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Ehlers-Danlos syndromes: Current landscape and hopes for future directions
MP3•Episode home
Manage episode 286187532 series 2543578
Content provided by Pain Waves by Pain BC. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Pain Waves by Pain BC or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Ehlers-Danlos syndromes (EDS) are thirteen subtypes of rare connective tissue disorders characterized by numerous debilitating symptoms, including chronic pain. Sadly, current gaps in dedicated health care and research for EDS leave many Canadians living with these chronic illnesses undiagnosed or undertreated.
On this month’s episode of the Pain Waves podcast, we’re joined by three guests to learn more about these chronic illnesses. Dr. Nimish Mittal tells us about what Ehlers-Danlos syndromes are, the current gaps in health care and research, and what changes need to be made in the Canadian health care system to better support people living with EDS. We’re also joined by Kathleen Eubanks from EDS Canada, who shares her firsthand experience of living with the illness, and Sandy Smeenk from the ILC Foundation, who shares her professional and personal experiences as a mother to a child with EDS.
Resources mentioned in this episode:
- EDS Society: https://www.ehlers-danlos.com/
- EDS Canada: https://ehlers-danlossyndromecanada.org/
- The ILC Foundation: https://www.theilcfoundation.org/
- GoodHope EDS Clinic: https://www.uhn.ca/MCC/Clinics/Ehlers-Danlos_Syndrome_Clinic
…
continue reading
On this month’s episode of the Pain Waves podcast, we’re joined by three guests to learn more about these chronic illnesses. Dr. Nimish Mittal tells us about what Ehlers-Danlos syndromes are, the current gaps in health care and research, and what changes need to be made in the Canadian health care system to better support people living with EDS. We’re also joined by Kathleen Eubanks from EDS Canada, who shares her firsthand experience of living with the illness, and Sandy Smeenk from the ILC Foundation, who shares her professional and personal experiences as a mother to a child with EDS.
Resources mentioned in this episode:
- EDS Society: https://www.ehlers-danlos.com/
- EDS Canada: https://ehlers-danlossyndromecanada.org/
- The ILC Foundation: https://www.theilcfoundation.org/
- GoodHope EDS Clinic: https://www.uhn.ca/MCC/Clinics/Ehlers-Danlos_Syndrome_Clinic
92 episodes
MP3•Episode home
Manage episode 286187532 series 2543578
Content provided by Pain Waves by Pain BC. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Pain Waves by Pain BC or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Ehlers-Danlos syndromes (EDS) are thirteen subtypes of rare connective tissue disorders characterized by numerous debilitating symptoms, including chronic pain. Sadly, current gaps in dedicated health care and research for EDS leave many Canadians living with these chronic illnesses undiagnosed or undertreated.
On this month’s episode of the Pain Waves podcast, we’re joined by three guests to learn more about these chronic illnesses. Dr. Nimish Mittal tells us about what Ehlers-Danlos syndromes are, the current gaps in health care and research, and what changes need to be made in the Canadian health care system to better support people living with EDS. We’re also joined by Kathleen Eubanks from EDS Canada, who shares her firsthand experience of living with the illness, and Sandy Smeenk from the ILC Foundation, who shares her professional and personal experiences as a mother to a child with EDS.
Resources mentioned in this episode:
- EDS Society: https://www.ehlers-danlos.com/
- EDS Canada: https://ehlers-danlossyndromecanada.org/
- The ILC Foundation: https://www.theilcfoundation.org/
- GoodHope EDS Clinic: https://www.uhn.ca/MCC/Clinics/Ehlers-Danlos_Syndrome_Clinic
…
continue reading
On this month’s episode of the Pain Waves podcast, we’re joined by three guests to learn more about these chronic illnesses. Dr. Nimish Mittal tells us about what Ehlers-Danlos syndromes are, the current gaps in health care and research, and what changes need to be made in the Canadian health care system to better support people living with EDS. We’re also joined by Kathleen Eubanks from EDS Canada, who shares her firsthand experience of living with the illness, and Sandy Smeenk from the ILC Foundation, who shares her professional and personal experiences as a mother to a child with EDS.
Resources mentioned in this episode:
- EDS Society: https://www.ehlers-danlos.com/
- EDS Canada: https://ehlers-danlossyndromecanada.org/
- The ILC Foundation: https://www.theilcfoundation.org/
- GoodHope EDS Clinic: https://www.uhn.ca/MCC/Clinics/Ehlers-Danlos_Syndrome_Clinic
92 episodes
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