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Jeni Treehugger Patient Expert

US
Some of my biggest passions in life are cooking, eating and being vegan. I enjoy sharing with people what exactly is involved with living a vegan lifestyle. It's not complicated, it's not hard, it's not boring and I hope all this is reflected in my blog. I'm no-one special but I do live a remarkably special life. GO VEGAN!
Communities: Vegan

ERIN HAYES

US
I'm a mother of two who recently lost our first child, Charlotte, to a rare chromosomal issue that resulted in various health issues and complications. She was 3 years and eight months old. With her we dealt with developmental issues as well as heart, lung, kidney, and feeding issues. She used oxygen and a feeding tube for most of her life. Ella, my second child, is not affected by this...

Terri People's HealthBlogger Award Nominee

Burlington, Iowa
Ava~Hope for Congenital Diaphragmatic Hernia. I am passionate about teaching parents how to advocate for their child's health. My third daughter Ava was born with Congenital Diaphragmatic Hernia. CDH is when (inside of the womb) the diaphragm does not form properly. The abdominal organs move up into the chest cavity, compromising the heart and lungs. Half of all babies born with this birth...

Amy

allegany, New York
To all my ladies that are reading this because they have been diagnosed or told they have some type of Vulvodynia please don't freak out.... There are many reasons as to why women start experiencing Vulvodynia. Let me first start by saying Vulvodynia is NOT a diagnosis it is a symptom. Vulvodynia means Vulvar pain.. The diagnosis is the more complicated part. Dealing with Vulvodynia is...

Tina

US
I am a stay at home mom of two beautiful girls. I have a background as a Physical Therapist Assistant, but stopped working to stay at home with my girls after my youngest was born. Since then, I've been living in the world of congenital heart defects after my youngest daughter was diagnosed with Tetralogy of Fallot with Pulmonary Atresia, with several other complications. Its not been an easy...
Communities: Children's Health

Holli

Beaumont, Texas
I am mommy to one son, Austin, who was diagnosed with a catastrophic form of epilepsy known as Infantile Spasms/West Syndrome at six months old. He was diagnosed in May 2008, and it has been an uphill battle ever since. We struggle with numerous daily seizures and developmental delay. My blog tracks our progress (medically and emotionally) as we continue to fight for relief from his...
Communities: Epilepsy & Seizures

Catrina Johnson People's HealthBlogger Award Nominee

Pike County, Kentucky
My name is Catrina, I am a stay at home mom to 3 children. My days consist of taking care of my children, but online where everyone has the ability to connect and share information I have the obligation to spread the word of a rare disorder called Hirschsprungs Disease. My son who is now 3 has struggled with this rare disorder of the intestines since he was born. I am here to educate anyone who...

MedicalMalpracticeCarbondale

Carbondale, Illinois
Medical Malpractice Carbondale IL Alleman & Hicks Attorneys At Law, is conveniently located in Carbondale, IL, we are an experienced law firm dedicated to helping individuals and companies resolve their legal problems in a wide variety of contexts, including personal injury, bankruptcy, family law, litigation, employment, and general practice.Representing victims of Medical Malpractice due...

P.Allen Jones

US
P.Allen Jones is a writer living in the U.S. She is a patient and advocate who speaks about living with Sickle Cell Disease (SCD). SCD affects millions of people all over the world. In the US, sickle cell disease was thought to affect only African-American's. Today, this is no longer true. With people migrating and mixed races, SCD appears in people who don't look "african." This blood...

Christine from WI Patient Expert

Green Bay, Wisconsin
About 5 years ago I started having headaches when I would lie down that mysteriously dissapeared when I sat up. An MRI determined I had a neurological disorder called a Chiari Malformation. I tried many different prescription medications that did nothing for my pain before I was referred to a neurosurgeon. Two surgeries later I ended up experiencing the worst pain imaginable, wondering if I was...
Communities: Chiari Malformation