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Join us as we speak with Senator Jeff Sessions (R-AL) about S.Res. 414: A resolution designating April 2014 as “National Congenital Diaphragmatic Hernia Awareness Month”
Submit your questions for Sen. Sessions at email@example.com
In this episode I will discuss the economy of the USA. Inflation is escalating. Shortage in food banks. School lunches have been cut in portion. Children are still hungry after lunch. Go look at the size and portion of the lunches that are being given to our children. They come home starving. It has nothing to do with children and teens being overweight but it was an excuse that Michelle Obama used. The problem with overweight children is that they eat fast food. Sometimes, it is all some parents can afford. GMOs in our food are taking away the nutrition and only those who have money can truly afford to buy organic foods.
Current news - Medicare cuts starting in March 2015 will cut physician's payment by 21%. That means that the cost will be charged to the patient. It doesn't matter if one has supplemental insurance because these insurance companies only pay 20% of the difference of Medicare.
Doctors will get paid for telling patients of end of life options. Doctors will also get paid for reporting patients' health records to the government's panel.
I do see Medicare eventually going bankrupt and vouchers would have been a better solution.
As for younger people they are having a harder time than seniors in obtaining health care services. The reason being is because of the high deductible under Obama care. I know someone who needs surgery for a hernia and they can't even be seen until they pay the doctor $300.+. Going to the ER only stabilizes the patient at that time and then they must follow up on their own.
If you want a private reading I can be reached at http://www.Kasamba.com/psychic/mia0899cs
Love and Light,
This is a message from Anna Jaworski, host of "Heart to Heart with Anna," detailing where Listeners can send tax deductible donations so "Heart to Heart with Anna" can continue ("Heart to Heart with Anna," 3910 Sierra Blanca Blvd., Temple, TX 76502) and letting Listeners know that regular programming will begin again on January 27, 2015. The theme for Season Four is "Tales from the Trenches" and is already shaping up to be quite a lively and interesting season.
If you are interested in being on the show, please write to Anna by filling out the form on the website www.hearttoheartwithanna.com. The form is available under the Be On The Show tab.
We look forward to bringing you Season Four of "Heart to Heart with Anna" beginning January 27, 2015.
When a person is born with a broken heart, parents must face a multitude of decisions -- many life-threatening and terrifying. As children age, they themselves become aware of their heart problems and face their own mortality. Many of us in the heart defect community (CHD) have faced the death of loved ones or friends. How does being a member of the CHD community take a toll on its members? What are some ways we can deal with the trauma that we must face? One way is through art therapy or music therapy. Today's show will deal with this topic and will feature Angela Loehr, the founder of HeartWire, International (http://heartwiremyheart.org) and Megan Tones.
What kills 1000 people a day or one person every two minutes? What kills more people annually than breast cancer, lung cancer and HIV/AIDs combined? What is one event that kills most of the people who suffer from it, but who could possibly be saved? The answer is sudden cardiac arrest (SCA).
Today's show will be about the survivor of, not one but over 140 sudden cardiac arrests, and his wife. We'll learn why he has suffered so many SCAs, even though he is a relatively young, otherwise healthy man. Lastly, we'll find out what his experience has taught him and his family and what he and his wife have established so others, like he, will be survivors.
The most common cyanotic congenital heart defect that presents in the first month after birth is transposition of the great arteries (TGA). There are two major forms of TGA -- dextro-TGA (d-TGA) and levo-TGA (l-TGA) or congenitally corrected TGA (also known as cc-TGA). Because cc-TGA is rarer than d-TGA, it's not often spoken about. On this show we'll have two adult survivors of cc-TGA talk about what it's like living with cc-TGA, how it's affected their lives and what advice they have for parents of cc-TGA and for adult survivors of cc-TGA.
Is it safe to use nontraditional medicine with babies and children who were born with congenital heart defects? Do others in the heart community use nontraditional medicine? Why would a parent consider using complementary and alternative medicine with their children born with heart defects?
