Absolutely Heartbroken
Please help me raise enough money to buy a wheelchair accessible vehicle
Please help me raise enough money to buy a wheelchair accessible vehicle
Painful Periods with Heavy Flow and sharing a little too much
This winter is going to be very hard for lots of us so here is my suggestion to help reduce the pain levels down for sufferers of chronic pain.
Could you live a life in severe pain, pain so severe you can’t think straight
If you have a loved one or friend who has an underlying health condition please check on them over the next few days
In Liverpool football means everything, our families are born to be
I don’t normally celebrate my Birthday but this year is going to be differerent
Today is Tuesday 3rd May 2022 and the time is 04:30,
Friends with ME is a new community set up by ME Sufferers for ME Sufferers.
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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