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What are the latest advances in Chronic Fatigue Syndrome / M.E.?

Here you can see the latest advances and discoveries made regarding Chronic Fatigue Syndrome / M.E..

Latest progress of Chronic Fatigue Syndrome / M.E.

Chronic Fatigue Syndrome (CFS), also known as Myalgic Encephalomyelitis (ME), is a complex and debilitating condition characterized by extreme fatigue that cannot be explained by any underlying medical condition. While the exact cause of CFS/ME remains unknown, researchers have made significant advancements in understanding and managing this condition.

Diagnostic Criteria:
One of the recent advances in CFS/ME is the development of updated diagnostic criteria. In 2015, the Institute of Medicine (now known as the National Academy of Medicine) released a report that proposed a new set of diagnostic criteria called the Systemic Exertion Intolerance Disease (SEID) criteria. These criteria emphasize the core symptoms of CFS/ME, including post-exertional malaise, unrefreshing sleep, cognitive impairment, and orthostatic intolerance. The SEID criteria aim to improve the accuracy of diagnosis and ensure that individuals with CFS/ME receive appropriate care.

Biological Markers:
Researchers have been actively investigating potential biological markers for CFS/ME to aid in diagnosis and understanding of the underlying mechanisms. Several studies have identified abnormalities in immune system function, including increased levels of inflammatory markers and alterations in cytokine profiles. Additionally, abnormalities in the hypothalamic-pituitary-adrenal (HPA) axis, which regulates stress response, have been observed. These findings provide valuable insights into the biological basis of CFS/ME and may lead to the development of targeted treatments in the future.

Immunological Abnormalities:
Advancements in immunological research have shed light on the role of the immune system in CFS/ME. Studies have shown alterations in natural killer (NK) cell function, T-cell subsets, and cytokine profiles in individuals with CFS/ME. These findings suggest that immune dysregulation may contribute to the pathophysiology of the condition. Furthermore, recent research has explored the potential involvement of autoimmunity in CFS/ME, with some studies identifying autoantibodies targeting specific receptors or ion channels. These discoveries open up new avenues for therapeutic interventions targeting the immune system.

Neurological Findings:
Emerging evidence suggests that CFS/ME may involve neurological abnormalities. Neuroimaging studies have revealed structural and functional differences in the brains of individuals with CFS/ME compared to healthy controls. These differences primarily involve regions associated with pain processing, fatigue, and cognitive function. Furthermore, abnormalities in the autonomic nervous system, such as reduced heart rate variability and orthostatic intolerance, have been observed. Understanding the neurological aspects of CFS/ME is crucial for developing targeted treatments and interventions.

Treatment Approaches:
While there is currently no cure for CFS/ME, treatment approaches have evolved to focus on symptom management and improving quality of life. Graded exercise therapy (GET) and cognitive-behavioral therapy (CBT) have been commonly used interventions, although their effectiveness and appropriateness for all individuals with CFS/ME have been subjects of debate. Recently, there has been a shift towards individualized and multidisciplinary approaches that address the unique needs of each patient. This may include pacing strategies, energy management techniques, dietary modifications, and complementary therapies such as acupuncture or mindfulness-based interventions.

In conclusion, significant progress has been made in understanding and managing Chronic Fatigue Syndrome/Myalgic Encephalomyelitis. Advances in diagnostic criteria, identification of biological markers, immunological and neurological research, and evolving treatment approaches have provided valuable insights into this complex condition. Continued research efforts are essential to unravel the underlying mechanisms, develop targeted therapies, and ultimately improve the lives of individuals living with CFS/ME.
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13 answers
I don't know any...My last visti was a year ago. I did not have any new indication or medication...

Posted Aug 27, 2017 by Emy 2050
This is where it gets exciting!! Rituximab is on a large scale trial in Norway, there's interesting stuff about gut microbiota in Norwich, and B cell stuff in London, and similar stuff in the USA.

