As a followup to his previous best-selling book, Issues and Management of Joint Hypermobility: A Guide for the Ehlers-Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome, Dr. Tinkle has created this handbook with several contributors to expand insights into the understanding and management of Ehlers-Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome. Dr. Tinkle has received many accolades for his ability to take a complex condition and make it understandable in everyday language: ...provides a wealth of information about the natural history, and physical and medical management... It should be of great value to patients. - The American Journal of Medical Genetics Reader comments... ...a useful tool in helping me obtain the type of care I need to manage my disorder... This book is simple but not oversimplified. It is an excellent basic resource, giving a clear, concise, and useful overview for those (like myself) who live with hypermobility. Super book for EDS! Finally a book that everyone can understand. ...thoroughly explores the problems associated with EDS-HM. It is a relief to realize that it is not just me... ...a tremendous service for the health care community and the families and friends of those diagnosed or not yet formally diagnosed folks with EDS-HM... joy and clarity in reading the very 'easy to read' text chapters detailing out the impact of EDS-HM... In addition to the weatlth of positive reviews, Dr. Tinkle's previous book on the same subject was a best seller in several categories: - Genetics - Medical Genetics - Orthopedics - Family and General Practice Brad T. Tinkle, M.D., Ph.D., is a clinical and clinical molecular geneticist at Cincinnati Children's Hospital Medical Center (CCHMC). He specializes in caring for individuals with heritable connective tissue disorders such as Ehlers-Danlos syndromes, Marfan syndrome, osteogenesis imperfecta, and achondroplasia among the many.

Kevin Muldowney, MsPT has been treating people with Ehlers-Danlos Syndrome since 2005. As a physical therapist, he has developed an exercise protocol to help stabilized the many joint subluxations/dislocations associated with this genetic disorder. This book is intended for the person diagnosed with EDS to both inform them about the healthcare team needed to properly treat them as well as to guide both the physical therapist and their patient with EDS through the Muldowney exercise protocol. This book will cover such topics as: how joints sublux in this population, how to find the right physical therapist, how to exercise without injury and what physical therapy techniques works best. By the end of this protocol people with EDS should be better informed about what is going on with their body and how to make it better.

My niece was 36, newly married, and on top of the world, when she collapsed and died. Her autopsy report caused us to panic--there was something in our blood that could trigger sudden death. As a mother, I prayed for the curse to spare my children. As a geneticist, I plotted to find the killer. Without planning to do so, I became a medical detective.
The book tells of the sorrows a mutation caused my family for generations, revealing a history of resilience and hope. As the stories unfold, I weave in discussions about genetic testing, screening, and gene therapy. The aim is to raise awareness of the crucial role of genetic testing in safeguarding personal health and patient care. I believe I became a geneticist at a time when few women pursued this path because I was destined to help understand the family illness and advocate for genetic testing.
Experts agree on the value of genetic testing when there is a family history of disease, or if the patient has an illness frequently caused by a mutation. Knowing the disease mutation lets other family members find out if they have it too and need preventive care. The book explains that doctors can order tests with genetic counseling at relatively low cost and how this will help them prescribe preventive actions, make earlier diagnoses, and get better outcomes. The book's genetic discussions also delve into the implications of broad-based genetic screening without a family history. Policymakers are currently considering the benefits and drawbacks of this approach and I present both sides of this debate.
While working on this book I uncovered a family secret hidden for over one hundred years. Family lore had it that a heavy dressmaker's mirror fell on and killed my uncle when he was four. But the death certificate told a different story. The true cause of my uncle's death was heart failure. My grandparents fabricated the dressmaker's mirror accident to protect their surviving children's marriage prospects. Long before the discovery of DNA, my grandparents intuited and feared James Watson's message, We used to think that our fate was in our stars, but now we know that, in large measure, our fate is in our genes. The book suggests genetic testing and associated medical intervention can yet change our fates.

Your mind and body are inextricably linked. Ignore your inner voice, and your body will pay the price. Ingrid Fredriksson's groundbreaking research on the link between consciousness and epigenetics was met with acclaim at a scientific conference in Tucson. Academics and independent researchers alike agreed: 'This must be shared with the world!' This book is your chance to learn more. Explore the invisible forces that shape our lives, delving into the world of epigenetics and how our genes are activated or silenced by everything from cell type and disease to physiological and psychological stimuli. This book pays special attention to the impact of emotions on health, exploring how trauma, stress, and negativity affect our well-being at the cellular level. Discover how cultivating positivity can lead to a longer, happier life. Fredriksson's groundbreaking study - likely the first of its kind - reveals the practical, everyday implications of epigenetics, demonstrating how our consciousness and emotions influence our health and well-being. This is essential knowledge for everyone, especially healthcare professionals.

