Special Episode: Part Two: Petition oral submission

Episode 6a - Carers Lived Experience with ME/CFS and long COVID - Know M.E.

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode features Steve Murray and Warren Tate speaking about their lived experience with caring for family/whanau with ME/CFS, and lived experience with long COVID.

Disclaimer: ANZMES does not benefit from or receive any funds from any courses or products mentioned in this podcast episode. ANZMES does not provide medical advice directly to patients. Please always seek professional medical advice. This podcast is intended for health professionals seeking information on how to help patients with these conditions.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: ⁠https://forms.gle/ntH67hkz2S5Jj8xt7⁠

For queries related to this Series contact: ⁠communications@anzmes.org.nz⁠

For general enquiries please contact: ⁠info@anzmes.org.nz⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠⁠www.anzmes.org.nz⁠⁠ or ⁠⁠www.givealittle.co.nz/org/anzmes⁠

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp #neuroplasticity #healing #chronicpain #fibromyalgia #longcovidkids #advocacy #longcovidawareness #mecfsawareness #DisabilityDenial

Episode 6 - Respiratory Medicine and Complementary Approaches for ME and lC - Know M.E.

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode features Tania Clifton-Smith and Megan Rodden speaking about respiratory medicine and complementary approaches for symptom management of ME/CFS and long COVID.

Disclaimer: ANZMES does not benefit from or receive any funds from any courses or products mentioned in this podcast episode. ANZMES does not provide medical advice directly to patients. Please always seek professional medical advice. This podcast is intended for health professionals seeking information on how to help patients with these conditions.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: ⁠https://forms.gle/ntH67hkz2S5Jj8xt7⁠

For queries related to this Series contact: ⁠communications@anzmes.org.nz⁠

For general enquiries please contact: ⁠info@anzmes.org.nz⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠⁠www.anzmes.org.nz⁠⁠ or ⁠⁠www.givealittle.co.nz/org/anzmes⁠

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp #neuroplasticity #healing #chronicpain #fibromyalgia #longcovidkids #advocacy #longcovidawareness #mecfsawareness #DisabilityDenial

Episode 5b - Fibromyalgia as a Teenager - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode features Emily Tuckey speaking about her lived experience with developing Fibromyalgia as a teenager, and includes a message for #teachers.

A full transcript is available here: ⁠https://docs.google.com/document/d/1enRAvmxkhdPnJHdB59uKSmgDLQwILMB17YBdv6j8Slc/edit?usp=sharing⁠

Disclaimer: ANZMES does not benefit from or receive any funds from any courses or products mentioned in this podcast episode. ANZMES does not provide medical advice directly to patients. Please always seek professional medical advice. This podcast is intended for health professionals seeking information on how to help patients with these conditions.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: ⁠https://forms.gle/ntH67hkz2S5Jj8xt7⁠

For queries related to this Series contact: ⁠communications@anzmes.org.nz⁠

For general enquiries please contact: ⁠info@anzmes.org.nz⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠⁠www.anzmes.org.nz⁠⁠ or ⁠⁠www.givealittle.co.nz/org/anzmes⁠

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp #neuroplasticity #healing #chronicpain #fibromyalgia #longcovidkids #advocacy #longcovidawareness #mecfsawareness #DisabilityDenial

Episode 5a - Lived experience Severe ME - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode features Wendy Matthews speaking about her lived experience with ME/CFS, and includes a message for government.

A full transcript is available here: https://docs.google.com/document/d/1enRAvmxkhdPnJHdB59uKSmgDLQwILMB17YBdv6j8Slc/edit?usp=sharing

Disclaimer: ANZMES does not benefit from or receive any funds from any courses or products mentioned in this podcast episode. ANZMES does not provide medical advice directly to patients. Please always seek professional medical advice. This podcast is intended for health professionals seeking information on how to help patients with these conditions.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

For queries related to this Series contact: communications@anzmes.org.nz

For general enquiries please contact: info@anzmes.org.nz

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp #neuroplasticity #healing #chronicpain #fibromyalgia #longcovidkids #advocacy #longcovidawareness #mecfsawareness #DisabilityDenial

Episode 5 - Lived and Professional Experience with ME, lC - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode features Dr. Asad Khan speaking about his personal and professional lived experience with ME/CFS, long COVID, MCAS, POTS, acute COVID wards, chronic illness in children and more.

