DR. KEIRAN MURPHY IS NO LONGER ACCEPTING APPLICATIONS
FOR THIS RESEARCH PROJECT
FINAL RESULTS SHOULD BE AVAILABLE BY THE END OF FEBRUARY 2014
IF YOU ARE A PATIENT, WITH QUESTIONS PLEASE EMAIL;
s.jones@tarlovcystsociety.com
March of 2013 marked the three-year anniversary of my introduction to the world of Rare Disease.
It was March of 2010, three months after a Motor Vehicle Accident triggered excruciating pain when my first MRI’s were ordered. Within days I was introduced to the rare disease known as Tarlov Cyst Disease.
Before the accident I’d been living with some occasional, and other longstanding symptoms explained only by the unique set of symptoms that appeared at any given time. When the diagnosis of Fibromyalgia was added to the list in 2005 it became the catchall for every old or new, pain and symptom.
I’d grown accustomed to some of my health issues and accepted them as a normal part of life, but thanks to two MRI’s and several informed and experienced specialists I finally discovered that what I suffered from was far from normal.
The symptoms and insurmountable pain that accompanied my post-accident problems could only be described as living through a nightmare full of pain, fear, anger and confusion. I watched the life I knew quickly slip away while a new pain filled, devastating, but determined and inquisitive life began.
I will always consider myself to be blessed. Not because I’m ill, or because I can research or write, but because everything I’ve needed, short of an all encompassing solution, has found its way into my life, providing the things I needed at the appropriate stage or time.
I started writing my blog shortly after diagnosis while searching for answers and others like myself. Since the beginning of the blog I’ve met hundreds, or perhaps even thousands of people living with many of the same symptoms and fears I know only too well. My blog allowed many newly diagnosed patients to find out more about their diagnosis and its helped guide patients to other patients and to some of the few specialists who offered care. Some assistance was minimally invasive, while others were informative, but the blog began to show the world how large our little Tarlov World had become.
Unfortunately the number of Canadians diagnosed with this disease has grown in numbers, and our little Tarlov Cyst Society continues to grow with it. Our society has grown from none in the beginning, to at least one Tarlov Cyst patient in every Province across the Country. Some Canadians found connection through this blog, others through some of the many support groups formed by patient advocates around the world.
For some reason the highest population of Tarlov Cyst patients in Canada live within the Province of Ontario, which for the following announcement is certainly a benefit to Canadians and all Tarlov Cyst Disease Patients around the world.
That information has buzzed on the support groups, been wondered about by patients, and prayed for by all. It announcement informed us of a one-year Tarlov Cyst research grant had been funded by the Tarlov Cyst Disease Foundation. The one year grant has been implemented for the Foundation by NORD (National Organization for Rare Disorders).
The grant recipients were:
Principal Investigator: Kieran Murphy, MB, BCh, FRCPC, FSIR
Professor & Vice Chair, Medical Imaging
Deputy Chief, Medical Imaging, University Health Network,Mt Sinai Womens' Hospital
Director, International Medical affairs, University Health Network, Toronto Western Hospital
University of Toronto, Ontario, Canada
In addition to this announcement I’ve been authorized to inform Tarlov Cyst Disease patients within, Ontario, Canada, that they are invited to take part in the following study;
“A genetic analysis of patients with Tarlov cysts”
The study is led by Dr. Kieran Murphy at Toronto Western Hospital.
The purpose of the study is to determine whether or not there is a relationship between Tarlov cysts and three connective tissue syndromes, (Marfan, Loeys-Dietz and Ehlers-Danlos syndromes).
Participants will be assessed by a clinical geneticist who will determine any features associated with these syndromes. Those participants who show one or more features will go on to have genetic testing of those genes associated with the three connective tissue syndromes (a blood sample will be taken). The appointment will take approximately 2 hours.
If you, or anyone you know are interested in taking part in this study please contact
Abby Skanda - askanda@uhnresearch.ca
the study coordinator who will contact you directly.
This is an exciting time for Tarlov Cyst Disease Patients within Ontario, Canada and around the world. For the first time in Canada researchers will be searching for answers to some of the many questions on the minds of every patient, family member or friend of a person diagnosed with this dreadful disease.
Please come forward, let your pain and suffering help Dr. Murphy and his staff find the answers we all need.
This is for me, my TC Cysters, our families and for the many generations to come.
With love to all!
Sherri Jones
Please forward all information and inquiries to;
Abby Skanda - askanda@uhnresearch.ca
