Open Medicine Foundation®
Leading research. Delivering hope.
ME/CFS and related chronic complex diseases

Worldwide Tour Blog


Dream. Believe. Do It . . . Join Team OMF in Hope

RME Sweden Shares Blog Post on Worldwide Tour Visit

(Blog Post translated by Google Translate and shared with permission from the RME website.) Member meeting in Borås, part 1-Visit by Linda Tannenbaum from Open Medicine Foundation Camilla Gillberg, RME Sweden’s Secretary, reports from Member meeting held in Boras on Sunday, and also tells us when she met Linda Tannenbaum for the first time: For 3.5 years ago, in October...

Read More

Reunited with My Swedish Friends (OMF Sweden): June 17-20

Traveling is an adventure. Yesterday after a flight and two trains, I arrived in Gothenburg 11 1/2 hours after I left my hotel in Bergen, Norway. I certainly saw some beautiful sights along the way (picture: view from the train)! Erik and Lena Nilsson kindly made all the arrangements for my visit. They picked me...

Read More

The Strength of Support Groups – Reflections from the Tour

On my travels through Europe I am reminded of the incredible work done by national organizations and local support groups on so many levels, and how important these groups are for patients and parents in those countries. Most European countries have one or several big and smaller support groups, with members ranging from a few...

Read More

Visiting Norway, Home to Two of Our Newest Scientific Advisory Board Members (June 12)

I am in my fourth week of OMF’s European Tour of Hope and had the joy today of being able to meet with our Norwegian ME/CFS friends again. They welcomed me warmly in beautiful Oslo, a city surrounded by the most spectacular scenery, including fjords, lakes, mountains and forests. The Norwegian ME Association organized a...

Read More

Day 14: Antwerp – Belgium (June 7)

Nederlands Today, for the first time, I visited Belgium. What a beautiful country with wonderful medieval towns. My husband Don accompanied me to a conference hosted by Wake Up Call Beweging. 55 people, mostly patients and parents, attended the event. Some of these parents have very young children. Their personal stories touch me deeply, and...

Read More

IiME Conference: Patient Day (June 2)

I have been attending the IiME Conference for four years. Each year, one of the highlights of the conference is the Patient Day. This is the day when new and old friends come together and feel the support and strength of our community. Each year I am inspired by the commitment and resolve of the...

Read More

Inspiring visit from Linda Tannenbaum, from OMF in California, 24 – 26 May

Information provided by Celia Marshall, ME Support, Isle of Man We gave Linda a jammed packed programme of meetings with various people including the Minister Kate Beecroft (photo), presentations to Members of Tynwald (Isle of Man Parliament) a public meeting, informal meetings with members, and Manx Radio, all to raise awareness and move forward government plans to set...

Read More

Tour Impressions: “My heroes are not footballers or movie stars, but people like you and Ron”

It has been so heartwarming that everywhere I visit in Europe, people are so happy and appreciative to hear first-hand research updates. They are feeling a sense of real hope for a better future. One of the Isle of Man organizers contacted OMF saying, “My heroes are not footballers or movie stars but people like...

Read More

Major announcement from Northern Ireland following OMF visit

Dear Friends, I have a very exciting breakthrough to share with you as a result of our tour of hope and visit to Northern Ireland Dr. Ian Clements, Chairperson of the Health and Social Care Board has confirmed that ALL 365 General Practitioner (GP) practices in Northern Ireland will receive new updated information on ME/CFS...

Read More

Linda’s Impressions: “My heroes are the fighting patients and parents I have met so far”

I am one week into my European tour of Hope. I have been to the Isle of Man, Ireland and Northern Ireland. This truly has been a fantastic experience meeting passionate advocates, caring people, desperate parents, and wonderful, determined patients. With so many people showing up to the talks in these countries, I can’t possibly...

Read More

Stay Informed

Be the first to hear our research news.

Subscribe Now.

No thanks