Help for people with ME/CFS in and around Stockport
Stockport ME Group Information Line
0345 519 4116
This is a 24 hour voicemail service. A volunteer will respond to messages left within the next 2 working days. Please be aware that this is a voicemail service only, and that while volunteers regularly check for messages, no volunteer is able to answer a telephone call there and then. Please do leave a message and include your phone number.
The Stockport ME Group have recently changed the phone number. This should be included in your phone provider's contracted minutes and will not be an expensive phone call.
This is an information line number only. Volunteers responsible for dealing with queries will not be permitted to give advice. For Stockport ME Group members, if you have a specific query, numbers on page 2 of HERMES still apply.
Alternatively please email us at email@example.com with inquiries about membership, meetings and other requests for information. If you prefer a phone call please include within your email your phone number and the best time to reach you.
We are currently exploring the option of changing our phone number to an 0345 number which would be included within your monthly landline or mobile minutes.
Views in and around Stockport
Thanks to Stockport MBC for the images.
The Solidarity Drop-
The Solidarity Drop-
They offer support with completion of applications for Personal Independence Payment and Employment and Support Allowance and information on social security sanctions. They can also help with referrals to the appropriate service in cases where advice, or representation in appeals is required.
High Street is on the route of the free Stockport Metroshuttle bus, service 300.
Anyone who is interested in volunteering to work with Solidarity Drop-
Stockport CFS/ME Service
Information regarding Stockport CSF/ME service can be found here
Stockport ME group is on Facebook!
If you are on Facebook come and join the conversation.
Find us on:
or just search for Stockport ME Group.
You will be able to ask questions and chat with other members of the group.
Hope to see you there!
We have registered Stockport M.E. Group with Amazon Smile and this means if people use Amazon Smile instead of normal Amazon and select us as their charity of choice we get a little money for free whenever you buy stuff on Amazon.
It is pretty easy to register. If you have never used Amazon Smile then you will probably do most of it by clicking this link and then maybe ticking YES and then just remembering to use Amazon Smile rather than Amazon or download the Amazon Smile app and use that instead of the more or less identical Amazon one.
The more people who do this the better whether they are SMEG members, friends, family
etc. Everything we raise does get re-
If you are already with Smile it is really easy to change your charity to Stockport ME Group. The slightly tricky thing is we wont come up in a search for "Stockport ME Group" either remove the ME or add "M.E." with the full stops and your sorted. Again you can click on the above link to do this.
Friday 11th June
Awareness & Embodiment Practices for Nervous System Health – Amy Davies
Amy will talk about the importance of nervous system health when experiencing fatigue
conditions such as ME and CFS. She will share insight into how we can improve the
health and regulation of our nervous system through awareness and embodiment-
Amy is a Yoga Teacher, Coach and Mindfulness Meditation facilitator who specialises in supporting individuals experiencing persistent pain and fatigue, alongside those looking to reduce stress and build resilience. Her approach is heavily influenced by somatic movement.
This is a gentle practice that encourages us to focus on how the movement feels, rather than how it looks. Expect friendly and accessible sessions, when working with her. Amy’s approach is practical and informative; she shares both the ‘why’ and the ‘how’. Her aim is to offer tools and techniques to support others in their everyday life. You can find out more over at: https://amydaviesyoga.co.uk/about/
or follow her on Instagram https://www.instagram.com/amydaviesyoga
Friday 9th July
Justine Jackson on aromatherapy for ME/CFS
Justine Jackson is an expert in the field of aromatherapy. She qualified in 2006
and has worked as a clinical aromatherapist for 15 years within a multi-
Justine will talk about aromatherapy and supporting you during your journey through
ME. She will discuss how ‘hands on’ treatments need to be tailored to the individual
and how clinical aromatherapists blend the essential oils they use and don’t use
preblended oils. Aromatherapists will see how your body responds and will design
treatments which are very gentle and encourage the body to heal itself. Justine will
explain how aromatherapy isn’t just about the hands-
As with all the SMEG meetings this is open to everyone (not just SMEG members) so please do join us if you can, it would be lovely to see you. Details for joining the meeting are below. If there is anyone who would like to join us but is not that familiar with Zoom please do get in touch with one of us on the committee and we will do our best to help. Also, do feel free to join just for a short while and say hello. You can also join and not have your picture seen (we can still hear your voice and you can see and hear us) or you can call from your phone if you do not have a computer.
You will be able to login after about 10.30am if you would like to join us for a chat before the actual meeting starts at 11am.
Join Zoom Meeting
Meeting ID: 777 116 5459
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Meeting ID: 777 116 5459
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Group Specialist ME/CFS sessions online via Zoom with a specialist ME/CFS Nurse
We are aiming to run, subject to demand, 6-
We have long been concerned that about half of Greater Manchester and the surrounding areas do not have access to any specialist services. Even where services do exist there are issues such as year plus waiting lists or the services are not accessible to people who have real difficulty getting out of their house. These sessions are being funded by Stockport ME Group and will be primarily targeted at people who have been diagnosed with ME/CFS but have been given no specialist treatment.
If you or anyone you know might be interested, then please get in touch with Ben Wickens ideally by email at
Due to timings, this is likely to start before the next HERMES newsletter comes out so it will be hard to inform our whole membership. If you do know anyone who this might be suitable for who is not on Facebook, our email list or who does not regularly check our website then please reach out to them. We have not sorted out an exact start date or time for the sessions as this will depend in part on the availability of those interested in attending but, we are looking for it to start sometime between July and September.