<?xml version='1.0' encoding='UTF-8'?><?xml-stylesheet href="http://www.blogger.com/styles/atom.css" type="text/css"?><feed xmlns='http://www.w3.org/2005/Atom' xmlns:openSearch='http://a9.com/-/spec/opensearchrss/1.0/' xmlns:georss='http://www.georss.org/georss' xmlns:gd='http://schemas.google.com/g/2005' xmlns:thr='http://purl.org/syndication/thread/1.0'><id>tag:blogger.com,1999:blog-1069975608476122322</id><updated>2011-11-27T17:24:11.465-08:00</updated><title type='text'>Living With Multiple Sclerosis</title><subtitle type='html'></subtitle><link rel='http://schemas.google.com/g/2005#feed' type='application/atom+xml' href='http://mswithnofear.blogspot.com/feeds/posts/default'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/1069975608476122322/posts/default?max-results=100'/><link rel='alternate' type='text/html' href='http://mswithnofear.blogspot.com/'/><link rel='hub' href='http://pubsubhubbub.appspot.com/'/><author><name>Enda Sheridan</name><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><generator version='7.00' uri='http://www.blogger.com'>Blogger</generator><openSearch:totalResults>3</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>100</openSearch:itemsPerPage><entry><id>tag:blogger.com,1999:blog-1069975608476122322.post-1787035626260387542</id><published>2009-11-17T07:50:00.000-08:00</published><updated>2009-11-17T07:51:25.522-08:00</updated><title type='text'>fatal flaw in Tysabri</title><content type='html'>When Anita Louise Smith enrolled in an experimental drug trial in 2002 in Colorado, she had a diagnosis of multiple &lt;br /&gt;&lt;br /&gt;sclerosis but, no symptoms and was looking to reduce the chances of being ravaged by the disease. Last year, she &lt;br /&gt;&lt;br /&gt;died at the age of 46 from an infection linked to the drug.&lt;br /&gt;&lt;br /&gt;This tragedy - recounted in an article in the March 4 issue of The Lancet by two Stanford University School of &lt;br /&gt;&lt;br /&gt;Medicine neurologists - serves as a telling case study of what can go wrong in clinical trials. In their article, &lt;br /&gt;&lt;br /&gt;Annette Langer-Gould, MD, and Lawrence Steinman, MD, warn of the pitfalls of testing a drug with unknown side &lt;br /&gt;&lt;br /&gt;effects in patients who would do fine without the drug.&lt;br /&gt;&lt;br /&gt;The drug in question is natalizumab, which has the brand name of Tysabri. In November 2004, the U.S. Food and Drug &lt;br /&gt;&lt;br /&gt;Administration fast-tracked its approval for use in multiple sclerosis patients following promising results seen &lt;br /&gt;&lt;br /&gt;early in two clinical trials. But within months of the approval, some patients taking the drug had developed a rare &lt;br /&gt;&lt;br /&gt;infection - progressive multifocal leukoencephalopathy, or PML - and Smith and one other patient had died.&lt;br /&gt;&lt;br /&gt;Langer-Gould, a clinical instructor in neurology, treated a patient who was part of the clinical trial and developed &lt;br /&gt;&lt;br /&gt;PML after taking Tysabri; the patient survived. But that experience, coupled with an examination of Smith’s case, &lt;br /&gt;&lt;br /&gt;prompted Langer-Gould to approach Steinman about writing an article that would examine the appropriateness of &lt;br /&gt;&lt;br /&gt;testing a drug on people with no evidence of the disease and who are not disabled at the time of the trial.&lt;br /&gt;&lt;br /&gt;We are arguing that people with no disability should probably not enter into a clinical trial or be &lt;br /&gt;&lt;br /&gt;recruited into clinical trials, because where is the potential benefit to them if nothing is wrong?"; said &lt;br /&gt;&lt;br /&gt;Steinman, professor of neurology and neurological sciences and of pediatrics.