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Electron |
No criticism intended....I too, use hydrocodone, which I don't see being able to give up....unless there is some magic pill or miraculous recovery.
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One more thing I want to make crystal clear....physical dependence on a medication is not addiction.
One can be physically dependent on many meds....even allergy pills....your body gets used to them and has a fit when it doesn't get them...even if you have no emotional attachment. That fit the body has, is, very much like the feelings of neuropathy....burning, restless legs, etc.... The only caution I have is to be more skeptical of those benzodiazepines.....they may seem to fix a problem, such as anxiety, only to produce a physical withdrawal between doses....it's a grind....I know....but if you need it, you need it and everything in life, basically boils down to risk versus benefit. You are not being judged. It is just prudent to look at medications first when analyzing any symptoms. |
Topaz? I hope that I've not said anything critical?
I understand that the docs can often be 'critical' enough for all of us! And docs can take the brunt of prescribing meds. My own docs are pure cheapskates in doling out the 'painkillers' [not that they do really much good? just salve my conscience] But, sometimes? Getting additional concrete valid opinions by super-or above-average specialists CAN help you on to a diagnosis and then treatment!
IF I ever found something that really worked for me? I'd be chomping the pills down faster then M's! To get a GOOD and whole night's peaceful sleep? Is something I sure would like to get! Hopes and prayers that you do too! Don't forget tho, that each of us comes here from a wide variety of diagnostics and experiences and doctors....good and bad. Only YOU good person can find your way thru the testing and meds morass to get the help you need! Don't ever let them tell you you are wrong. YOU KNOW WHAT, at least, isn't RIGHT! Keep at it, it's a hard road, but it can prevent 'things' from getting worse. I've a friend who's been wrestling the bi-polar and anxiety bear? I do believe that PN pain on top and all that goes with both...sure doesn't help things overall. It is NOT FUN! Hugs to you, and stop beating your head against an ungiving wall! My heart is with you and FOR you! Bravery is the only way I can think of you! :hug::hug::hug:'s - j |
thanks
i'm sorry if i seem defensive but you get so many people who want to tell you not to take anything. when i first came down with this disease i really thought i was dying. the medications have been a lifesaver. i too have some concerns about being on a lot of medication. it does hamper ones life to a certain degree. i just feel that my pn is getting worse again and i wanted a few opinions from those who have been were i am. sorry if i jumped to the wrong conclusion. thank you all for taking the time to chime in.
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PN makes me think I am dying sometimes.....I have autonomic issues as well and frankly, NUTHIN works right any more....add in the pain. I too, don't like being told I can't take a pain medication.
For me, it seems the pain always up the ante....up the dose....pain ups the ante. I found the way I have to do it is, lower the dose....feel the pain, then resume taking meds....or take a med holiday or some garbage. With dysautonomia, meds complicate things and make for even more problems....however, at times I can't stand it anymore and I MUST use meds, especially if my work load here at home increases. I don't have the option of 'reducing' my work load. It does feel at times, like you have been robbed of your life, but, this is the card we drew.....and it IS hard to find people who understand the relentless pain and disability, especially when PN is described as affecting only the feet, with numbness and tingling. |
Don't forget? We come here from soo many different ...
perspectives!
I worry about taking 'some pills w/other pills' because I've learned later that it wasn't good to just swallow 'em all at once in the morning! It can take me all day to take ALL my meds and supplements-some hours apart and others just to be safe each other hour! Can become an all day thing? But you do what you gotta do and only YOU know what that can be. But, being INFORMED [and often confused...know I've been that] comes with the territory. Just keep asking questions and you'll get a room full of answers? But maybe one room will feel just what you need. As for some ?'s on meds? This is our forum for that: http://neurotalk.psychcentral.com/forum72.html As for supplements?: http://neurotalk.psychcentral.com/forum49.html Peppermint Patty? THIS last one is the one you need to cruise thru! Mrs D [who is on vacation now, and a well deserved one?] Has been a rock of sanity and info about calciums, and other supplements. Don't try to read it all at once tho? Your brain can turn to mush if you 'overdose' on all this info! Hugs to all! :hug::hug::hug:'s!!!!!!!!!!! - j |
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I am on vacation and only have a short time on this wifi...
But I'd like to welcome you here to our forum. I see two glaring things... Prilosec will deplete several nutrients over time: B12, folate calcium magnesium zinc iron I think you should get a B12 test done ASAP and also have Vit D done. People who use alot of medications often get depleted in nutrients and it can be different for different drugs. I don't have my references with me but I do have that Prilosec memorized...it is very common and I post it often. Muscles require many things, including B6 for proper functioning. High doses of Prozac can also cause movement disorders but it is unclear if you have that exactly. This site gives a summary of some depletions so you can look at that until I get back. Some drugs are too new to appear on these lists too. http://www.chiro.org/nutrition/ABSTR...orticosteroids You might find d-ribose useful...I have a thread here on it as I have been using it for about 3 months. It gives a nice improvement in stamina-- http://neurotalk.psychcentral.com/sh...ghlight=ribose |
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