Guest guest Posted October 25, 2008 Report Share Posted October 25, 2008 I have been a member of this group for months but was too ashamed to post. I kept listening to others and telling myself to " be strong " . I really need to get this out, please be patient with me. I am a MS patient and I was diagnosed 2 years ago. I had to retire and since then I spend most of my days home alone and in pain. I stopped telling my long lost friends and family (they don't really care when they say - how are you?). I have horrible spasticity and the spasms wake me screaming at night. I have a reginimen of about 5-6 meds a day and now I supplement that with a glass of wine, and I still can't get through the night. The spasms are in cycles and they involuntary shaking is so bad and so painful that I look like I might be having seizures. My body has to go through a 10-15 minute cycle of spasms and then it usually subsides and I am so exhausted from trying not to scream at the top of my lungs. Pain sends you to such a deep level of despair that only someone that has walked the walk can understand. My pain comes through tranquilizers and yes I do see a MS specialist, a Neuro, a PM specialist and my Primary on a regular basis. Thanks. Any ideas for coping will greately apreciated. Thanks for listening, I am running out of courage. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2008 Report Share Posted October 26, 2008 voogee wrote: > I have a reginimen of about 5-6 meds a day and now I supplement that with a glass of wine, and I still can't get through the night. The spasms are in cycles and they involuntary shaking is so bad and so painful that I look like I might be having seizures. > My body has to go through a 10-15 minute cycle of spasms and then it usually subsides and I am so exhausted from trying not to scream at the top of my lungs. You really have your plate full. I trust that the doctors are giving you something like a strong dose of Baclofen or another anti spasmodic to help with the spasms? If they are and it's not working, they need to address that issue immediately. Please don't supplement your medications with alcohol. That can easily lead to even more problems than you have already. -- Lyndi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2008 Report Share Posted October 26, 2008 Rich, I cannot begin to tell you the hell I have been through because I did not have the support you seem to have had. The pain alone was bad enough but I was determined not to let it beat me. But because of the lack of support one needs, my life has turned from a 28 year sucessful career, a 15 year marriage, a beautiful home, lots of friends and a big family to losing them all because my life of friends and family were so intertwined. A sequence of events so absurd unfolded on me I would not know how to begin to tell my story or if it would do me any good. All I can say is it has made me a very sick man inside on top of my chronic back pain. I am on the edge of losing this battle because I am now alone in this world and feeling terribly beaten and it all started with my back problems after surgery. >Rich S. wrote: > I was forunate to become a member of a local pain clinic. Besides > treating my extreme low back pain, they also had a psychologist on > staff that I met with several times. Although I still feel the loss > of my career on some levels, the counseling really helped me. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2008 Report Share Posted October 26, 2008 Hi vboogee I also have MS and suffer horrible spasms and pain. I know exactly what you are talking about. It's a pain that is hard to describe to someone who doesn't have it. You are definetely at the right place. Even though a lot of us suffer different types of pain one thing is for sure and that's that we all know what pain is. We all understand the words in your post. Never be ashamed to post here. No one will ever judge you or think you are over exaggerating your pain. We all know and we all care what you are going through. What medications are you currently taking? Are you currently taking anything specifically for MS? What type of MS do you have? It's okay if you don't feel like answering these questions. As long as you know that no one will ever judge you here. If you would like to e-mail me privately we could talk a little more in depth about our MS and I could give you some good sites to check out. Your in my thoughts and Prayers, Carol (OK) > vboogee wrote: > Pain sends you to such a deep level of despair that only someone that has walked the walk can understand. My pain comes through tranquilizers and yes I do see a MS specialist, a Neuro, a PM specialist and my Primary on a regular basis. Thanks. >Any ideas for coping will greately apreciated. Thanks for listening, I am running out of courage. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2008 Report Share Posted October 26, 2008 Hi Lyndi, Don't know if this is the first time I've posted here. I've been a quiet back seat driver for a long time, and have got a lot out of just reading. I can't keep up with being an active member of everything. I Just saw your post, and something a doc said to me a long time ago when I was about 23yrs old (I'm 42 now) when I was having trouble sleeping, because of pain from two work accidents and to car accidents in a 2 year space of time. The doc recommended having a " glass of port " each evening. Didn't take up his idea because I've never drunk anything alcoholic in my life when it comes down to it. The only alcoholic stuff I've drunk is what's in cough syrup. And I wasn't going to start back then. I know a lot more now than I knew then and know enough about not mixing most meds with alcohol. Especially pain meds, and antidepressants and epileptic meds, not good combing them with alcohol. Thankfully medical advice has changed over the years. Pam Vic Oz Cats aren't clean ... they're just covered in cat spit! Quote Link to comment Share on other sites More sharing options...
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