A full transcript is available here: https://docs.google.com/document/d/1JfwrioqHDkFqN-hn_SqlC-P_ptHdqiI8X2-15jZ-73s/edit?usp=sharing

Disclaimer: ANZMES does not benefit from or receive any funds from any courses or products mentioned in this podcast episode. ANZMES does not provide medical advice directly to patients. Please always seek professional medical advice. This podcast is intended for health professionals seeking information on how to help patients with these conditions.

Links mentioned during the episode:

LinkTree: https://linktr.ee/doctorasadkhan

Long COVID Kids: https://www.longcovidkids.org/champions/dr.-asad-khan

Doctors with ME: https://doctorswith.me/

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

For queries related to this Series contact: communications@anzmes.org.nz

For general enquiries please contact: info@anzmes.org.nz

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp #neuroplasticity #healing #chronicpain #fibromyalgia #longcovidkids #advocacy #longcovidawareness #mecfsawareness #DisabilityDenial

Episode 4a - Symptom Management Strategies - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode features Dr. Eleanor Stein and Tessa Nielsen speaking about symptom management for ME/CFS, long COVID, Fibromyalgia, chronic pain, and more.

A full transcript is available here: https://docs.google.com/document/d/1ZWftjMZQHmi4rDTDCB6rBnqv_DPyoR6sAm62E0ARbLs/edit?usp=sharing

Disclaimer: ANZMES does not benefit from or receive any funds from any courses or products mentioned in this podcast episode. ANZMES does not provide medical advice directly to patients. Please always seek professional medical advice. This podcast is intended for health professionals seeking information on how to help patients with these conditions. Courses mentioned during the podcast:

Bounce Program by Specialised Health - https://www.specialisedhealth.nz/bounce-program

Dr. Eleanor Stein's

Pathways to Improvement: https://www.eleanorsteinmd.ca/pathways

Neuroplasticity: https://www.eleanorsteinmd.ca/pain

Alphabet Soup: http://www.eleanorsteinmd.ca/alphabet-soup

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

For queries related to this Series contact: communications@anzmes.org.nz

For general enquiries please contact: info@anzmes.org.nz

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp #neuroplasticity #healing #chronicpain #fibromyalgia

Episode 4 - GP Symptom Management - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode was recorded for ANZMES CME long COVID event held in November 2022. Dr. Ros Vallings discusses symptom management strategies for GPs.

It contains presentation slides which can be viewed on ANZMES YouTube channel here: ⁠⁠Know M.E. playlist⁠⁠

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

If you have questions related to this podcast, please contact communications@anzmes.org.nz

General enquiries: info@anzmes.org.nz

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp

Episode 3a - long COVID diagnosis - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

This episode was recorded for ANZMES CME long COVID event held in November 2022.

It contains presentation slides which can be viewed on ANZMES YouTube channel here: ⁠⁠Know M.E. playlist⁠⁠

A full transcript is available here: https://docs.google.com/document/d/1lOz0wW_n8UqgwF2z7Gh8EPFz_O--ZNWt2XDNGT_6To8/edit?usp=sharing

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp

Episode 3 - ME/CFS Diagnosis - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

In today's episode: ANZMES president Fiona Charlton speaks with RNZCGP Fellow Dr. Sarah Dalziel and Dr. Rosamund Vallings about diagnosing ME/CFS.

A full transcript of today's episode can be found here: https://docs.google.com/document/d/1PWp0HpfYn5ZC2WT5bS3sIwkIydd65tIkBO8O-gyrdlo/edit?usp=sharing

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

You can watch this as a vodcast here: ⁠Know M.E. playlist⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, support, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp

Coming up next

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

Find out about our next episode, due out June 8th.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

You can watch this as a vodcast here: ⁠Know M.E. playlist⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs

Special Episode: Part Two: Petition oral submission - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

In today's bonus episode: ANZMES president Fiona Charlton speaks with fellow ANZMES Executive Committee member Wendy Matthews, Emeritus Professor Warren Tate and RNZCGP Fellow Dr. Sarah Dalziel.

