever been seen by UK 'CFS/ME' clinics what was your experience? Tick any that apply. (Will be more polls on this subject in future too!)

Topics

Archive