Andy's book will provide hope for those who so desperately need it. These stories of strength and determination are inspiration to keep fighting in our own lives.

--Celine Dion

These are tales of warriors who have beaten the odds by making their dreams come true. These are stories that will give you hope. And by buying this book, you will bring us closer to a cure. That is my dream.

--Lewis Black

After spending time with cystic fibrosis warriors throughout the country, I've quickly realized they are the toughest and most resilient people I have ever met. The outlook CF warriors have on life is one that everyone should strive to have.

--Colton Underwood

These are the stories of CF warriors who refused to succumb to a distressful prognosis, and instead thrived through the power of belief.

--Megan Fox

How to Deal - and Heal - for those with Rare Chronic Illness like EDS

Tired of being told there's no name or treatment for your illness?

That it's all in your head or that your pain can't be real because you're too young/old/pretty/bright/healthy/normal to have a chronic disorder?

What if instead there was someone who knew what you were going through and could teach you strategies for coping with rare chronic illness?

This is not a false hope. You can turn pain into possibility with this life-changing book that can help everyone with elusive hypermobile Ehlers Danlos Syndrome (hEDS) - from those newly diagnosed to those who have suffered in silence for decades. Wherever you are on your journey navigating the complexities of chronic illness, you're not alone.

In Holding It All Together When You're Hypermobile, Christie Cox explores not only the physical effects of hEDS but its emotional impact as well. As a fellow patient and medical rarity, known to doctors as zebras, she's experienced her body's betrayal and suffered through the myriad complications stemming from this disease. But she's also found a way out from the depths of this life-altering disorder with wisdom you can turn into hope.

As a self-advocacy guide, she offers practical, no-nonsense advice about living with chronic illness and the concrete steps you can take to achieve a new normal. In her book, you'll discover...

• A healing prescription for the miracle of the modern mindset

• A look at the latest scientific research on the edge of answers

• Q&A interviews with expert doctors and advocacy groups

• Guidance for how to help loved ones better understand hEDS

• Christie's own inspiring story of how she came to live her best life

• Lessons, questions and quotes to inspire your search for answers

Holding It All Together When You're Hypermobile gives you the tools and resources you need to get back to living the life you want. Reading it will not only boost your confidence but empower you to change your life for the better.

To learn more about Christie's book, visit www.holdingitalltogether.com

If you want to learn more about Christie's advocacy work, visit www.journey2joyous.com

Please note: This is the same book with the same information that was in the original release of the Joint Hypermobility Handbook. This version has an increased size so as to allow for larger margins - convenient for notetaking while ingesting the information

Book content description:

As a follow-up to his previous best-selling book, Issues and Management of Joint Hypermobility: A Guide for the Ehlers-Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome, Dr. Tinkle has created this handbook with several contributors to expand insights into the understanding and management of Ehlers-Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome. Dr. Tinkle has received many accolades for his ability to take a complex condition and make it understandable in everyday language: ...provides a wealth of information about the natural history, and physical and medical management... It should be of great value to patients. - The American Journal of Medical Genetics Reader comments... ...a useful tool in helping me obtain the type of care I need to manage my disorder... This book is simple but not oversimplified. It is an excellent basic resource, giving a clear, concise, and useful overview for those (like myself) who live with hypermobility. Super book for EDS Finally a book that everyone can understand. ...thoroughly explores the problems associated with EDS-HM. It is a relief to realize that it is not just me... ...a tremendous service for the health care community and the families and friends of those diagnosed or not yet formally diagnosed folks with EDS-HM... joy and clarity in reading the very 'easy to read' text chapters detailing out the impact of EDS-HM... In addition to the wealth of positive reviews, Dr. Tinkle's previous book on the same subject was a best seller in several categories: - Genetics - Medical Genetics - Orthopedics - Family and General Practice.

Brad T. Tinkle, M.D., Ph.D., is a clinical geneticist at Peyton Manning Children's Hospital. He specializes in caring for individuals with heritable connective tissue disorders such as Ehlers-Danlos syndromes, Marfan syndrome, osteogenesis imperfecta, and skeletal dysplasias among the many.

