The agmdhope’s Podcast
AGMD is proud to sponsor podcasts on various digestive motility and neurogastroenterology topics. Guests inclulde medical, scientific, and nutritional experts along with patients, family members, and caregivers.
AGMD is proud to sponsor podcasts on various digestive motility and neurogastroenterology topics. Guests inclulde medical, scientific, and nutritional experts along with patients, family members, and caregivers.
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Episodes

Jan 16, 2019
Jan 16, 2019
1 hr 1 min
AGMD presents its Young Adult Telephone Internet Community Support Group meeting. This meeting is co-facilitated by Andrew Carbone, a young adult patient with chronic intestinal pseudo-obstruction, gastroparesis and gastroesophageal reflux disease.
All participants have consented to AGMD to have their voices recorded during the program should they decide to speak.
Jan 16, 2019
1 hr 1 min
Jan 16, 2019
Jan 16, 2019
59 min
Parents with a child of any age suffering from a digestive motility disease or disorder need support. Our Telephone Internet Community Support Group program provides a forum for parents to share their questions, concerns, frustrations, and emotions with others who understand.
All participants gave their permission for their voices to be recorded if they chose to speak during the program.
Jan 16, 2019
59 min

Jan 15, 2019
Jan 15, 2019
1 hr 1 sec
The Association of Gastrointestinal Motility Disorders, Inc. (AGMD) presents, Living With Digestive Motility Disorders. This open discussion meeting is for anyone affected by motility disease, including patients, parents, partners, and loved ones. AGMD provides a safe place to talk about everything that goes along with the diagnosis of a motility disease. Topics include emotional/mental health issues, chronic pain, relationships (personal as well as with medical professionals) ostomies, tubes, lines, and nutrition.
This program is co-facilitated by Brittany Neal. Brittany is a patient with chronic idiopathic pseudo-obstruction since birth. Now in her 30s, she has had numerous surgeries and procedures including multiple central liine placements, G and J-tubes, and has a permanent ileostomy. She is currently TPN dependent and has several health concerns due to CIPO. No longer able to work, she serves as a volunteer for AGMD.
Since the publication of this program, we sadly report that Brittany Neal passed away in February 2018. She is greatly missed. We honor her memory by posting this program. It reflects her caring heart and unconditional dedication and willingness to help others.
Jan 15, 2019
1 hr 1 sec

Jan 14, 2019
Jan 14, 2019
54 min
AGMD Presents its Patient Telephone Internet Community Support Group meeting.
This forum provides a place for patients as well as their family members, to voice their concerns, frustrations, share their experiences and gain much needed support.
All program participants have given their consent to AGMD for their voices to be recorded should they decide to speak during the program.
Sponsored by the Association of Gastrointestinal Motility Disorders, Inc. | AGMD |
Jan 14, 2019
54 min

Jan 14, 2019
Jan 14, 2019
1 hr 4 min
AGMD presents its Gastroparesis Telephone Internet Community Support Group meeting.
This program provides a forum for patients and their loved ones to share their questions, concerns and frustrations and receive much needed support.
All participants gave AGMD their consent to be recorded if they chose to speak during the program.
Jan 14, 2019
1 hr 4 min

Jan 14, 2019
Jan 14, 2019
52 min
AGMD presents its Chronic Intestinal Pseudo-Obstruction (CIPO) Telephone Internet Community Support Group meeting. This forum provides a place for patients with CIPO as well as their family members, to voice their concerns, frustrations, share their experiences and gain much needed support.
All program participants have given their consent to AGMD for their voices to be recorded should they decide to speak during the program.
Jan 14, 2019
52 min

Jan 14, 2019
Jan 14, 2019
59 min
AGMD Presents its Patient Telephone Internet Community Support Group meeting.
This forum provides a place for patients as well as their family members, to voice their concerns, frustrations, share their experiences and gain much needed support.
All program participants have given their consent to AGMD for their voices to be recorded should they decide to speak during the program.
Jan 14, 2019
59 min

Jan 13, 2019
Jan 13, 2019
1 hr 8 min
The Association of Gastrointestinal Motility Disorders (AGMD) is privileged to present An interview featuring Jaime, a parent who has a child with Hirschsprung's Disease. During the program, Jaime chronicles her heart-warming and moving journey as she describes life with a child having Hirschsprung's Disease.
Sponsored by the Association of Gastrointestinal Motility Disorders, Inc. (AGMD).
Jan 13, 2019
1 hr 8 min

LEARN, SHARE, AND BE INSPIRED!
AGMD is a nonprofit international organization that serves as an integral educational resource for digestive motility diseases and disorders. It also functions as an important information clearinghouse for members of the medical, scientific and nutritional communities. In addition, AGMD provides a forum of support for patients (and their families) suffering from digestive motility diseases and disorders.
We are honored to sponsor our podcasts in order to educate, advocate, and inspire!
To learn more about AGMD visit our website at www.agmdhope.org


