{"id":169,"date":"2004-06-30T17:46:16","date_gmt":"2004-06-30T15:46:16","guid":{"rendered":"http:\/\/home.tjerngren.net\/wp\/?p=169"},"modified":"2004-06-30T17:46:16","modified_gmt":"2004-06-30T15:46:16","slug":"striking-a-balance","status":"publish","type":"post","link":"https:\/\/www.beverlyrevelry.com\/?p=169","title":{"rendered":"Striking a balance"},"content":{"rendered":"<p>Three days before my twenty-fifth birthday, on April 16, 1998, I was diagnosed with multiple sclerosis.  By that time I&#8217;d been having a number of worrisome neurological symptoms for about three years, and it came as a relief to have a diagnosis.  First, because it was good just to be able to put a name to what was wrong with me, and second, because it lifted an enormous weight to know that I wasn&#8217;t facing something life-threatening (when the neurologist said it was MS, I asked, &#8220;I&#8217;m not going to die, am I?&#8221; and he replied, &#8220;Well, you&#8217;re going to die, but not from <i>this<\/i>,&#8221; which was the perfect mood-lightening response).<\/p>\n<p>Since I was diagnosed six years ago, I&#8217;ve had a fair amount of ups and downs.  For the first 2\u00bd years after diagnosis, I gave myself a weekly interferon shot but since moving to Sweden I haven&#8217;t been taking anything at all.  My condition was about the same both on interferon therapy and off, and I averaged three to five significant flare-ups per year.  Most of my flare-ups have been centered on my left leg, which just stops working for a couple of weeks now and again, and I do have some residual weakness there that seems to be permanent disability.  Overall, though, I consider myself very lucky in that I have what appears to be a mild case of MS, with no visible disability after almost ten years of symptoms.  The bulk of my symptoms are sensory, which is a blessing in that they don&#8217;t impair function and a curse in that they are at times excruciatingly painful.<\/p>\n<p>A little over a year ago I started reading up on managing MS through diet, and while I was somewhat skeptical, I started taking a vitamin-B supplement and 2000mg of Omega-3 oil every day.  The difference they&#8217;ve made has been truly astounding.  Since mid-April 2003, I have not had even one flare-up.  There were a couple of days last fall when I had some noticeable weakness in my arms, and I still have some sensory symptoms and the aforementioned weakness in my left leg, but I haven&#8217;t experienced any loss of function in over fourteen months.  For me, Omega-3 has been like a miracle cure.<\/p>\n<p>Last night, though, and this morning, I felt some of the sensations that have often signaled an oncoming flare-up.  It&#8217;s difficult to explain just what those sensations are, but after almost ten years I&#8217;ve learned to recognize the feelings.  It&#8217;s too early yet for me to tell whether or not those feelings will turn into a flare-up, but I&#8217;ve gotten so used to living without them that this has thrown me a bit for a loop.  Even though I know it&#8217;s not true, there&#8217;s a little part of me that&#8217;s been thinking maybe I really have beaten this, and the thought of even one more flare-up is discouraging as hell.  It&#8217;s really hard sometimes to find a balance between the optimistic and the realistic.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Three days before my twenty-fifth birthday, on April 16, 1998, I was diagnosed with multiple sclerosis. By that time I&#8217;d been having a number of worrisome neurological symptoms for about three years, and it came as a relief to have a diagnosis. First, because it was good just to be able to put a name&hellip; <a class=\"more-link\" href=\"https:\/\/www.beverlyrevelry.com\/?p=169\">Read More <span class=\"screen-reader-text\">Striking a balance<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-169","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=\/wp\/v2\/posts\/169","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=169"}],"version-history":[{"count":0,"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=\/wp\/v2\/posts\/169\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=169"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=169"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.beverlyrevelry.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=169"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}