Severe ME Day of Understanding and Remembrance: Aug. 8, 2017
Determined to paper the Internet with articles about ME, Jody Smith brings some additional focus to Severe Myalgic Encephalomyelitis Day of Understanding and Remembrance on Aug. 8, 2017 ...
Discuss the article on the Forums.

OMF Newsletter June 2017

Discussion in 'Latest ME/CFS Research' started by Ben H, Jun 15, 2017.

  1. Ben H

    Ben H OMF Correspondent

    Messages:
    771
    Likes:
    8,588
    U.K.
    Hi guys,

    Latest Newsletter for you-lots going on!

    [​IMG]

    June 2017


    Community Symposium on the Molecular Basis of ME/CFS
    Sponsored by OMF
    Saturday, August 12, 2017 at Stanford University

    Come hear from our amazing team in person!
    Join us for a unique and unprecedented opportunity to learn from and interact with these world-class scientists.

    Learn more.
    Register here.


    Major Patient Care Improvements Coming In Two Countries

    Dream. Believe. Do it. Join Team OMF in HOPE.

    [​IMG]

    The End ME/CFS Worldwide Tour in Europe has been very productive in the first two weeks. The first stop of the tour was in the Isle of Man, where we met the incredible ME/CFS community leaders, Celia Marshall, Phil Gawne and Craig Morris. Our two-day visit included meetings with patients, family members, government officials, and physicians.

    As a result of the Parliament meeting, the Isle of Man government has already agreed to set up additional ME/CFS services for both adults and children. (Photo: Linda Tannenbaum & Kate Beecroft, Minister of Health and Social Security) Read more.

    [​IMG]

    Our visit in Northern Ireland was organized by the Hope for ME & Fibro group under the dedicated leadership of Joan McParland. Since 2011, Hope for ME & Fibro has been bringing together world experts and researchers for their annual conference, which we were honored to take part in this year. Immediately after our visit, there was an announcement of improvement in medical education: all General Practioners in Northern Ireland "will receive new updated information on ME and fibromyalgia, including biomedical research, confirming the very physical nature of the disease." (Photo: conference panel & leadership from Hope 4 ME & Fibro.) Read more.

    These visits underscore the importance of not only seeking a cure for patients worldwide but also of raising awareness in the general public, the media, government and healthcare professionals.
    ME/CFS is truly an international problem. So many patients have their lives on hold. We must continue to fast-track our efforts to find a cure. It is also crucial to improve the education of physicians and advocate for better support services for patients.


    End ME/CFS Worldwide Tour Blog Shares Stories of Courage and Strength

    [​IMG]
    We invite you to follow the European Tour. With almost daily posts, Linda Tannenbaum, CEO/President, is sharing poignant moments and individual stories of courage and strength, all while building a world-wide network of patients, parents and caregivers. Please follow the Tour on Facebook, Twitter, and our website.

    Support Research

    Please donate today to help fund the upcoming Collaborator Meeting and Community Symposium at Stanford.

    Your donation will support OMF's sponsorship of this important research meeting.

    On August 10 and 11, we are bringing together an outstanding team of scientists from all over the world, with whom Dr. Davis has already been collaborating on ME/CFS research. Assembling this diverse expertise in one room will be the ideal opportunity for this team to interpret their collective research results and to set a strategic and collaborative path forward. OMF is underwriting the cost of the two-day scientific meeting and is supporting the Community Symposium on August 12, where you as a patient can meet our scientists in person and be updated firsthand on the latest progress in research and future plans.

    Dr. Davis and Linda Tannenbaum, both parents of sick children, are committed to finding answers and a cure. They are driven to help their children and millions of patients around the world. They know the best way to achieve our goal is by working together in a collaborative and open environment.

    Donate today to make their vision a reality for all patients around the world.


    Open Medicine Foundation
    Tax ID: 26-4712664
    Our Purpose:

    • To fast-track revolutionary research for ME/CFS and related chronic complex diseases.
    • To support collaborative scientific research to discover molecular causes, find effective treatments, diagnostic markers, prevention approaches and cures.
    • To communicate, engage and inform the patient community.
    • To help drive & support global collaboration
    A Word from our CEO/President
    [​IMG]

    OMF's approach to finding answers is broad-based. We recognize that building global collaboration with the patient and scientific community will help to fast-track answers. With that in mind, we launched the End ME/CFS Worldwide Tour. In addition, we are honored that researchers from around the world are traveling to join Ron Davis and team for the upcoming Collaborative Team Meeting and Community Symposium on the Molecular Basis of ME/CFS. These are two examples of how we are working with you to find answers.

    We need your help to go further. I invite you to please support our efforts and donate to help OMF find a cure for patients around the world. Together we are stronger!