Today's show will feature Carolyn Harrington, the owner of Maty's Healthy Products. Carolyn is the mother of Maty, a daughter who was born with a congenital heart defect and who has had several open-heart surgeries. Discover why Carolyn started Maty's Healthy Products and whether or not using complementary and alternative medicine might be an option for you or a loved one.
The information contained in our show is not intended to-constitute comprehensive professional medical services or treatment of any kind. The CONTENT SHOULD NOT BE USED FOR MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT. Our show should be considered as an educational service only.
in Self Help
Susun Weed answers 90 minutes of herbal health questions followed by a 30 minute interview with Mitzi Weinman.
Mitzi Weinman is the founder of TimeFinder, which offers practical approaches to personal productivity. As a coach, workshop leader, and professional speaker, she helps people develop good habits and techniques to reduce stress which can result from not planning, procrastinating, feeling disorganized, and overwhelmed, and rushing to get things done, at work and/or at home. Since 1989, TimeFinder’s programs have provided ongoing support and professional and personal development to hundreds of companies, individuals and associations including New Balance, Reebok, Boston Symphony Orchestra, Dana Farber Cancer Institute, Pearson Education and Marriott University. She earned a bachelor’s degree from the Newhouse School of Communications at Syracuse University and lives in Needham, Massachusetts, with her husband, son and dog.
this episode Q&A- includes:
• PCOS- treatment to achieve fertility..
• cysts? consider dissolving herbs such as red clover or comfrey..
• varicose veins- witch hazel, plantain oil, fenugreek, horse chestnut and avoid spicey foods
• how to make hawthorne tincture..
• Clostridium difficile colitis- slippery elm balls and corn silk infusions..
• why Susun does not use golden seal.
• preventing premature rupture of membranes (PPROM)..
• yarrow for mouth care..
• hiatus hernia- explanation and recommendations..
• marijuana is a magnifier..
How can members of the congenital heart defect (CHD) community lobby for change in today's laws in the United States? One thing they can do is to come together as a unified group to speak to their lawmakers and request, in a collective voice, for changes to occur.
This is how the Congenital Heart Futures Act came into effect. Members of the Adult Congenital Heart Association (ACHA) organized a coalition of members to storm the Hill together to request more government money being spent on those with congenital heart defects. Today's episode will feature 2 ACHA members who met with lawmakers on the Hill to discuss the future of those born with congenital heart defects.
If you've ever wondered how you could take a stand a make a difference, not only for today's survivors but for all future survivors, you won't want to miss this show.
Have you ever wondered what Eisenmenger's Syndrome is? Who gets it? What are the symptoms? How does it affect a person's body from childhood to adulthood? What changes occur with the aging survivor?
Carolyn Robinson, a long-time Eisenmenger Syndrome Survivor will answer these questions and more as she details her life story of being diagnosed with this condition and surviving long enough to become a grandmother! Carolyn is a published author. She wrote an essay entitled "Leading the Troops" for The Heart of a Mother, which was an anthology of stories by women affected by congenital heart defects. Carolyn's essay was in the Mothers with Congenital Heart Defects chapter and detailed her efforts to become a mother.
As the parent of a child with a life-threatening heart defect, it's easy to feel overwhelmed by the new "heart world" the family is immediately part of. On this show two mothers who have children with critical congenital heart defects (CHDs) will discuss how they became empowered members of the CHD community by tapping into ways to help others in their community.
Wayverly Mouse-Evangelista will share how her love of arts and crafts enabled her to find a way to reach out to others in the CHD community. She will share what specific items she has created for the heart community and how others can find them.
Susan Vanderpool will share how her situation caused her to see a need for vital information in a heartbeat. She will tell us about how she created a product to calm mothers' fears. Having a school-aged child with a major heart defect in school full-time, away from a loving parent, can be a scary prospect. Ms. Vanderpool shares how her product can relieve parents' anxiety about this situation.
We will also hear from CHD Survivor Natalie McGee how she found a way to give back to her community. Through her own adversity she was able to create a product to help herself and others. Find out what she created and how you can benefit from the creations she and her mother have designed.
Sometimes reaching out to others in need is the best therapy a person can have!
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