Find A Cure Club
  • Find A Cure Club
    • How Find A Cure Works
    • FACC Meetings
    • Insured? Think Again
    • What is it Like to live with M.E?
  • URGENT Help Needed
  • Superannuation & Insurance
  • Join the NDIS
  • FACC News
    • Your Questions
  • International ME Awareness 2012
    • ARCHIVES
  • Media Help Needed ... May 2012
  • Prizes
    • Australian feedback on Voices from the Shadows
  • Awareness Around the World 2012
  • Advocacy Tools
    • House Bound Advocacy
  • ALISON HUNTER MEMORIAL FOUNDATION
    • LOST VOICES
  • Invest In Me
    • Everyday Heroes
  • ESME
  • Stanford School of Medicine
  • THE ADVOCATES
  • TARA Has M.E
    • Treatment Guidelines Fail Patients
  • Research Agenda's 2012
  • Friends on the Coast
    • Aussie Support Connections
  • Fundraising for M.E Research
  • NEED HELP?
    • TeleHealth
    • Blue Care Caloundra
    • The Best Doctors
    • TREATMENTS
    • Medical Interventions
    • Medicinal Supplements
  • Help is Available in Queensland through Blue Care
  • Health Impact of M.E
  • LOCAL HEALTH SERVICES
    • Wheelchairs
    • Optometrists
    • LOCAL BUSINESS
  • AFTER HOURS MEDICAL ASSISTANCE
  • NEEDING TRANSPORT
  • Notices
  • Participate in Australian Research
  • Clinical Trials
    • Ampligen
  • Pediatric Research
  • Be Our Champion
    • Angel of Hope
    • Voices from the Shadows
  • When Medical Practices Fail Us
    • DIAGNOSTIC MARKER
  • Heart Problems in M.E
    • Echocardiogram
    • Diastolic Dysfunction and Diastolic Heart Failure
  • EXERCISE Problems in M.E
  • We Endure Cancer / Organ Failure & Medical Neglect
  • Self Help
    • Lymphatic Drainage
  • SNAP NEWS
    • Blog Links
    • The Stuff of Nightmares
  • GLOBAL ADVOCACY NETWORK
  • MEDIA INFORMATION
    • Diseased & Dying go Unassisted
    • GOVERNMENT HEALTH SYSTEMS ARE FAILING ME CFS
    • MEDIA HELPS RIGHT THE WRONG
    • HERE WE ARE ... HELP US
    • M.E OUTBREAKS
    • M.E Documentary
    • Is There a Doctor in the House?
  • EDUCATION
    • A Bit Of History Repeating
    • Testimonies
  • RESEARCH FINDINGS
    • TRIALS OF ANTIVIRALS IN CFS SUBGROUPS
    • Researching CFS Subgroups
  • WHY CFS SUBGROUP DISEASES ARE NOT TREATED
  • XMRV RESEARCH
  • M.E RESEARCH ARTICLES
    • Drugs - Urgently Needed
    • Assays Developed
  • Multiple Chemical Sensitivity
  • LYME Disease
    • Diagnosing Lyme & Co Infections
    • Lyme Blogs
  • A Quilt For The Prime Minister
    • Quilt Blocks
    • Australian Stories
    • Instuctions For Quilt
    • What is Your States Colour?
    • Finished Block
    • Iron on Backing
    • Your Name
  • MAPAN
  • Children with MEcfs
    • A Better Way OF Doing Things
    • NOWHERE TO TURN
    • Electric Wheelchairs
    • The Storm in the Tea Cup
    • Prose Advocacy
  • HEALTH BASICS
    • LIVER HEALTH
  • Doctors Worldwide
    • Jose G Montoya MD
    • Dr Anthony Komaroff
  • Bond University
  • The Norwegian Study of CFS
  • 1980's CDC Investigations
  • Australian Government
    • Nicola Roxon
    • Government Funding
    • How to Improve CFS Disability
  • Australian MEcfs Organisations
  • Local Suburban Support Groups
    • NEW SOUTH WALES
    • Support and Validation
    • WHAT YOU SAY
  • Awareness Events
    • ART AWARENESS
    • ART COLLECTIONS
    • Organising an Awareness Event
    • ME CFS FM CARTOONIST
  • Rags For Research
    • The Research Shop
  • COMMUNITY LINK - UP
  • KIDS CORNER
  • Carers Unite
  • ASD
    • Autism IN Research
  • Need Some Answers
  • MEMORIAL PAGE
    • IN LOVING MEMORY

Dignity in Health and Sickness

The Find a Cure Club is a support service for people with Myalgic Encephalomyelitis M.E and Fibromyalgia FM

We are based on the Sunshine Coast in Queensland, Australia.

Our Mission is to support individuals with information and to help raise Awareness of ME and FM within your local Communities through collaboration and Cooperation.

If you need assistance with Awareness in your area, please give us a call.




                        Now All We Need Is YOU


There is mounting evidence that Myalgic Encephalomyelitis  is associated with cardiovascular complications … including autonomic dysfunction, impaired blood pressure regulation and loss of beat-to-beat heart rate control.

Research shows raised levels of oxidative stress, low-grade inflammation and increased arterial stiffness contribute to increased cardiovascular risk for people with M.E


Picture
" It is Time to Tell it Like it Really Is"
" There are two important things that we’ve found, an abnormal level of an inflammatory chemical in the blood, and abnormal white blood cell behaviour …"
These Poster Leaflets are available in packs of 10
 
The Young ME Sufferers Trust       PO Box 4347, Stock, Essex, CM4 9TE

Jane Colby FRSA
Executive Director





Australia's Alison Hunter died in 1996, aged 19, from Myalgic Encephalomyelitis, which included seizures, paralysis, gastrointestinal paresis and overwhelming infections ... 

One of Alison's Australian Doctors wrote in a letter 

" ... I grieve that I was not able to relieve her suffering or turn back the monstrous illness which overwhelmed her and which robbed her of so much of her life.  

It was a privilege to know her but also a very humbling experience and to know that ALL our assembled medicine was pitifully inadequate. "

Emily Rose Collingridge died this year 2012, aged 30, from Myalgic Encephalomyelitis

VICTORIA WEBSTER dies aged 18 from Cardiac Arrest due to M.E


People with M.E are left to struggle, suffer, linger and die prematurely.  

  When will our Government step in and make M.E Research a Priority?  




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    CONTACT  Lesley McLeod

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