SORT BY Relevancy
First time I talked to Sherly, she told me that she had once been a teacher but hasn't been able to work FT in decades. She has had Lymphedema since in the early 90s. She has difficulty fulfilling her life, difficulty in transportation. She has no way of getting a compression garment (which can cost $500) without having to choose between a garment or paying rent because her income is just that stressed already. Complicated by tumors (one removed and another that needs to removed). She has written her Represenative but hasn't had a response just yet. Hopefully, he'll get on board with the Lymphedema Treatment Act which will authorize Medicare to pay for the garment that helps to keep the lymphedema from getting worse, which causes so many other dominoing issues (like mobility, possible MS, and other diseases that stem from the damaged lymphatic systerm.
In Texas, we have 3 co-sponsors for the Lymphedema Treatment Act, and we have many more to go. There are 4 bipartisan leads and 99 co-sponsors of the Lymphedemat Treatment Act across the United States. We really need about 200 co-sponsors for this bill to be passed in the House. We need your support to help the many Sheryl's out there with similar stories. Please go to the http://lymphedematreatmentact.org website to sign up being a Team Member in your State and go to the "How You Can Help" and send your legislators personalize letters.
Listen to the show that we had on November 20th as well for some other call to actions that you can do to help.
#LymphedemaTreatmentAct #LymphedemaStory #Project1000000Voice
I have done several shows about Lymphedema and the grassroots efforts to get the Lymphedema Treatment Bill passed. This one came from an original airing of 5/1/10.
"Back in March, we had a show introducting you to the HR 4662 which involves the improvement for health care costs for lymphedema patients. Please join us again today to learn what has been done, what you can do, and what this means to you if you (or someone you know) has lymphedema. We need to get this bill passed in this year's legislation session. We will have Jennifer and Jenny on our show, as well as some other pertinent people that can add more to enlighten about this very important bill." http://www.blogtalkradio.com/oralhistory/2010/05/01/beyond-words-live--understanding-hb-4662
BEYOND WORDS LIVE is designed as a platform for survivors to tell their own stories in their own words.
For more information see http://facebook.com/LymphedemaInTheNews or http://lymphedematreatmentact.org/.
In September 2014, a group of lymphedema advocates converged upon the Capitol Hill to talk to the US House of Represenatives and Senators about the Lymphedema Treatment Act, as well as had a Congressional Hearing to empasize the importance that it means to many lymphedema patients, caregivers, physicians, and more. As a result, we ended up with 4 bipartisan lead sponsors from the House of Represenatives, and 91 cosponsors from many of the States. We really need about 200 cosponsors to help ensure that this Bill passes the House.
Guidance was provided by the Lymphedema Advocacy Group, National Lymphedema Network, and many other supporters of the Bill.
Join us on our Lymphedema Journey and Advocacy for a discussion on a reflection of those this year's journey at Capitol Hill (DC) and a call of action that we would like for you to do as soon as possible.
For many more details about the Lymphedema Treatment Act, please check out the website http://lymphedematreatmentact.org.
Also check out the Lymphedema In The News fb page http://facebook.com/lymphedemainthenews for additonaly information about Lymphedema, as well as other events/call to actions happening, especially in Texas.
If you wish to share your story, please submit your request at http://goo.gl/forms/rqo8jg28j1
Sponsors and Co-Sponsors of the Lymphedema Treatment Bill ---
Tiffany Howe was born with Primary Congenital Lymphedema (Milroy’s Disease). After 27 years of struggling with this ailment, she was given a choice of losing her left leg or undergoing the Charles Debulking procedure. The choice was difficult and very challenging to make. She chose the Charles Debulking procedure and could not have guessed the life-changing experiences which would result. Full recovery took a year and included her learning to walk again. For the next five years, Tiffany used her training as a Registered Nurse to research and study any available information about Lymphedema. Research ultimately led me to the conclusion that Lymphedema patients are in need of support for this currently incurable disease. Support includes education and advocacy. I represent Virginia as part of the Lymphedema Advocacy Group, which is a patient-centered group, raising awareness. Our mission is to get passage in Congress for the Lymphedema Treatment Act.
Come hear her story and more!
For more information, too, please refer to the Lymphedema In The News fb page (http://facebook.com/LymphedemaInTheNews).
Dr. Stanley Rockson (of Stanford University Medical School) states that: "Lymphedema is a common disease. Approximately 10 million Americans, for example, have lymphedema secondary to breast and pelvic cancer therapy, recurrent infections, injuries, or vascular surgery." (2010) Imagine, if there were approximately 10 million Americans then, how many more there are now in 2014 (knowing that there is no cure for it as it stands to date)?
For many years, I had key advocates come on my show to discuss various cases and, especially, the aspects of advocating in the legislature. On January 27th, Heather Ferguson (one of those advocates) will come on my show to discuss some updates on those legislative issues being presented.
Today, though, I will open the mic up to patients, advocates, and caregivers especially to tell their stories on how Lymphedema has affected them. We will then share this with legislators to personally hear the many stories typical to illustrate the pervasiveness of this condition.
Please mark your calendars and join us on March 6th at 10a CST to share and/or be better informed about these issues.
Come hear Heather Ferguson provide us with some updates about THE LYMPHEDEMA TREATEMENT ACT via my radio show called BEYOND WORDS LIVE. She'll provide the latest and greatest on what is happening with the Hill on our Bill. Invite all your State Advocates to attend, all Lymphedema patients to attend, your LE physical therapist to attend, as well. We need all the voices that we can get!
