Tag Archives: symptoms

What is ME/CFS?

ME/CFS (Myalgia Encephalomyelitis/Chronic Fatigue Syndrome) is a chronic debilitating illness characterised by fatigue that does not go away with rest. The newest name for the illness is SEID (Systemic Exertion Intolerance Disease).

There are many symptoms including:

  • Fatigue not eased on resting
  • Flu-like symptoms
  • Brain fog
  • Poor concentration
  • Dizziness
  • Low blood pressure
  • Palpitations
  • Sensitivity to light and sound
  • Headaches
  • Fatigue on exertion
  • Muscle weakness
  • Muscle spasms and twitches
  • Abdominal pain
  • Bloating
  • Constipation
  • Food intolerances
  • Insomnia
  • Adrenal fatigue
  • Anxiety
  • Post-traumatic stress disorder (PTSD)

With Fibromyalgia there are additional symptoms of:

  • Systemic pain

CFS is diagnosed by elimination after various NHS tests such as blood tests, endoscopy, ECG, postural tests, MRI scan etc. If all their test results come back negative then they may diagnose you with CFS.

Often people with ME/CFS are housebound or even bedbound. The illness can last for a few months to several years. I had CFS for 3 years and after making diet and lifestyle changes was able to function in society again.

I hope this information has helped you to better understand ME/CFS/SEID.

ME Question & Answer Session 2

I have had more questions from ME sufferers, so I have decided to create a second ME Question & Answer Session post, as the answers may be helpful for other people with ME who read my blog.

Q: Are ME and Chronic Fatigue Syndrome the same?

ME stands for Myalgic Encephalomyelitis.  Mya = muscle, algic = pain, encephalo = brain, myelos = marrow, itis = inflammation. So overall ME means muscle pain and inflammation of the brain and spinal cord.

Chronic Fatigue Syndrome (CFS) is a group of symptoms including fatigue which after months of testing have no other diagnosis. I was diagnosed with Chronic Fatigue Syndrome after a year of tests. I did not have muscle pain, which can also be diagnosed as Fibromyalgia, nor did I have inflammation of the brain and spinal cord which were checked after a CT scan.

However the terms can be used interchangeably.

Q: How bad were your symptoms at your worst?

At my worst I had severe fatigue, brain fog, poor concentration, dizziness, muscle weakness, sudden collapsing, sensitivity to light and sound, extreme fatigue on light exertion and insomnia.

Q: Other than a vegan diet have you found any other useful changes that have helped you improve?

Yes having a more relaxed lifestyle. Working part-time so I have time to meditate, do yoga and be creative. I have learned that people with ME/CFS often hyperventilate and are stressed out easily. They need to learn to slow down and slow their breathing down. Buteyko breathing is helpful. Counselling is also helpful and they may have an unresolved emotional trauma from the past which is draining their energy and needs to be faced and released.

Q: Do you take any supplements of any sorts or any other form of medication?

I take a liquid multi vitamin and digestive enzymes. I also take a probiotic supplement to support the good bacteria in the gut. I don’t take any medication.

If you have any questions about ME/CFS please do not hesitate to contact me as I will be happy to help!