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I am pretty new to this Neuropathy thing, mine got really bad in July of last year and it took til October for them to diagnose and then another few months in pain management to get some relief to the point I wasn't in a ball in my bed sobbing to my husband.
From July 13-Mar 14 I was in so much pain I was like a crazy woman who begged every single doctor I saw to please help me. I never knew until then that your brain can be so consumed pain to the point it was all I thought about was begging for help.. If you knew me you would understand that that is waaay out of character for me. I am generally a very independant suck it up type of person and I was a mad woman. I soaked my feet in ice, plunged my feet in snow piles, kept buckets of ice next to my bed to soak my feet in when I woke up in the middle of the night (if I slept at all) I tried using sunburn gel with lidocaine in it to try and numb the pain. I was literally bathing in sunburn gel lol. During that time they had me on many different meds and kept raising the doses of my gabapentin to max dose of 3600mg. My pain doctor asked me to try Nucynta ER. After the first week on it I was still begging for help calling them telling them it wasn't working. They told me to wait it out and if it wasn't working by my appointment date we would try something else. Like I said before after about 3 weeks the pain relief was so much better than any of the other treatments I had tried so far. I have been on it since March along with now Lyrica and that combo seems to help enough I can actually function most days to the point I can even go grocery shopping and for small walks where I couldn't before. You have to understand that with any drug there is a chance of dependency. I know I have to be on these types of drugs for the rest of my life. I know that this neuropathy is never going to get better doctors told me that not long ago, so I needed to decide the risk of the med vs dependency and other side effects and I have chosen to give it a try for the relief it gives that allows me to function at least a little bit. |
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There are also a host of other ailments that we get as we get older and these to are masked by pain killing drugs so when we try to stop its hell. There is a also a psychological factor both with antidepressants and pain killers like tramadol that help us deal with the disease by numbing the senses and telling us sure we are sick but I don't care to much about it, now there is a big dependency right there. I cant see how anyone with serious pain issues can not become dependent. |
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I am at the beginning. I am thankful that between the two medicines I take I get marginal relief. Some days are good and they seem to allow me to make it through my work day with enough energy to get mobile quality family time in. Some days- stretches of days- I have to take more the secondary medication than I might want to.
I have made significant lifestyle changes that leave me at the odd life juncture of- best shape of your life since you were an athlete (20 years ago) while having a chronic condition that is often extremely dibilitating. These ebbs and flows left me reeling earlier this year. I thankfully had a secular Road to Damascus moment and decided that I had to keep positive. So I do my best to lead with that. Results, as always may, er do vary. I have lowered the intake of one medicine while increased the other. I no longer wait to see if I can withstand a bad day. I have been caught behind the curve of the pain that way. It takes five minutes of stretching to know which day it will be. I know it may come to a day where it takes five minutes of trying to get out of the bed to consider stretching. It is a tough decision on how to handle it. Such an individual one too. My wife is in on all of it. I have my kids to consider and they are both young. Thanks to many of the suggestions here- Salonpas - I have found some OTC stuff that at least helps take some edges off a tad. It is a matter of degrees at times. My best to all. Jon |
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Sorry for the rambling. |
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