ME / CFS is a Real Disability! Questions? Ask Here!

What is ME and CFS?

Myalgic Encephalomyelitis (ME) is also known as Chronic Fatigue Syndrome. This is a long-term illness with a wide range of symptoms. The most common symptom is extreme tiredness.

My Story - Me and ME

I am Joy. I am a listener here on 7cups and i am not without my own struggles, i have many health issues mental and physical and i live with ME/CFS. There are good days - there are pretty damn bad days where i am completely bed ridden. I have chosen this time to tell you of my health because I believe the awareness of this illness is important.

You Can Ask Anything!

If anyone has any questions please ask away - I can't speak for anyone else's experience but i can explain mine. Whether you are a sufferer yourself, or you have a family member or friend that you are unsure how to support or just want to know a lil more. Please ask - No question is wrong - No judgement here!

Below are a few bullet points about ME and CFS…

- There is not a specific test for CFS/ME, so it's diagnosed based on your symptoms and by ruling out other conditions that could be causing your symptoms.

- Treatment for CFS/ME aims to relieve the symptoms.Most people with CFS get better over time, although some people do not make a full recovery. It's also likely there will be periods when your symptoms get better or worse.

- Living with CFS/ME can be difficult. Extreme tiredness and other physical symptoms can make it hard to carry out everyday activities. You may have to make some major lifestyle changes.

- CFS/ME can also affect your mental and emotional health, and have a negative effect on your self-esteem.

Below is a summary image of a few of many symptoms people experience with ME/CFS…

https://www.meaction.net/ - Action for M.E. tackles ignorance, injustice and neglect for people whose lives have been stolen by M.E.

Remember.... Please ask anything you wish - No question is wrong - No judgement here!

Stay Strong and Keep Fighting!

- Joy <3