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 Professor Warren Tate speaking about international and Aotearoa / New Zealand biomedical research and understanding 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: ⁠⁠[email protected]⁠⁠ For general enquiries please contact: ⁠⁠[email protected]⁠⁠ 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

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. Sarah Dalziel discussing dysautonomia and research findings. This presentation with slides was recorded for an ANZMES event in September 2022. 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: ⁠[email protected]⁠ For general enquiries please contact: ⁠[email protected]⁠ 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

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: ⁠[email protected]⁠ For general enquiries please contact: ⁠[email protected]⁠ 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

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: ⁠[email protected]⁠ For general enquiries please contact: ⁠[email protected]⁠ 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

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: ⁠[email protected]⁠ For general enquiries please contact: ⁠[email protected]⁠ 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

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: [email protected] For general enquiries please contact: [email protected] 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

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: [email protected] For general enquiries please contact: [email protected] 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

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: [email protected] For general enquiries please contact: [email protected] 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

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 [email protected] General enquiries: [email protected] 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

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