&lt;br /&gt;&lt;br /&gt;This situation represents a systemic problem, said Langer-Gould. It is not just one company &lt;br /&gt;&lt;br /&gt;being a rogue, doing something out in left field.";&lt;br /&gt;&lt;br /&gt;Langer-Gould and Steinman argue that if a drug has a known risk of death, it should only be used on patients who are &lt;br /&gt;&lt;br /&gt;likely to suffer severe disability from the targeted disease - and for whom there are no other options. In other &lt;br /&gt;&lt;br /&gt;words, those who have tried all the other available therapies. That is almost the reverse of what happened in the &lt;br /&gt;&lt;br /&gt;Tysabri trial, which excluded the most severely affected patients.&lt;br /&gt;&lt;br /&gt;";A big mistake was made in these trials that, in my opinion, is easily preventable,"; said &lt;br /&gt;&lt;br /&gt;Langer-Gould. ";All they need to do is tighten up entry criteria into multiple sclerosis clinical trials and &lt;br /&gt;&lt;br /&gt;we could avoid similar types of problems in other trials.";&lt;br /&gt;&lt;br /&gt;Multiple sclerosis results when the immune system attacks the protective myelin sheath surrounding nerve cells, &lt;br /&gt;&lt;br /&gt;causing them to misfire and leading to loss of motor control and possibly paralysis. Tysabri appeared to block this &lt;br /&gt;&lt;br /&gt;effect and, after the first year of the two-year clinical trials, did not appear to cause more infections.&lt;br /&gt;&lt;br /&gt;Steinman was involved early on in the development of the drug, publishing on its effects in 1992. Even then, he had &lt;br /&gt;&lt;br /&gt;suspicions that the drug’s mechanism of action - blocking the entry of immune cells into the nervous system - might &lt;br /&gt;&lt;br /&gt;also make patients more vulnerable to infections. Indeed, PML is an infection that usually affects people whose &lt;br /&gt;&lt;br /&gt;immune systems are compromised.&lt;br /&gt;&lt;br /&gt;";It was a shocking development that a drug that had so much promise and so many potential benefits ended up &lt;br /&gt;&lt;br /&gt;causing two deaths and one very serious injury,"; said Steinman. ";It is kind of a cruel Greek drama, &lt;br /&gt;&lt;br /&gt;something that may be more beneficial than anything yet developed for multiple sclerosis, but yet may be far more &lt;br /&gt;&lt;br /&gt;dangerous than those other approved drugs.";&lt;br /&gt;&lt;br /&gt;The FDA withdrew Tysabri only three months after its approval. The FDA is now considering re-approving the drug. On &lt;br /&gt;&lt;br /&gt;March 7 and 8, an FDA advisory panel is meeting about the possibility of bringing back Tysabri as a single therapy &lt;br /&gt;&lt;br /&gt;(in the trials, it was combined with another drug).&lt;br /&gt;&lt;br /&gt;";I predict it will come back with really hellacious warnings,"; said Steinman. ";I think the &lt;br /&gt;&lt;br /&gt;right course would be to have it undergo more testing, but I don’t think that is practical or fair to patients; they &lt;br /&gt;&lt;br /&gt;ought to have the opportunity to decide with their physicians if they are willing to take the one in a thousand risk &lt;br /&gt;&lt;br /&gt;of dying.";&lt;br /&gt;&lt;br /&gt;But Steinman and Langer-Gould expressed reservations about the drug returning to the market. They noted that its &lt;br /&gt;&lt;br /&gt;effects, while impressive, are in general not much better than what is seen with other available drugs: The risk of &lt;br /&gt;&lt;br /&gt;relapse dropped from an average of two relapses every three years using other approved multiple sclerosis drugs to &lt;br /&gt;&lt;br /&gt;one every three years with Tysabri.