The NBA Today crew discusses LeBron James’ injury, the Los Angeles Lakers’ expectations in his absence, and Steph Curry nearing the milestone of 4,000 career three-pointers.
0:00 Lakers vs. Celtics recap
2:15 LeBron James’ injury
3:00 What are the Lakers’ expectations without LeBron?
4:10 How concerning is LeBron’s injury?
6:40 Pistons vs. Warriors recap
7:30 Will Curry reach 4,000 career three-pointers vs. Trail Blazers?
10:15 Jimmy Butler’s impact
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Pardon the Interruption | LeBron James’ injury could affect Lakers’ standings – Michael Wilbon
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Vascular Ehlers-Danlos syndrome (vEDS) is a dominantly inherited, genetic connective tissue disorder. vEDS is particularly serious because of the risk for spontaneous arterial or organ rupture.
Potentially fatal effects include arterial aneurysm, dissection, and rupture; bowel rupture; and rupture of the uterus when pregnant. Life span is often affected.
This awareness video hopes to highlight some of the experiences of the community living with vEDS, the impact on their families, the importance of education and research, and hopes for the future. There is no better way of hearing what it is like to live with vEDS, than from individuals who have vEDS themselves.
The Ehlers-Danlos Society is proud to be a member of The Vascular Ehlers-Danlos Syndrome Collaborative, a group of patients, family members, researchers, and clinicians, dedicated to developing a patient-centered plan for scientific research, to improve the management of vEDS, and to increase the quality of life for all those impacted by the condition.
A vEDS diagnosis is most often sought because of family history; someone’s medical history; or pregnancy complications at a young age. Confirmation helps rule out other possible causes for symptoms as well as establishing a clear need for medical surveillance, treatment, and study of family members.
After diagnosis, the first priority is assembling an integrated care team to provide a clinical and social support network for the individual and their family. Management is complex and requires multiple specialists who can respond to and manage major complications.
In 2019, The Ehlers-Danlos Society launched vEDS ECHO: a program led by Dr. Sherene Shalhub dedicated to increasing awareness and education in all aspects of diagnosis and management of vEDS.
VEDS ECHO is a revolutionary program that seeks to support health professionals around the world in caring for patients with vEDS. Clinical experts run a program that covers the main aspects of vEDS. Participants are able to share their cases and questions in the sessions and are guided to further educational materials and support. Continued Medical Education (CME) credits are available at no charge to participants. https://www.ehlers-danlos.com/project-veds-echo/
The Ehlers-Danlos Society offers monthly virtual support groups for those living with vEDS and their families, and also a group dedicated to parents; those who have vEDS and those who have children with vEDS. https://www.ehlers-danlos.com/virtual-support/
We are delighted to be hosting a dedicated event for vascular Ehlers-Danlos syndrome (vEDS) on July 31, 2021. Join us as leading experts present the latest research, management, and scientific information on vEDS and comorbidities. We will be offering live translations during this event in English (original language), French, German, Spanish, and Japanese. Register and learn more here: https://www.ehlers-danlos.com/eds-echo-event-series-vascular-ehlers-danlos-syndromes/
Much more awareness is needed of this type of Ehlers-Danlos syndrome, it is important that health professionals are educated in the presentation of vEDS, genetics and familial impact, possible implications and surgical interventions, and treatment guidance. The Ehlers-Danlos Society is committed to improving the lives of those impacted by vEDS, and facilitating global awareness and education. Our strength begins with hope. ehlers-danlos.com Video Rating: / 5
(Visit: http://www.uctv.tv/) Dr. Christina Allen, UCSF Department of Orthopaedic Surgery, Division of Sports Medicine, discusses the causes, diagnosis, and possible treatment options for different types of traumatic knee injuries. Injuries may range from meniscus tears and ligament injuries, to cartilage and tendon injuries. Recorded on 03/11/2014. Series: “UCSF Osher Center for Integrative Medicine presents Mini Medical School for the Public” [5/2014] [Health and Medicine] [Show ID: 27892] Video Rating: / 5
Hypertension and blood pressure issues are becoming ever more prevalent in the world. In this video, Sadhguru offers six time-tested, natural and drug-free remedies that can help prevent and regulate high blood pressure and hypertension.
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Patricia Weltin of Beyond the Diagnosis talks about Elhers-Danlos syndrome, a rare disease that afflicts two of her daughters.
Ehlers-Danlos syndrome is a group of connective tissue disorders. There are various forms of Ehlers-Danlos. According to the NIH, there are numerous types of Ehlers-Danlos syndrome had been described and to date, over 19 genes have been associated with this disease. Most of those genes (COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, ADAMTS2, FKBP14, PLOD1, and TNXB) are linked directly or indirectly to collagen production.
A common symptom in most people with Ehlers-Danlos syndrome is an unusually large range of joint movement (hypermobility). While often viewed as an interesting school yard trick, the loose joints are unstable and prone to dislocation and chronic pain.
Many people with the Ehlers-Danlos syndrome also have soft, velvety skin that is elastic and fragile. Organ damage and bone abnormalities can also be observed in these patients.
As Weltin explains in this video, her daughters grew up relatively normal but as soon as puberty began, aches, pains, and joint dislocations became more commonplace.
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Dr. Anand Saggar describes the complexity of Ehlers-Danlos syndrome. Likening it to the mythological creature of the hydra, Dr. Saggar cautions that EDS has “many heads”, and it can affect individuals in vastly different ways.
Dr. Saggar goes on to explain just how common connective tissue disorders can be in patients with other disorders and even in the general population. He emphasizes the importance of genetic testing to confirm diagnoses of connective tissue disorders.
This lecture was presented at the 2019 London Roundtable provided in partnership with the Ehlers-Danlos Society, focusing on issues surrounding dysautonomia, connective tissue disorders, Chiari malformation and related syndromes. (2019)
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See Caleb’s hilarious reaction after waking up from his operation! Isaac and Elise go to a Royals MLB game and Baby Janae tests out her squeaky shoes!
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Welcome to J House – an imperfect family working together towards a happy home filled with love and meaningful connections. We focus on learning, serving, and playing together as a family. We (Jeremy and Kendra) have 5 little kids: Isaac, Elise, Caleb, Laura, and Janae.
Our original vlog channel: J House Vlogs https://youtube.com/jhousevlogs documents our family life. J House jr. takes highlights of our favorite memories and makes them more entertaining for kids! Expect to see a lot of kids playing, laughing, and learning together! We also make original videos here that we think are perfect for kids! Video Rating: / 5
