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I remember walking into the counseling center over three decades ago at the University Of Southern Ms. I told them I was feeling "down" a lot and was certain I had depression. So were they. Hence I did. After six sessions, I told the therapyist I was not feeling better. She assured me I would feel worse before I felt better. I told her my body didn't feel better. She said nothing. She was a counselor in training and had a new patient. She was happy. I was not. Then I decided that if I could land a decent job with a great salary, all my maladies would suddenly disappear I landed a job as chief writer and editor at a major network in Washington, D.C. At age thirty six. By age thirty seven, I had read enough about depression to know I had it. I immediately took action and visited a local psychologist who brought a psychiatrist aboard to try a combination of talk and medicine therapy. Year after year I religiously attended my therapy meeting and took my myriad of pills, combinations of pills, changing pills, increasing dosages of pills, etc. Nothing worked yet the medical community continued to applaud me for doing so much better. I begged to them that nothing had changed (I knew how I felt inside my body a lot more than they did), but they insisted the changes were so subtle, I would surely notice if I stopped taking my medicines and discontinued therapy. I did just that. No difference whatsoever. By then, I could barely work much less get out of bed. I made myself do it. I still don't know how, but felt I needed to. By 1994, I had moved to the west coast to pursue screen writing as I theorized that if I could just land one box office hit, happiness would land upon me and my (by then) severe depression and anxiety would be conquered. Anyone with any sense knows the outcome of that loser's game. And I lost. After taking a number of seminars and workshops on screen writing, and even writing several full- length motion pictures, I fell yet into a deeper depression. I went back into therapy and continued on the newer SSRI drugs, which the medical community told me were "nearly foolproof". I am glad they mentioned the keyword "nearly" as they were anything but. I remained a fool, thinking I would find an answer in a pill. It had not worked in the past, why would it now? But they assured me this new Prozac and family of similar meds worked when nothing else did. Then the Northridge Earthquake happened and ruined almost all my possessions. That same week, my mother called from Mississippi ill with cancer. I returned to care for her. Though I rarely had time to read magazines, one afternoon whil etaking mom to the doctor, I picked up a New Yorker in the waiting room. There was an article about a new experimental treatment called VNS (Vagus Nerve Stimulation) for something called TRD (treatment resistent depression). It was more common than once thought. The symptoms were explained and they were identical to mine. Though it had been available on the market for TRE (treatment resistent epilepsy) it was not yet available for TRD. But a small manufacturer, Cyberonics in Houston, the manufacturer of it, was in battle with the FDA and other powers that be. I started getting more and more curious and spent a great many hours on the Internet following the studies. It came close to FDA approval several times, but the powerful AMA and pharmaceutical lobbyists continued to "find fault" in the studies and kept it off. The battle raged on between Cyberonics and some very powerful medical and pharmaceutical lobbyists that kept finding fault in the studies. It would be delayed another several years. I simply had to wait and hang on by the skin of my teeth. Since I continued to "be punished" in my hometown (was very disenfranchised by then), I started to research. My search was focused on towns with low cost of living, high quality of life, and an advanced medical community. I was not finding any of that at home. Surprisingly Hot Springs, Ar became a top choice. The major medical community was in Little Rock, less than an hour away and UALR Medical Campus was considered one of the most advanced in the country (to my surprise). It's name was and is up there with many more familiar names like Sloan-Kettering, M.D. Anderson, and Johns Hopkins. In September of 2005, I finally heard that VNS therapy had been approved by the FDA for treatment of TRD. To my knowledge, it was the only medical modicum that had been approved for such. Now the problem was how to "get my name on the list". So I called Cyberonics and they turned me over to a nurse/caseworker, who got right on the case. She found the (very few) surgeons who performed this one hour procedure, and she had to talk my insurance into covering it based on my medical history of years of no results. On January 25, 2006, almost nine years after I first started following the news of the VNS implant, I received the procedure in Little Rock, Ar. at St. Vincent's Hospital. I remember waking up and feeling very light. Something had happened, but I was not sure what. I knew almost immediately that I'd gotten the procedure. I asked a nurse if "it was in" and she assured me it was. For the first time since I was about twelve years old, I felt no depression? I still had some anxiety but it was based on thinking "my mood is about to swing any minute and there is not a damned thing I can do about it". Minutes passed by and then hours. No mood swing. I felt like a child playing in the sandbox in kindergarten My worries and stresses were minimal. Every month, I continued to go to Little Rock for a computerized non-invasive "tune up"; the doctor merely turns up the frequency another notch. It is at a point now where it is every three months and by the end of the year, the depression will be in total remission. How is my progress? Amazing. I can remember like yesterday that I could not get out of bed, it was a huge chore to clean my home, studying was a brutal task as was work, and all that changed. I love what I do, I do it well, and do it joyfully. Today I am a cartoonist and etailer and full time student, have a wonderful girlfriend, and all kinds of doors opening that were closed, due to my having a undiagnosed disease, and at that, one that was not only socially-unnacceptable but one that a lot of people do not believe exists. My faith is back and if others have problems with my disease and recovery, I believe it reflects more on them than on me. VNS, for me, is the closest thing to a miracle I've ever experienced. It is not a cure-all, yes I still occasionally get the blues. I guess medicine offers no panaceas. But this is the closest thing to one I've ever experienced. Many friends and associates suggested I not reveal this story, that people might use it against me. My reply is "So what? Let them use it. If one person reads this with TRD and learns about it, and is fortunate enough to receive the implant, people can use it against me all they want. Doesn't matter in the least. Let one person get well from this most dreadful disease and it's all worth telling the story. Really. Well, back to work. If you really want to, you can enjoy the rest of your life. Please do so!
Article Source: http://www.search4allinfo.com
Rick London was told for 35 years he had garden-variety depression but the doctors were mistaken. Waiting for VNS to be approved London focused on his Londons Times Cartoons comic art gifts, and funny t-shirts
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