&lt;br /&gt;&lt;br /&gt;";Do you want to expose someone to the risk of death for eliminating one relapse every three years?"; &lt;br /&gt;&lt;br /&gt;said Steinman. ";I say no.";&lt;br /&gt;&lt;br /&gt;";I’m not sure if it is wise to re-approve it,"; added Langer-Gould. ";The question is, will the &lt;br /&gt;&lt;br /&gt;FDA rise to the occasion and admit their mistake and try to prevent future mistakes or are they going to ignore &lt;br /&gt;&lt;br /&gt;it?";&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/1069975608476122322-1787035626260387542?l=mswithnofear.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/1069975608476122322/posts/default/1787035626260387542'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/1069975608476122322/posts/default/1787035626260387542'/><link rel='alternate' type='text/html' href='http://mswithnofear.blogspot.com/2009/11/fatal-flaw-in-tysabri.html' title='fatal flaw in Tysabri'/><author><name>Enda Sheridan</name><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author></entry><entry><id>tag:blogger.com,1999:blog-1069975608476122322.post-2071781155751460301</id><published>2008-12-13T06:36:00.000-08:00</published><updated>2009-02-10T12:43:18.974-08:00</updated><title type='text'>....</title><content type='html'>&lt;span style="font-size:130%;"&gt;&lt;span style="font-weight: bold;"&gt;&lt;br /&gt;&lt;/span&gt;&lt;span style="font-weight: bold;"&gt;&lt;span style="color: rgb(51, 51, 51);"&gt;In 1988, Chris Sheridan was diagnosed with Multiple Sclerosis.&lt;/span&gt;&lt;/span&gt;&lt;span style="font-weight: bold;"&gt;&lt;br /&gt;&lt;br /&gt;&lt;/span&gt;&lt;/span&gt;&lt;span style="font-size:130%;"&gt;&lt;span style="font-weight: bold; color: rgb(255, 0, 0);"&gt;By 2005 he was completely housebound.&lt;/span&gt;&lt;br /&gt;&lt;span style="color: rgb(204, 0, 0); font-weight: bold;"&gt;&lt;span style="color: rgb(0, 0, 0);"&gt;Today &lt;/span&gt;&lt;span style="color: rgb(255, 0, 0);"&gt;Chris walks, drives, showers and cooks for himself and no longer suffers constant shaking, trembling, chronic fatigue, double vision or slurred speech...&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;br /&gt;&lt;span style="color: rgb(255, 0, 0); font-weight: bold;font-size:130%;" &gt;He now works a normal eight hour day and lives with his wife Yvonne and their two kids Jack and &lt;span class="blsp-spelling-error" id="SPELLING_ERROR_0"&gt;Saoirse&lt;/span&gt;.&lt;/span&gt;&lt;span style="font-size:130%;"&gt;&lt;br /&gt;&lt;/span&gt;&lt;br /&gt;&lt;span style="font-size:130%;"&gt;&lt;span style="font-weight: bold;"&gt;"MS With No Fear, 20 years living With MS" is the story of Chris Sheridan and how he has learnt to control and overcome all the symptoms of MS...&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;br /&gt;&lt;ul&gt;&lt;li style="color: rgb(255, 0, 0); font-weight: bold;"&gt;&lt;span style="font-size:130%;"&gt;He was diagnosed with Multiple Sclerosis in 1988.&lt;/span&gt;&lt;/li&gt;&lt;li style="color: rgb(0, 0, 0); font-weight: bold;"&gt;&lt;span style="font-size:130%;"&gt;Partially blinded in 1993.&lt;/span&gt;&lt;/li&gt;&lt;li style="color: rgb(0, 0, 0); font-weight: bold;"&gt;&lt;span style="font-size:130%;"&gt;Slurred speech in 1998.&lt;/span&gt;&lt;/li&gt;&lt;li style="color: rgb(0, 0, 0); font-weight: bold;"&gt;&lt;span style="font-size:130%;"&gt;Wheelchair bound in 2005.&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span style="color: rgb(255, 0, 0); font-weight: bold;font-size:130%;" &gt;He made a Full amazing recovery in 2006&lt;/span&gt;&lt;span style="font-size:130%;"&gt;&lt;span style="font-weight: bold;"&gt;.&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/li&gt;&lt;/ul&gt;&lt;span style="font-weight: bold;font-size:130%;" &gt;&lt;br /&gt;He has learnt to counteract all the negative feelings that go with this diagnosis.