The ME/Chronic Fatigue Syndrome Service has arranged an opportunity for young people aged 16 to 25 who have a diagnosis of ME/Chronic Fatigue Syndrome (CFS) to meet other young people and share experiences.

There will be refreshments, resources and information, plus clinicians available on the day.

Those aged under 18 must be accompanied by a responsible adult.

The peer support group will take place on Wednesday, 4 March, between 3.30 and 5.00pm at Community Roots, Deepdale Stadium (by Minerva Health Centre), Lowthorpe Rd, Preston PR1 6SB.

It would be helpful to understand how many people are attending, and we encourage you to register for the event on the Community Roots website; however, no one will be turned away on the day. To register, you will need to create an account.

What is ME/CFS?

Myalgic Encephalomyelitis (ME), Post Viral Fatigue Syndrome (PVFS), and Chronic Fatigue Syndrome (CFS) are some of the names used to describe a syndrome, whose main feature is excessive fatigue.

ME/CFS is the preferred term used in this information. It more accurately describes the illness and is now officially recognised. ME/CFS affects people in different ways, and no two people experience the illness in the same way. The main feature is persistent physical and mental fatigue, which differs from normal tiredness. It is not adequately relieved by rest and is usually out of proportion to the activity undertaken.

A range of other symptoms often accompany the fatigue. These include muscle and/or joint pain, headaches, swollen glands and recurring infections often sore throats. Some people have feelings of dizziness and temperature fluctuations. There are frequently some difficulties with memory and concentration, and many people experience problems with their sleep. They often have vivid dreams and wake feeling unrefreshed. Many people describe sensitivity to some foods and medicines.

Currently, there is no specific diagnostic test for ME/CFS. However, there is a clear protocol and criteria that are used to confirm the diagnosis. A diagnosis is made by excluding other conditions that cause fatigue.

The ME/CFS Service aims to provide supportive, holistic patient-centred advice to aid acceptance, education and self-management for adults with mild or moderate ME/CFS.

 You can find out more about the ME/CFS Service.