Welcome to YouTube
Welcome to my YouTube channel my name is Alisha
Welcome to my YouTube channel my name is Alisha
Do you qualify for free Rapid Lateral Flow Tests from GOV ?
Could Ketamine be the answer Myalgic Encephalomyelitis sufferers are looking for?
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
Where do you go Online Lingerie Shopping? Where do you go shopping for underwear when you are unable to make it into a shop? For me, it has to be Next or Marks and Spencer. Not only do you know the quality is going to be there if you are unhappy you can send it back without an issue.
Living with a chronic illness is extremely difficult but what is it really like on a good day or on a bad day?
Being bedridden, I spend almost all day in Pyjamas, so when I needed a little retail therapy, I thought it would be silly not to film the unboxing and put the Pyjama Haul up on Youtube.
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
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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