    Thank you being our partner in finding answers.
    With shared hope for all,
    [​IMG]
    Linda Tannenbaum
    CEO/President
    Linda@omf.ngo

    Donate Now
    to join the Team of HOPE!
    [​IMG]
    Turn Your Online Shopping
    Into Donations for Research
    [​IMG]
    [​IMG]
    Donate your old car, boat or plane
    and turn it into $$ to support research.
    (Available in the US only)
    [​IMG]

    Create your legacy.
    Please consider including OMF in your will & estate plans. Learn more.
    We invite the patient community to get involved by sharing with friends and family on Social Media.
    [​IMG] [​IMG]
    Like us on Facebook
    Follow us on Twitter
    Please visit our website at
    www.omf.ngo



    If you would like to donate to support OMF's sponsorship of this incredible Symposium, that would be fantastic.

    Thanks guys,

    B


    @Janet Dafoe (Rose49) @AshleyHalcyoneH
     
    ahimsa, Johannawj, Sean and 15 others like this.
  2. jimells

    jimells Senior Member

    Messages:
    2,001
    Likes:
    6,115
    northern Maine
    Hey @Ben Howell

    Do you know if any mast cell experts have been invited to the August symposium?

    I have been learning about them over the past few months. The more I study the research, the more convinced I am that they play a major role in a subset of ME patients. Further, I have had substantial improvements in some symptoms since I started taking an antihistamine every day. For example, the hyperadrenergic POTS crashes and the itching on standing (or doing almost anything) have stopped.

    Here is an excerpt from Theoharides et al, "Chronic Fatigue Syndrome, Mast Cells, and Tricyclic Antidepressants", 2005:
    And here is another paper, "Brain fog", inflammation and obeisity: key aspects of neuropsychiatric disorders improved by luteolin", 2015:
    I don't know about anybody else, but Dr Theoharides and Dr Afrin (another mast cell expert) are two people I would very much like to talk to. Unfortunately it will never happen, because I don't have hives or anaphalaxis, so I can't get a referral to a mast cell expert, even though the research shows that half of mast cell patients don't have those symptoms. :bang-head:

    The idea of mast cell activation in ME fits in very nicely with Dr Naviaux's cell danger response theory. During his recent CDC talk he mentioned that cells under stress release ATP to signal other cells. Wanna guess one kind of cell that is activated by extracellular ATP? Yup. Mast cells.

    I don't think that ME is a mast cell disorder, or that treating mast cell problems will lead to recovery. But if mast cell disorder treatments can help our symptoms while Dr Davis and team find a real treatment, that would be a very good thing indeed.
     
    Gingergrrl, junkcrap50 and Nickster like this.
  3. NelliePledge

    NelliePledge plodder

    Messages:
    774
    Likes:
    3,516
    @Ben Howell can you post a link to this so we can repost it to facebook groups, other forums?
    cheers
     
    Jennifer J and Ben H like this.
  4. junkcrap50

    junkcrap50 Senior Member

    Messages:
    140
    Likes:
    163
    Hear, hear! I have research MCAS, MCAD, and Mast Cells and have reached the same conclusion. I think that it plays a significant role in CFS. It don't think it is the underlying cause or mechanism, but has a big affect on our symptoms as well as our inflammatory syndrome and cascade. So, I too would like to know if there are any mast cell experts invited as well.

    I believe that while a subset of CFS patients have obvious MCAS symptoms, there are many others that do not have typical MCAS symptoms while still having a mast cell issue. Having read Dr. Afrin's book, there are many cases that don't present as typical MCAS but have been successfully treated/cured with MCAS treatment.

    Fascinating that mast cells are activated by extracellular ATP. I'll have to research that. Perhaps you could send a tip to someone so that gets to Naviaux. (Dr. Theo also believes mast cells play a big role in autism, basically mast cell activation of the brain. So there is some research overlap between these two.)

    @jimells, I tried to make an appointment with Dr. Afrin, who didn't seem to need a referall or have a patient with hives/anaphylaxis, but he's booked up until into 2019.
     
    Gingergrrl likes this.
  5. Ben H

    Ben H OMF Correspondent

    Messages:
    771
    Likes:
    8,588
    U.K.
    Hi @NelliePledge

    It should be up here soon: https://www.omf.ngo/links-archives/

    If not feel free to copy and paste etc! Be sure to let people know they can sign up to the Newsletter and get it via email :)

    Thanks!

    B
     
    Jennifer J likes this.
  6. Ben H

    Ben H OMF Correspondent

    Messages:
    771
    Likes:
    8,588
    U.K.
    Hi @jimells @junkcrap50

    Certainly there will be scientists there with understanding of mast cells and the disease mechanisms, but Dr Theo and Dr Afrin will not be as they were not invited.

    I have read the research extensively of both the above (and others) since developing apparent MCAS and histamine issues, so know where you are coming from for sure. I'll mention it to Janet when we speak!


    B
     

See more popular forum discussions.

Share This Page