For a little insight, Heather passed an email out on January 15th which included this announcement -- LYMPHEDEMA TREATEMENT BILL is now up! She writes "All our hard work and preparation over this past year has come to fruition today! This morning the Lymphedema Treatment Act was introduced into the 113th Congress (bill number HR 3877) by our lead sponsor, Rep. Reichert (R-WA), and co-leads Rep. Lance (R-NJ), Rep. Blumenauer (D-OR), and Rep. Braley (D-IA)."
For more discussions about these issues go to Lympedema In the News on facebook - http://facebook.com/LymphedemaInTheNews - or, see the website - http://www.capwiz.com/lymphedematreatmentact/home/. See also this article - http://reichert.house.gov/press-release/reichert-introduces-critical-legislation-improve-healthcare-lymphedema-patients
Well, the actual awareness day is actually on March 6th; however, the usual show is on Saturdays so we keep with a part of tradition to take a break from domestic violence issues to talk about lymphedema and advocacy for lymphedema patients everywhere, with a special focus on what is happening in the United States with HR 4662 making its way in the houses. Today, we will revisit the issue with as many of the same panel from last year to discuss these and related things to the needs of the lymphedema patient. Many on the panel have lymphedem themselves or have been/or are closely related to someone that is going through this condition that simply doesn't have a cure as of yet, albeit we all remain faithful in that some day we will see skinny limbs and things after they determine what exactly works to de-block the lymphatic system in our bodies.
October 23, 2012: October is National Physical Therapy Month and National Breast Cancer Awareness Month. Although many consumers might not think of physical therapy and breast cancer treatment being related, in this interview Nicole Stout, PT, MPT, CLT-LANA, describes why physical therapy is so important in a breast cancer treatment plan, not just eventually but early on. She also outlines the relationship between breast cancer and lymphedema and provides advice for those who might be at risk.
Subscribe to Move Forward Radio podcasts on iTunes.
To learn more about physical therapy, visit MoveForwardPT.com.
Pelvic floor health is certainly not something women talk about during happy hour or over lunch. Occasional giggly references to ‘don’t make me laugh (I’ll pee!)’ or kegel exercises is about all that takes place when talking about this important aspect of a woman’s health.
However, the fact that this conversation can be awkward shouldn’t diminish its importance. Do you realize that in addition to controlling our urine, helping us to have babies, our pelvic floor also holds up our guts? There is much to learn about having a healthy pelvic floor – what it is and how to care for it. Join us to hear more.
ABOUT PLAID FOR WOMEN:
Plaid for Women radio is produced to give you information, advice and resources to be YOUR wise advisor. Our goal is to help you achieve your goals, gain influence, and be heard.
Every show, we are committed to bringing you new ideas and offering new ways of thinking to give you opportunities to change your thinking and change your life. You CAN live the life you've imagined!
LET’S GET SOCIAL!
CONNECT WITH TODAY’S GUEST:
Rebecca Lucas-Gregg, Marketing Manager
www.unthealth.org | www.unthsc.edu
Join Dr. Weizer in this re-airing of this great show as he discusses Occupational Therapy in oncology with Amy Kay. Amy is an Occupational Therapist that has been serving cancer patients for 13 years. Amy explains the role of occupational therapy in oncology is “to facilitate and enable an individual patient to achieve maximum functional performance, both physically and psychologically, in everyday living skills”. Dr. Weizer and Amy also discuss the role an OT plays in the mind, body and heart along with the needs of the physical body.
Kevin A. Baptists, was born in Boston, Mass. His family is from Trinidad and Tobago. he went to St. Peter Marian and went to ITS TECH for computer aided design. He is 37 year's old. He is a farmer and speaker. He also is an advocate for lymphedema. he was born with it. Lymphedema is the swelling of body limbs due to a blockage in the lymphatic system or due loss of lymph nodes due to surgery or drama.
ThruOurEyes - 8-9pm LIVE! Joe will interview Sharla Glass, industry relations, and Amanda Tolson, pharmacy relations, from EnVision America. Highlighting EnVision America's history, best practices for labeling prescriptions, methods to obtain labeling at local pharmacies, and the next steps to have labeling for the blind
IBC Fact And Fallacies - 9-10pm LIVE! Josh Levin from LympheDIVAs will discuss lymphedema and show us medically correct and fashionable compression apparel for the savvy and stylish breast cancer survivor which will inspire her to feel beautiful, strong, and confident.
Join Host Live Chats
- High Frequency Radio Network (25 chatters)
- Ebony Empress (8 chatters)
- New Way Power Hour (7 chatters)
- TheThinkingAtheist (7 chatters)
- Bellesprit (6 chatters)
- NLPI RADIO USA KURT LOGSDON (5 chatters)
- Radio Jihad Network (5 chatters)
- The Hereafter Is Now Network (4 chatters)
- Chef Cardinale Cooking Show (3 chatters)
- TLO Ministry (3 chatters)
- USA Emergency Broadcasting Network (3 chatters)
- WC A Woman with CP (2 chatters)
- JASmius (2 chatters)
- Sandra Booker (2 chatters)
- Journey Into Light (2 chatters)
- KimberleyJ (1 chatters)
- Lori Mitchell (1 chatters)
- Nu Power Radio Network (1 chatters)
- SPECULATION SPORTS (1 chatters)
- Jay King Network (1 chatters)
- Empowered By Christ (1 chatters)
- dijones247 (1 chatters)
- DivaTalkRadio (1 chatters)
- Broad Street Line (1 chatters)
- We are TOPS (1 chatters)
- TheLegacyOfANation (0 chatters)