The Pituitary Patient Bill of Rights
|As a patient afflicted with a chronic, often lifelong disease, I wish to affirm the following:
I did not bring this disease upon myself through any form of omission or commission.
I know, however, that my illness and its many symptoms and manifestations are poorly understood, and often imperfectly treated, with results that are unacceptable in any medically civilized society.
I affirm that I am a valuable human being: to myself, my family and the society in which I live and work. My right to proper diagnosis, care and management shall be second to none.
Either I or my fellow patients may have our lives and the length and quality of life at constant risk.
I cannot allow my rights as a member of society to be trampled on. I realize that it is not currently politically popular to give me my fair share of quality medical care, research, education, and mental, moral, psychological or societal care.
For these and other reasons and on behalf of myself, my loved ones, my family, and my fellow patients, I claim the following:
Pituitary diseases, tumors and the resultant hormonal imbalances shall be recognized as a serious, major public health problem afflicting a large segment of the world’s population.
The financial and intellectual resources of my government and our public and private health services shall be as fairly allocated to me and my disorder as they are to any other life-threatening and life-altering disease.
I have a right to an early and appropriate diagnosis, treatment, care and medical intervention by the experts in these fields of medicine.
I have an inalienable right to be told of – and allowed to use, whenever possible, any and all medications and treatment methods past, present or future – which will complete or assist in my healing.
Upon completion of any medical evaluation, treatment and care, I am entitled to the emotional and psychological care afforded anyone else with psycho-socially affective disorders.
I reaffirm my right to be treated completely so I may reclaim my place in society and my family as a fully functioning and contributing member.
I shall not be discriminated against in my workplace or any other part of society because of my physical, mental or emotional state.
There shall not be any financial, insurance, job, or promotional stigma attached to my disease’s discovery, medical care or emotional recovery. My future life shall only be limited by conditions not under man’s ability to rectify.
My family and coworkers have a right to be informed and counseled about my illness and Its many manifestations. In order for them to understand and accept the temporary limitation to my job performance and my family obligations, they must if possible, become part of my healing environment.
I reaffirm to the world: I am a valuable member of the society and family of man. My life is too valuable to waste. It is too costly to society and too detrimental to my family to allow me to merely exist at their sufferance and largesse.
I have the right to be believed! Just because a physician has not yet heard of, or seen, my symptoms before, does not mean they are not real and deserving of medical care and further investigation.
With permission from:
Recent Posts: Not Over Till The Fat Lady Sings
- January 2019
- December 2018
- November 2018
- October 2018
- September 2018
- July 2018
- June 2018
- May 2018
- April 2018
- March 2018
- February 2018
- December 2017
- November 2017
- October 2017
- September 2017
- August 2017
- July 2017
- March 2017
- June 2014
- November 2013
- September 2013
- August 2013
- July 2013
- May 2013
- March 2013
- February 2013
- December 2012
- November 2012
- October 2012
- A Bit About Me – Introduction
- Guest Stories
- Cynthia’s Story
- Arlene’s Story
- Barbara’s Story
- Dean Kramer Story – Out of My Mind
- Denyse’s Story
- Donna’s Story
- Helen’s Story
- Jan’s Story
- Jan’s Story – A View From the Other Side
- Jan’s Story – Hip Replacement Surgery With Addison’s Disease
- Jan’s Story – I’m Not Fat, I’m On Steroids
- Jan’s Story – Looking Out for Yourself
- Jan’s Story – St. Katharine Drexel Sent Me An Angel
- Jan’s Story – The Second Time Around
- Jan’s Story – This Is What It Feels Like To Wean
- Jody’s Story
- John Moody’s Story
- Kathleen Houghton’s Story – The Thief of Many Lives
- Kay’s Story – Graves’ Disease, Fibromyalgia & PCOS
- Kaybee’s Story – My First Root Canal
- Lisa’s Story
- Patricia’s Story
- Sara W’s Story
- Sherrie’s Story
- Steve’s Story
- The Thief of Many Lives
- Tired of Being Me
- Trish’s Story
- Victoria’s Story – What is IT?
- Information and Symptoms
- Contract For An RAI Pushy Doctor
- Deciphering Commonly Used Acronyms/In Reference to Thyroid Issues
- Finding Elusive Pheochromocytomas
- Hypothyroidism and Breast Cancer – Modern Day Epidemic
- Patient Self Assessment Form/Quality of Life Assessment
- Symptoms of HyperactiveThyroid
- Symptoms of Hypothyroid
- Top 22 Reasons Not to Have RAI (Radio Active Iodine)
- When And How To Treat The Not So Typical Patient
- LOL – Laughing Out Loud