Guest guest Posted May 26, 2006 Report Share Posted May 26, 2006 Hi, I thought I would write a note about my problems with lyme and what I've been going through. Just a bunch of rambling I guess but here goes... I have had this disease for 20 years now. It has not only effected me buy also my family. I am very fortunate to have the greatest wife, son and parents that stand with me in my battle with this horrible illness. I am disabled and can no longer work. I have many symptoms and these are just a few. I have memory and comprehension deficits along with vision, speech, motor skills, tremors in my right hand, light sensitive, severe muscle and joint pain, weakness, have had several mini stroke type episodes, word finding skills, depression, having trouble walking due to severe pain and swelling in my hips and knees, using my hands, balance, bladder control and many more problems that I can go on and on about. This has made my life a living hell to put it mildly. I am on very heavy pain meds just to be able to move and they hardly even help at all. I can't go anywhere or do anything most of the time. The simple things that folks take for granted have become a major struggle for me. My wife is an angel who not only works, but she takes care of me and is my voice to the doctors and handles everything along with daily life with our 16 year old son, 2 dogs and a cat and balances this with work that has her busy 7 days a week. It has become a disease-by proxy for her and she suffers and I feel helpless to do anything. I am getting worse all of the time and have have IV antibiotics through a cathider that was in my chest. I have lost my career, hobbies, doing things with my family and am mostly usless. I am a prisoner inside my own body with my windows being my eyes. The doctors that I have now are doing the best they can but having been ill this long and with all of the damage done to my brain and body, they can only try to make me as comfortable as possible which really is not very good at all, but they are trying. It's been a very hard road but I am still here. Maybe reading this will help others see that they are not alone. Being a Lyme sufferer is like being a small fish in a tank of all sharks. There's not a lot of hope. But you can never lose hope. I tell myself this and I go day to day, love my wife and son, and keep going. It beats the alternative. Well that's it for now. Thanks, Rich Quote Link to comment Share on other sites More sharing options...
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