Embark on a journey of empowerment and resilience with The Charcot Marie Tooth Disease Mastery Bible: Your Blueprint for Complete Charcot Marie Tooth Disease Management. This comprehensive guide begins with a historical exploration of CMT, delving into its classifications, genetic underpinnings, and symptomatology. Gain insights into the diagnostic process, debunk myths, and understand the progression of CMT.

Navigate the intricate landscape of medical management, from orthopedic interventions and neurological care to pain management strategies. Uncover holistic and alternative approaches, incorporating nutritional strategies, herbal supplements, and the mind-body connection into your care plan. Explore exercise and movement therapies, stress reduction techniques, and the principles of integrative medicine for a comprehensive approach to CMT management.

Learn to adapt daily life with CMT, making home modifications for safety, utilizing adaptive tools and technology, and addressing mobility and transportation challenges. Tackle career and employment considerations, foster social interactions and relationships, and prioritize emotional and mental well-being. Discover coping mechanisms, build resilience, and engage with support systems and communities.

Prepare for advanced care planning, understanding the nuances of advanced CMT, and addressing legal and financial planning. Explore healthcare directives, caregiver support and training, and end-of-life considerations, including palliative care options and transitioning to assisted living. The Charcot Marie Tooth Disease Mastery Bible is a beacon of guidance, offering a holistic blueprint for managing every aspect of life with CMT with grace and strength.

Tried everything but still not feeling better?

If your depression keeps coming back or is even getting worse, then you may be suffering from bipolar II or soft bipolar disorder. Commonly misdiagnosed, these mood disorders are characterized by recurring bouts of depression along with anxiety, irritability, mood swings, sleep problems, or intrusive thoughts.

Why Am I Still Depressed? shows you how to identify if you have a nonmanic form of bipolar disorder and how to work with your doctor to safely and effectively treat it.

Author James R. Phelps, M.D., gives you the latest tools and knowledge so you can:

• Understand the Mood Spectrum, a powerful new tool for diagnosis
• Know all your treatment options, including mood-stabilizing medications and research-tested psychotherapies
• Examine the potential hazards of taking antidepressant medications
• Manage your condition with exercise and lifestyle changes
• Help family and friends with this condition understand their diagnosis and find treatment

A Dietitian-Approved, Customizable Food Plan to Combat Iron Overload

Also known as iron overload or bronze diabetes, hemochromatosis is one of the most common genetic disorders in the US. With no known cure and life-sapping symptoms, such as fatigue, joint pain, heart abnormalities, and skin discoloration, it can lead to very serious medical conditions and is without question a life-altering diagnosis.

Living Well with Hemochromatosis is a friendly guide to taming your symptoms by taking total control of your diet. It offers an easy-to-understand overview of micronutrients, tips and tricks for identifying high-iron foods and limiting absorption, stories from others living with hemochromatosis, and simple and delicious recipes.

From carnivores to vegans, this book offers something for all lifestyles. Recipes span from salads, side dishes, entrees, and smoothies, each with nutritional analysis.

Unlock the secrets to effective Amyloidosis management with The Amyloidosis Mastery Bible: Your Blueprint for Complete Amyloidosis Management. In this comprehensive guide, delve into the intricacies of Amyloidosis, exploring its types, symptoms, and risk factors. Discover the significance of early detection and unravel the myths surrounding the condition. Navigate the medical landscape with insights into medication protocols, therapeutic procedures, and the latest in clinical trials. The diagnostic journey comes alive as you explore laboratory tests, imaging techniques, and genetic screening.

Embark on a holistic approach to wellness with detailed sections on diet, nutrition, and essential nutrients tailored for Amyloidosis patients. Uncover the power of stress reduction techniques, herbal remedies, and the mind-body connection. Engage in safe and effective exercise routines designed for Amyloidosis patients, supported by physiotherapy insights. Foster mental health and resilience through mindfulness, meditation, and positive thinking. Navigating the healthcare system becomes second nature with tips on insurance, medical appointments, and community resources.

This book extends beyond medical aspects, offering guidance on socializing, managing isolation, and maintaining a balanced social life. Financial planning, employment rights, and long-term care considerations are addressed, ensuring a comprehensive approach to living with Amyloidosis. Stay informed about the latest research advancements, cutting-edge treatments, and global efforts in Amyloidosis awareness.