A full transcript of today's episode can be found here: https://docs.google.com/document/d/1n2a4h9B3NZrtcdfxnDs37wwr6L5T-znHhvMii9xuc2E/edit?usp=sharing

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

You can watch this as a vodcast here: ⁠Know M.E. playlist⁠

You can watch the oral submission to the Health Select Committee in Parliament here: https://fb.watch/khpmwwAaJR/ (minute: 39:29)

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp

Special Episode: Part One: ME/CFS, disability, and health equity - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

In today's episode: ANZMES president Fiona Charlton speaks with Dr. Neera Jain (University of Auckland) and Kate Waterworth (AUT University) about ME/CFS, disability, and health equity. A full transcript of today's episode can be found here: https://docs.google.com/document/d/1n2a4h9B3NZrtcdfxnDs37wwr6L5T-znHhvMii9xuc2E/edit?usp=sharing Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

You can watch this as a vodcast here: ⁠Know M.E. playlist⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs #disabilityinclusion #rnzcgp

Episode 2 - What is PEM and Pacing? - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

In today's episode: Dr. Lynette Hodges and Jen Mepham discuss Post Exertional Malaise (PEM) and Post Exertional Symptom Exacerbation (PESE) with ANZMES president Fiona Charlton.

PEM is the defining symptom of ME/CFS and is experienced by those with long COVID (LC).

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

A full transcript of today's episode can be found here: https://docs.google.com/document/d/1lZDcyiZFfT6ifi-HpdJjlieTWFpRJixCDRTdxvRNvgQ/edit?usp=sharing

You can watch this as a vodcast here: ⁠Know M.E. playlist⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy.

⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs

Toolkit for PEM - trailer

Toolkit for Post Exertional Malaise. Hear more from Jen Mepham and Dr. Lynette Hodges in Episode 2, due out May 11th. Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E. Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: ⁠https://forms.gle/ntH67hkz2S5Jj8xt7⁠ You can watch this as a vodcast on: https://www.youtube.com/playlist?list=PLlV7biMCtpYDdldX5H94-cJrEIUAsgzU1 ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education. ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy. ⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes #myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs

Dysfunction not deconditioning - trailer

Dysfunction not deconditioning. Hear or watch the full episode with Dr. Lynette Hodges and Jen Mepham on May 11th.

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: ⁠https://forms.gle/ntH67hkz2S5Jj8xt7

⁠You can watch this as a vodcast at: https://youtu.be/yyaU27tg4so

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy. ⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs

Stay tuned for our Special Episode

Find out more about our Special Episode for May - ME/CFS Awareness Month, due on May 11th.

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: ⁠https://forms.gle/ntH67hkz2S5Jj8xt7⁠

You can watch this as a vodcast here: ⁠Know M.E. playlist⁠

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy. ⁠www.anzmes.org.nz⁠ or ⁠www.givealittle.co.nz/org/anzmes

#myalgicencephalomyelitis #chronicfatiguesyndrome #longcovid #knowme #knowmenz #anzmes #longcovidrecovery #disability #healthequity #medicaleducation #continuingmedicaleducation #mecfs

Up next ... PEM and pacing

Find out more about Episode 2, due out May 11th.

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

You can watch this as a vodcast here: Know M.E. playlist

ANZMES is the national advisory for ME/CFS in Aotearoa/New Zealand. ANZMES offers representation, information, national level support, and research funding. ANZMES is a RNZCGP registered provider for continuing education.

ANZMES is a nonprofit relying on the generosity of donors to continue its vital services. All executive committee members are unpaid volunteers. Donate today through the link provided so that ANZMES can continue crucial education, research, and advocacy. www.anzmes.org.nz or www.givealittle.co.nz/org/anzmes

Episode 1 - What is ME/CFS? - Know M.E. Series

Know M.E. the podcast where guest speakers talk about pressing issues surrounding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post COVID Conditions. Join researchers, clinicians, and patient advocates as we take a deep dive into the most recent, evidence-based information, so that you too can know M.E.

In today's episode: We will discuss ME/CFS and long COVID, covering classifications and symptomology. We're joined by the 2 most well known names in New Zealand, in relation to M.E.: Emeritus Professor Warren Tate and Dr. Rosamund Vallings.

Professor Tate has been an academic and researcher at the University of Otago in Dunedin for 55 years. Dr. Rosamund Vallings has seen patients with ME/CFS for the past 40 years.

Health professionals can earn CME credits as they listen by subscribing to Know M.E. news at: https://forms.gle/ntH67hkz2S5Jj8xt7

A full transcript of today's episode can be found here: https://docs.google.com/document/d/129u3yDDOOW5_aIF2P3SZHBb_oZ_-xTYBMpSLgRz8UBA/edit?usp=sharing

You can watch this as a vodcast here: https://youtu.be/xvqVkq4JNXM

Know M.E.

By Know ME

Available on