Posted Sep 5, 2017 by Shirley 2050
Open Medicine Foundation (www.omf.ngo) is our best hope. I support them because the two lead founders (Prof Ron Davis & Linda Tannenbaum) both have children suffering from ME/CFS. They have assembled global Nobel Laureates & Academy of Science members to collaboratively fast track research for a biomarker, treatment & cure. Based in Stanford CA USA. A friend-fellow patient & I started an awareness/fundraisier called Join M.E. in #SillySheets: pose & post your silliest, in bed, selfie on social media (in solidarity with extreme ME/CFS, bedridden & very private patient, Whitney Dafoe son of Prof Ron Davis at OMF) OR donate to www.omf.ngo within 24 hours. Then nominate 3 others to do the same. #SillySheets #EndMECFS

Posted Sep 7, 2017 by 2560
There are at present many resarch programmes and new clues privately funded by sufferers family and friends
Im hopeful but cant tell u what they are
Im ill with head fog

Posted Jan 17, 2018 by Annette 2500
Health Rising is a good source, such as this one:

https://www.healthrising.org/blog/2018/02/08/cortene-way-new-drug-trialed-chronic-fatigue-syndrome-mecfs-soon-pt/

Posted Mar 3, 2018 by Beti 2700
Summary:
A study has identified a constellation of metabolites related to myalgic encephalomyelitis/chronic fatigue syndrome.

Posted Aug 9, 2018 by cathy 2500
there are one of either as of yet, just rehashes of science from the 80s and 90s
that being said our patient community is stronger than ever before
so there is hope for better care

Posted Apr 6, 2019 by Fadra 2550
Please see this video for more info: https://www.facebook.com/ChemicalsAndChronicIllness/videos/482283219312338

Posted Dec 12, 2019 by Joanna 6200
Some are thinking a biomarker will be coming soon but as of now just rest, pacing and perhaps LDN.

Posted Dec 21, 2019 by Pam 3550
Translated from spanish Improve translation
There is much talk of genetics, but there is nothing of nothing at the moment.

Posted Sep 11, 2017 by Eduardo Casasnovas 2950
Translated from spanish Improve translation
Drug in oil, smoke comes out cheaper.

Posted Sep 11, 2017 by Haydee de bielik 5120
Translated from spanish Improve translation
As I already said, they are investigating on the dysfunction of the mitochondria in a study of patients and healthy subjects.
We also apply more studies in nuclear medicine, the disadvantage is the high cost.
Attached are the research on the hereditary factor.

Posted Oct 19, 2017 by Heidrun Kroner 2000

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CHRONIC FATIGUE SYNDROME / M.E. STORIES
Chronic Fatigue Syndrome / M.E. stories
Mine is a story of gradual onset MECFS.  I was in my late twenties when my life began to 'not make sense'.   This was in 1976. I had always been active in sports and was fully engaged in being a wife and mother of two young preschool children.  M...
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Mold Warriors by Dr Ritchie Shoemaker Gateway Press 2005 Chapt. 23 Mold at Ground Zero for CFS   The history of Chronic Fatigue Syndrome (CFS) begins in Incline Village, Nevada in 1985. In the medical history of CFS, each of the concepts applies-...
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I wish that more MDs thought more carefully about CVID, PANS/PANDAS and EDS/MCAS.  If I had been diagnosed and treated earlier in life with Igs (instead of being called a hypochondriac and shuffled off to conventional psychiatry), I may not have end...
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I was your typical average teenage girl always out running around. always out scaring my parents because yet again i was doing something crazy like climbing a really high tree, or riding my bike to close to the duck pond, or going fishing and forgeti...
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Hi all Here is my story.... I started having problems with my knees when I was about 11yrs old, docs just thought it was growing pains and all they did was give me antiinflammatories. As I approached my mid teens I started sleeping in class althoug...

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CHRONIC FATIGUE SYNDROME / M.E. FORUM
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Have you used Colloidal Gold and if so is it helping you at all?
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 LBL did study of CO2 in air on thought and finds quite surprisingly, thought gets much worse if CO2 in outside air of 400ppmv, goes up from exhaled breath at 40,000 ppm, to raise room ambient to 1000ppmv or greater. Free reference: http://...

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