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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: [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
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By Know MEKnow 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