Resources for you to browse further

The following resources are in no particular order. Although, I have tried to create some rough groupings to help you. Bear in mind that some websites may naturally fall under several groups, so I have tried to add them under the most relevant group. You may want to bookmark this page and return here to check out more resources in future. I will also add more resources as I come across them.

This is not a comprehensive list – there are many more people working in the CFS space about whom I do not know. So, if you know of good resources, please share them with me so that I can add them here. Thank you.

---

Practitioners and Clinics

The Optimum Health Clinic – treats patients with CFS/ME. The clinic offers a free 15-minute chat to assess whether their treatments could be helpful. Treatments cover nutrition and psychology modalities that have successfully helped thousands of patients improve their condition. Find more details at their website: https://www.theoptimumhealthclinic.com/

Ari Whitten is a leading energy specialist and offers online courses and information on his website: https://theenergyblueprint.com/

Dr Sarah Myhill is an NHS-trained doctor who now runs her own private practice, specialising in the treatment of CFS/ME. She has an amazing wealth of information on her website: https://www.drmyhill.co.uk/

Dr Eva Detko healed her own CFS/ME and now helps others to heal. Her website is: https://www.dr-eva.com/

---

General Information about CFS

Phoenix Rising is a large community-based website that brings together articles about CFS/ME, latest developments in research, and the opportunity for patients to interact and find help and support. You can find the website at this link: https://phoenixrising.me/

---

Charities

The ME Association is a charity set up to inform doctors and patients, and also carry out work to raise awareness of the illness. Their main website is: https://meassociation.org.uk/

ME Action is another body set up to inform, raise awareness and campaign for more research into CFS/ME.  Find their main organisation’s website here: https://www.meaction.net/

They also have a Wikipedia-style site that is designed to inform and educate, so if you would like to research more into the illness, you can find that here: https://me-pedia.org/wiki/Welcome_to_MEpedia

Action for ME is a UK-based charity supporting the needs of patients and their families. You can find their website at this link: https://www.actionforme.org.uk/

---

Research Studies and Organisations

The Open Medicine Foundation (OMF) is both a charity and a research body. It co-ordinates research studies into CFS/ME taking place throughout the world, and also aims to educate and share the latest research findings. You can find the website at this link: https://www.omf.ngo/

DecodeME is the world’s largest study into the genetic causes of CFS/ME. You can follow the results of their research and get involved at this link: https://www.decodeme.org.uk/

---

Free Online Conferences

Keep checking back here to see what online conferences are upcoming. These are great resources for learning about the newest innovations in the field, and finding practitioners who may be able to help you.

Typically, these online conferences will be free to view for a limited time. You can purchase them if you wish to view at your leisure. And if you want to stay updated with what is happening, click here to join my mailing list.

The Mitochondrial Energy Summit: Free summit that brings together over 50 of the world’s leading experts on Mitochondria and energy. Runs from 20th-26th June 2023. Follow this link to find out more or reserve your spot: https://drtalks.com/mitochondrial-summit/

The Psycho-Energetic Root Causes of Illness: Free masterclass hosted by Dr Eva Detko, runs from 26th June until 2nd July 2023. Follow this link to find out more or sign up: https://chronicillnessmasterclass.byhealthmeans.com/