The ME Pyjama Party
I’m thrilled to invite you to a special event that aims to make a significant impact in the lives of those living with Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS).
I’m thrilled to invite you to a special event that aims to make a significant impact in the lives of those living with Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS).
We are all ready in Our Red PJs to help raise awareness of Myalgic Encephalomyelitis.
To join us all you need to do is take a pic in your PJs and post it to social media using #MEPJParty
ME/CFS is a complex, multifaceted disorder that affects various body systems, including neurological, immune, endocrine, and energy metabolism.
Facebook Instagram Twitter Youtube Pinterest Myalgic Encephalomyelitis is not just tiredness.
As a passionate advocate for Myalgic Encephalomyelitis (ME) a complex and debilitating condition, I am deeply committed to raising awareness about the complexities and overwhelming impact of this condition.
According to the NHS Website, Chronic fatigue syndrome (CFS) is a long-term illness with a wide range of symptoms. The most common symptom is extreme tiredness
For more information please visit https://www.nhs.uk/conditions/chronic-fatigue-syndrome-cfs/
People with ME/CFS have fatigue that is very different from just being tired. The fatigue of ME/CFS:
Worsening of ME/CFS symptoms after physical or mental activity that would not have caused a problem before illness. This is known as post-exertional malaise (PEM).
Sleep problems.
Many but not all people with ME/CFS have other symptoms.
Pain is very common in people with ME/CFS. The type of pain, where it occurs, and how bad it is varies a lot. The pain people with ME/CFS feel is not caused by an injury. The most common types of pain in ME/CFS are:
Some people with ME/CFS may also have:
Myalgic Encephalomyelitis does not have a cure.
Find a Dr or Consultant who listens to you is the first step
It is a manageable condition and depending on the severity of your symptoms the more difficult this can become.
I advise learning to listen to your body and what it is telling you. If you feel tired rest and if you feel pain find a solution to reduce that pain, this could be through pain medication prescribed by your Dr.
I am not saying that finding a Dr who listens or listening to your body is going to be easy as this illness is incredibly complex for some and manageable for others.
Having a Dr who listens to you or reads about the latest drug that sufferers are recommending can take a lot of unnecessary stress and anxiety from the sufferer.
It would be best for me to point you to the above question What is Myalgic Encephalomyelitis?
Most pages list the illness as ME/CFS or Myalgic Encephalomyelitis/Chronic Fatigue Syndrome or sometimes even Systemic exertion intolerance disease (SEID).
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