Happy International Wheelchair Day
Happy International Wheelchair Day!
Today, we celebrate the incredible resilience, strength, and freedom that wheelchairs bring to millions around the world.
Happy International Wheelchair Day!
Today, we celebrate the incredible resilience, strength, and freedom that wheelchairs bring to millions around the world.
Myalgic Encephalomyelitis – Ear Seeds Myalgic Encephalomyelitis, Ear Seeds, Dragons Den
Christmas with Myalgic Encephalomyelitis is hard so if you are suffering this Christmas I send you all my love.
You are not alone, I just wanted to let you know that if you have Myalgic Encephalomyelitis and need a friend or just someone to talk to over the Christmas holidays, please feel free to message me. I’m not claiming to have all the answers or to be able to solve your problems, but I am a sufferer too.
A Cuddly Labrador, A Sneezy Labrador and a Funny Labrador it must be Vlogmas Days 14 & 15.
📆 This video was published on or around 17th December 2023
Welcome to my enchanting world, where the holiday spirit dances in each frame, somedays🎅✨
Vlogmas Day 8 : Unboxing Pooch & Mutt Treats & Advent Calendar Time
Alfie has his favourite treat box delivered The Pooch & Mutt Treat box 🐾
Watch Alfie Our Black Labrador open Day 8 of his Lilys Kitchen Advent Calendar🐾
Vlogmas Day 2: The Blush & Gold Planner Unboxing & Alfie opens up his Lilys Kitchen Advent Calendar door number 2 🐾
Watching Alfie opening day 2 of his advent makes me so happy, he deserves the world🐾
Could Tea help your pain symptoms ? Could tea help your
Facebook Twitter Youtube Instagram Tiktok Pinterest Myalgic Encephalomyelitis/CFS Symptoms and What
I think it is only right for me to share with you my must-read book recommendations for Myalgic Encephalomyelitis sufferers. I have turned to these books many times since my diagnosis as it is incredibly scary to start feeling worse with an illness like Myalgic Encephalomyelitis. So any time that I started getting more pain or I felt worse than normal I have used these books to see if it could be additional Myalgic Encephalomyelitis symptoms.
The Government has written a plan to improve the lives of people living with Myalgic Encephalomyelitis but is it too little too late? When I was first diagnosed with Myalgic Encephalomyelitis in 2012 I was relatively lucky, now ok The appointment to see the ME Team in Liverpool was lost and then budget cuts happened so I didn’t see someone as soon as I needed to
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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