Discover lifestyle modifications for an Amyloidosis-friendly home, workplace adjustments, and travel tips. Explore healthy sleep habits, stress management, and time productivity. Embrace nutrient-packed meals, anti-inflammatory foods, and meal prepping strategies. Access a wealth of resources for further reading, trusted publications, online support groups, educational videos, and disease management tools.

The Amyloidosis Mastery Bible is your indispensable companion, equipping you with knowledge, strategies, and resources for a holistic journey towards Amyloidosis mastery.

Have you been struggling with health issues for years and recently diagnosed with MTHFR gene mutation? You've identified the cause of your health issues, but now unsure what to do next? Dr. Terranella has treated hundreds of people with MTHFR gene mutations and now has released a comprehensive guide to help you navigate MTHFR treatment. Go beyond just learning about MTHFR gene mutation and actually address your individual treatment options. Rather than a one size fits all protocol, Dr. Terranella provides you with the why behind the what to do. You will learn what to expect and what to do when things do not go as planned. Dr. Terranella is the best doctor I've ever seen! If you want to understand MTHFR, he is THE guy to listen to! I have a level of understanding I never thought possible, and better than that, I have real results from treatment Mike Hardenbrook, Patient

It's All Relative: One Family's Story of Kidney Disease follows the journey of my family members and our history of Polycystic Kidney Disease (PKD). The stories we share demonstrate how PKD affects us differently, physically, emotionally, and in all other aspects of our lives. While technical information about the disease is available, there's less about how people feel and cope with the symptoms. This story is about the similarities and differences in our experiences with PKD. Writing these stories has been cathartic for our family, and we hope that by sharing our story, we can support others in their journey with Polycystic Kidney Disease.

In his mid fifties, Helmut Schroeder was diagnosed with Beh et's Disease BD], a rare autoimmune disorder that causes blood vessel inflammation throughout the body. This disease is painfully disabling and potentially fatal. Beh et's Disease is not contagious and is classified as a Chronic Disease, which is a condition lasting three months or longer, by the definition of the U.S. National Center of Health Statistics. Schroeder's physicians told him there is no cure for this disease and recommended managing it with drugs as the only option available. So he went on those drug treatments for a period of time and had severe allergic reactions from them. Not only did his health not improve - it actually worsened, progressively. Yet, his physicians offered no other treatment options. The other alternative was a diet change; but, his physicians did not support that idea. At that point, he realized that he had to find his own answers for his health issues. He eased out of the drug treatments and stopped eating the Standard American Diet SAD]. He began his new diet of mainly white rice with selective plant-based whole foods. This kind of diet is recommended by a group of physicians who practice Lifestyle Medicine. With his positive attitude, he researched and found out about most of the foods that aggravate his BD. Almost thirty years later, he is still in good health, maintains an active lifestyle, and remains nearly BD free. This is his story. In this book, he describes the trials and errors he encountered. He also describes how he learned to avoid most of the allergy-causing foods that aggravate his BD, and how he restored his health. With his life-affirming attitude, he shows you how to become healthier and more positive, as well as challenge yourself to change.

Written by Cai Stoudemire and Richon Badger. Illustrated by Barderies Hampton. This book is written from Cai's point of view and has wonderfully detailed pictures for children and literature for adults. Cai's ABC's of Sickle Cell is a very fun and needed resource for the community at large to know and understand more about Sickle Cell. All while giving a glimpse of what patients with Sickle Cell experience. Cai encourages the readers in the normal @CaiStrong_ fashion and continues to be a light for the Sickle Cell cause.

WHAT IS EPIGENETICS? Epigenetics is an emerging field of science that studies alterations in gene expression caused by factors other than changes in the DNA sequence. Epigenetics: The Death of the Genetic Theory of Disease Transmission is the result of decades of research and its findings that could be as critical to our understanding of human health as Pasteur's research in bacteriology. Dr. Joel Doc Wallach has dedicated his life work to identifying connections between certain nutritional deficiencies and a range of maladies, formerly thought to be hereditary, including Cystic Fibrosis and Muscular Dystrophy. This nexus between nutrition and so-called genetic disease has been observed in both humans and primates, and it is the central theme of Epigenetics. To bring us Epigenetics, Wallach has teamed with noted scholars Dr. Ma Lan and Dr. Gerhard N. Schrauzer. Their collective expertise gives this book its far reaching perspective. Epigenetics is of vital importance to anyone who wants real knowledge about how the human body functions, and it provides a path for better health. Epigentics dispels the dogma and misinformation propagated by medical institutions and doctors resistant to change. Epigenetics is the beginning of a new era of well-being on this planet.