&lt;br /&gt;&lt;br /&gt;Through &lt;/span&gt;&lt;span style="font-weight: bold;font-size:130%;" &gt;&lt;span style="color: rgb(255, 0, 0);"&gt;his own unique ability and a very special process&lt;/span&gt;&lt;/span&gt;&lt;span style="font-weight: bold;font-size:130%;" &gt; he regained full strength in his legs and learnt to walk again.&lt;br /&gt;&lt;br /&gt;In his book "MS With No Fear",Chris details his full story and &lt;/span&gt;&lt;span style="font-weight: bold;font-size:130%;" &gt;&lt;span style="color: rgb(255, 0, 0);"&gt;explains just what he had to do to aid&lt;/span&gt;&lt;/span&gt;&lt;span style="font-weight: bold;font-size:130%;" &gt;&lt;span style="color: rgb(255, 0, 0);"&gt; his &lt;/span&gt;&lt;/span&gt;&lt;span style="color: rgb(255, 0, 0); font-weight: bold;font-size:130%;" &gt;FULL Recovery&lt;/span&gt;&lt;span style="font-size:130%;"&gt;&lt;span style="font-weight: bold;"&gt;.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span style="font-weight: bold;"&gt;He hopes  to help newly diagnosed people and their loved ones to come to terms with their diagnoses.&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;br /&gt;&lt;a href="http://stores.lulu.com/store.php?fAcctID=3360701"&gt;&lt;br /&gt;&lt;img src="http://www.lulu.com/services/buy_now_buttons/images/book_blue.gif" alt="Support independent publishing: buy this book on Lulu." border="0" /&gt;&lt;br /&gt;&lt;/a&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/1069975608476122322-2071781155751460301?l=mswithnofear.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/1069975608476122322/posts/default/2071781155751460301'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/1069975608476122322/posts/default/2071781155751460301'/><link rel='alternate' type='text/html' href='http://mswithnofear.blogspot.com/2008/12/hello-my-book-is-now-available-here_13.html' title='....'/><author><name>Christopher Sheridan</name><uri>http://www.blogger.com/profile/03861352208523590259</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author></entry><entry><id>tag:blogger.com,1999:blog-1069975608476122322.post-1946512558969158482</id><published>2008-12-13T03:43:00.000-08:00</published><updated>2009-11-11T00:39:54.503-08:00</updated><title type='text'>Hello My book is now available here.</title><content type='html'>My name is Chris Sheridan and i have been diagnosed with Multiple Sclerosis now for over twenty years. In this time i have gone through the pain of not knowing what this condition is about and what it may entail in the long run for myself and loved ones. I have educated myself about this condition and regularly meet with other Ms people. I was hospitalised in 2005 and wheelchair bound for over six months, i recovered by using a simple process which i am now willing to tell the world about in my book "MS With No Fear". Please feel free to purchase this book at the link below . &lt;br /&gt;Thank you, your friend forever Chris.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/1069975608476122322-1946512558969158482?l=mswithnofear.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='related' href='http://www.lulu.com/content/5310882' title='Hello My book is now available here.'/><link rel='enclosure' type='' href='http://www.lulu.com/content/5310882' length='0'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/1069975608476122322/posts/default/1946512558969158482'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/1069975608476122322/posts/default/1946512558969158482'/><link rel='alternate' type='text/html' href='http://mswithnofear.blogspot.com/2008/12/hello-what-is-this-blog-about.html' title='Hello My book is now available here.'/><author><name>Enda Sheridan</name><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author></entry></feed>
