This will kill me.
I have to hold my hands up and say that recently
I have to hold my hands up and say that recently
This may sound naive but surely Black Lives Matter applies to Black people the world over.
I hate borders and how the location in which you were born dictates most lives.
An Hour for Others is a local charity here in Liverpool. For my Birthday I want people to donate to them instead of buy me cards or gifts.
Have you tried the coffee that is all over social media
Amazon buys #2 is the second review post reviewing items that could help people with ME.
It’s not long now till our ME Pyjama Party and all
Reviewing Amazon products from the point of view of someone with a disability, welcome to my new series Amazon Buys #1.
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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