The Cystic Fibrosis Mastery Bible: Your Blueprint for Complete Cystic Fibrosis Management is a comprehensive guide designed to empower individuals and families affected by cystic fibrosis (CF). Beginning with an exploration of the fundamentals, including the genetics of CF and symptom recognition, the book provides a deep dive into medical management strategies. From pharmacological therapies and pulmonary care to nutritional support and infection control, each chapter offers valuable insights and actionable advice. Patient stories offer a personal perspective, enhancing understanding and fostering a sense of community. The guide also delves into emerging treatments, holistic and alternative approaches, emphasizing the role of exercise, breathing techniques, and nutritional needs unique to CF. Addressing mental health, coping mechanisms, and navigating relationships, the book provides a holistic approach to CF management. Looking towards the future, it explores promising avenues such as gene therapy, personalized medicine, and global CF care initiatives. With a vision for advocacy and awareness, this book is not just a guide-it's a source of hope and empowerment for those navigating the complex journey of living with and managing cystic fibrosis.

The Duchenne Muscular Dystrophy Mastery Bible: Your Blueprint for Complete Duchenne Muscular Dystrophy Management is a comprehensive guide offering support, insights, and a roadmap for individuals and families navigating the challenges of Duchenne Muscular Dystrophy (DMD). Delve into the genetic puzzle of DMD, understanding dystrophin, and recognizing early signs. Learn about medical management, including corticosteroid therapies, cardiac care, and respiratory support, as well as physical and occupational therapy approaches. Explore holistic perspectives with integrative medicine, acupuncture, herbal supplements, and mind-body practices. The book provides practical guidance for daily life, covering adaptive equipment, home modifications, education, and social inclusion. Address psychological and emotional wellness with coping strategies, mental health support, and resilience-building techniques. Empower yourself through creating a personalized DMD management plan, collaborating with healthcare providers, and incorporating holistic approaches. Advocacy and empowerment sections guide you in understanding your rights, navigating healthcare systems, and participating in research and trials. Explore the science of hope with breakthroughs in gene therapy, stem cell research, advances in muscle biology, and innovative drug discoveries. Understand the role of patient advocacy in research and the impact of technology on DMD. This book is a beacon of knowledge, support, and hope for anyone affected by DMD.

If you are dealing with Lyme disease or know someone who has it, you might be wondering if making changes to your diet can have any impact on your recovery. Well, it's no news that people with certain illnesses often have to switch to a specific diet in an attempt to manage the condition or support their recovery. This is no different with Lyme disease.

Lyme disease is linked to chronic inflammation. When you're in this state, the last thing you want to do is make poor dietary choices as this is like fueling a burning fire. It will only get worse!

The good news is that following a proper diet can help ease the symptoms of Lyme disease and support your healing process while improving your overall health. That is the whole idea behind Dr Barbara's Alkaline Diet Guide.

The book is written to guide you on how to follow Dr Barbara plant-based way of eating to relieve symptoms of Lyme and reverse it over time.

Everyone living with EDS should have a copy of this manual. Open it up, and discover the path to relief and empowerment you've been looking for.

Living with Ehlers-Danlos Syndrome (EDS), particularly the hypermobility type, presents unique challenges that can significantly impact your daily life. However, there is hope and practical guidance available. The strategies and insights offered in this book can be a game changer for you.

In my practice, I've seen first-hand how the right approach can make a world of difference for those living with EDS. This book provides practical, evidence-based methods for managing your symptoms. By integrating these approaches into your daily routine, you can experience considerable relief from joint pain. Your fear of movement will gradually diminish as you learn safe, effective ways to stay active. And you'll find your energy levels improving as you adopt the recommended techniques to combat fatigue.

Moreover, the book not only addresses physical symptoms but also provides guidance on managing the emotional and psychological aspects of EDS. Living with a chronic condition can be mentally draining, and this resource offers valuable strategies to help you maintain a positive outlook and manage stress. The combination of physical and emotional support can lead to a more balanced and fulfilling life.

I encourage you to give this book a try. It's a valuable resource that can empower you to take control of your symptoms and enhance your overall well-being. Remember, your journey to better health begins with informed and proactive steps. Let's work together towards your improved health and quality of life.