Reclaiming my Independence
Help make a real difference to my life by donating to my Gofundme page, your donation will help me purchase a larger car, Progeo wheelchair and Mototronik
Help make a real difference to my life by donating to my Gofundme page, your donation will help me purchase a larger car, Progeo wheelchair and Mototronik
From my toilet I share how life with Myalgic Encephalomyelitis really makes me feel and why it is so hard to win against ME
Today I read about someone like me choosing to end their
This is something the I rarely discuss and I can’t believe
I aim to create a community that embraces diversity, fosters understanding, and supports one another on our good and bad days on this beautiful journey we call life.
Yesterday I had an appointment with my doctor to discuss the pain and loss of movement in my hands
Recently I filmed a What’s in my bag? video for Youtube,
Alfie tries Lilys Kitchen dog treats. Alfie tries Lilys Kitchen dog
COVID-19 and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) mirror the same effects
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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