History of MS: 19th century
19th century Until the early years of the 19th century, physicians relied on superstition, hearsay, and “the wisdom of the ancients” to care for the sick. Medical ideas were not scientifically tested. Even so, physicians were often good observers and we can look back today and identify people who undoubtedly had MS from descriptions written as long ago as the Middle Ages. Drawings from autopsies done as early as 1838 clearly show what we now recognize as MS. Then, in 1868, Jean-Martin Charcot, a professor at the University of Paris who has been called “the father of neurology,” carefully examined a young woman with a tremor of a sort he had never seen before. He noted her other neurological problems including slurred speech and abnormal eye movements, and compared them…
History of MS: 1900 – 1960
20th century In the 19th century, scientists first learned that bacteria cause many diseases. As the 20th century began, they discovered even smaller organisms, viruses, and developed techniques for growing and studying bacteria and viruses in the laboratory. This later led to research on viral causes of MS. In 1906, the Nobel Prize for Medicine was awarded to Dr. Camillo Golgi and Dr. Santiago Ramon y Cajal, who perfected new chemicals to enhance the visibility of nerve cells under the microscope. With this new technology now available, Dr. James Dawson at the University of Edinburgh in 1916 performed detailed microscopic examinations of the brains of patients who had died with MS.
MS News: August 2014
August 2014 has been a great month for people with neurological illnesses, as they finally saw their type of illness broadcast, and indeed, doused by ALS ice bucket challenges. To quickly place ALS amongst other neurological illnesses, perhaps the most famous person with ALS is Stephen Hawking, a personal hero of mine since my teenage years. ALS, also called MND (Motor Neurone Disease and Lou Gehrig’s Disease), is similar to multiple sclerosis and has several causes. A lot of money has gone to charitable organisations supporting ALS as well as other neurological illnesses.
A day in the life of fatigue
The Spoon Theory
Today I was reminded of a story I heard of a few years ago about a girl who lives with lupus and who tries to explain to a friend what life with a chronic illness, especially fatigue, is like. It is told in a very powerful and imaginative way that will hopefully shed a better light on how fatigue affects people living with MS, lupus and other illnesses that take a toll on daily life. In my view, it is the best piece of writing about fatigue I have ever read. As you know, one of my main disabilities is severe fatigue which is sometimes so energy-sapping that walking from my bed to the fridge asks for a rest in between. From the moment this level of tiredness became troublesome,…
World MS Day 2013: be informed
What is MS?
WMSD 2013: cure ignorance