Discuss this article on the forums
The Forums are a major part of Phoenix Rising. In recognition of this we have allotted a permanent space on the Phoenix Rising Board of Directors to be filled by a Forum member. Depending on how many nominations come in we will hold a vote; and the top three nominees will go to the Board and one person will be chosen.
The Forum Board Members main job will be to guide and assist Phoenix Rising in its core mission – to enhance the health of people with ME/CFS. A secondary objective will be to provide feedback back and forth from the Forums to the Board and vice versa when appropriate. The Board meets via teleconference calls at least four times a year, receives monthly reports on PR, and is engaged on variety of issues.
No specific hours are required although we are looking for someone who’s energetic and healthy enough to participate on an ongoing basis. The Forum Board member does not have to have CFS, caregivers or supporters are welcome as well. Specific skills are not required but we will keep an eye open to fill some of PR’s skill needs as well.
You can nominate someone else or yourself. If you’re interested or think you might be interested please contact us at firstname.lastname@example.org
Current Board Members
Mark Berry – BSc Mathematics (University of Manchester), MSc Computer Science (University of Birmingham).
Mark has had ME/CFS – diagnosed as “Multiple Chemical Sensitivity” and an “ideopathic immune disorder” – for 15 years. He has managed to work part-time from home as a software engineer for most of that time, and currently works as a Portal/Web Developer at the University of Nottingham.
Mark is a moderator on the Phoenix Rising forums, and is excited about the potential of the software projects he’s developing with Phoenix Rising to enable ME/CFS patients – as well as their organisations, charities, advocates, supporters, physicians and researchers – to meet, share, collaborate, communicate, document their illness and experience, and campaign and work together for a better understanding of ME/CFS, fair treatment by medical and statutory authorities, and a huge increase in the derisory levels of biomedical research funding for ME/CFS and other severe and idiopathic neuroimmune diseases.
Adin Burroughs (Board Member) – Adin graduated from University of Central Florida in 1993. From 1994 to 2000 he was Chief Surveillance Mission, Weapons Air Director, Chief, Plans And Exercises, Chief and Operations Crew in the USAF. From 2000 to 2002, as a Senior Systems Engineer for Scientific Research Corporation, Adin provided technical engineering support to the USAF’s Theatre Air Command and Control Simulations Facility. As a Program Manager for Northrop Grumman from 2002-2005 he lead soft/hardware teams in datalink/command and control markets. Adin first became ill with chronic fatigue syndrome in Judy, 2003 and stopped working in Oct. 2003. He is currently disabled.
Cort Johnson (President/Board Member)- a BA in philosophy (LBSU) and a Masters in Environmental Sciences (SJSU). He has had chronic fatigue syndrome for over 30 years. He created the Phoenix Rising website in 2002, the Phoenix Rising Newsletter in 2005 and the ‘Bringing the Heat’ blog in 2009. The Phoenix Rising website – one of the most information rich ME/CFS website – contains hundreds of pages of articles on chronic fatigue syndrome research, treatment and other issues. In 2009 he created the Phoenix Rising Forums which quickly became the most popular communication interface for people with CFS on the internet. He regularly attends and testifies before Federal Advisory Committee meetings on CFS and conferences on the subject. You can find his story here (https://aboutmecfs.org/Story/Cortsstory.aspx )