Guest guest Posted August 16, 2001 Report Share Posted August 16, 2001 Hi Connie: Great news. Thanks for posting. hugs, lea > Hi Everyone, > I have been on Lidocaine patches..........they are wonderful..........kind > of a gel patch.........you slap them right on what's hurting and change them > every 12 hours..............My back pain has subsided and so has the ankle > pain........even the swelling is gone....... > Certainly a prescription is needed..............but boy what a great > relief.........I love my Neurologist, I love my Neurologist.........and my > LLMD, she recommended the Neurologist..........I love them both..........for > the first time..........I really feel they are determined to get me feeling > well!!!!!!!!!! > ConnieK nwnj > > Leave no stone unturned.......and ask questions! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2006 Report Share Posted February 22, 2006 I tried them for my lower back...didn't seem to help. marysmith20022 <marysmith20022@...> wrote: Has anyone else tried the Lidocaine patches. Vivian Harkness http://www.geocities.com/southeastsearchandrescue/index.html --------------------------------- Use Photomail to share photos without annoying attachments. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 I used some sample patches (they stuck fine on my arm) but the insurance wouldn't pay for them. So the doctor prescribed the gel format " Lidocain Hydrochloride Jelly USP 2% " which they DO cover. It seems to be working just as well as the patch - been using for about 2 weeks now for Radial Tunnel Syndrome. -- Rhinehart Bassett (Pasadena CA) " Genealogy is my bag " " GH is my soap " kathryn@... http://bassett.net > Lidocaine patches > > Hi guys, > > I just got these yesterday at the doc to use in partnership > with pain meds and hopefully so I can cut back on the meds > since my liver is getting shot.anyway, it seemed to work for > a bit but it fell off - not too stick so I guess I will have > to get some tape. I thought I would let those of you who > have not used them try and those who have comment.I'm > interested to learn the experiences before I ask for a > complete prescription of them on top of the other - he gave > me a few samples.we will see. It did seem to help in the > joint areas that the drugs seem to not get all the pain from > and I know they use it in fibromylagia (sp) patients too. > > Thoughts? > > SFG Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 I was given the patches after my surgery to help with pain from scar tissue. They didn't work for me because I couldnt get them to stick even with tape.But I have heard people who liked them. Tim Bassett <kathryn@...> wrote: I used some sample patches (they stuck fine on my arm) but the insurance wouldn't pay for them. So the doctor prescribed the gel format "Lidocain Hydrochloride Jelly USP 2%" which they DO cover. It seems to be working just as well as the patch - been using for about 2 weeks now for Radial Tunnel Syndrome.-- Rhinehart Bassett (Pasadena CA)"Genealogy is my bag" "GH is my soap"kathrynbassett (DOT) nethttp://bassett.net > Lidocaine patches> > Hi guys,> > I just got these yesterday at the doc to use in partnership > with pain meds and hopefully so I can cut back on the meds > since my liver is getting shot.anyway, it seemed to work for > a bit but it fell off - not too stick so I guess I will have > to get some tape. I thought I would let those of you who > have not used them try and those who have comment.I'm > interested to learn the experiences before I ask for a > complete prescription of them on top of the other - he gave > me a few samples.we will see. It did seem to help in the > joint areas that the drugs seem to not get all the pain from > and I know they use it in fibromylagia (sp) patients too.> > Thoughts?> > SFG Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2007 Report Share Posted March 21, 2007 Yeah, these were 5% but had some effect but no sticking power so they didn’t last long…they are supposed to stick 12 hours – yeah right…, do you know what the gel percentage is – would it be 5% too? From: Spinal Stenosis Treatment [mailto:Spinal Stenosis Treatment ] On Behalf Of Tim West Sent: Tuesday, March 20, 2007 5:47 PM Spinal Stenosis Treatment Subject: RE: Lidocaine patches I was given the patches after my surgery to help with pain from scar tissue. They didn't work for me because I couldnt get them to stick even with tape.But I have heard people who liked them. Tim Bassett <kathrynbassett (DOT) net> wrote: I used some sample patches (they stuck fine on my arm) but the insurance wouldn't pay for them. So the doctor prescribed the gel format " Lidocain Hydrochloride Jelly USP 2% " which they DO cover. It seems to be working just as well as the patch - been using for about 2 weeks now for Radial Tunnel Syndrome. -- Rhinehart Bassett (Pasadena CA) " Genealogy is my bag " " GH is my soap " kathrynbassett (DOT) net http://bassett.net > Lidocaine patches > > Hi guys, > > I just got these yesterday at the doc to use in partnership > with pain meds and hopefully so I can cut back on the meds > since my liver is getting shot.anyway, it seemed to work for > a bit but it fell off - not too stick so I guess I will have > to get some tape. I thought I would let those of you who > have not used them try and those who have comment.I'm > interested to learn the experiences before I ask for a > complete prescription of them on top of the other - he gave > me a few samples.we will see. It did seem to help in the > joint areas that the drugs seem to not get all the pain from > and I know they use it in fibromylagia (sp) patients too. > > Thoughts? > > SFG Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2007 Report Share Posted March 21, 2007 As I stated, " Lidocain Hydrochloride Jelly USP 2% " . It seems to be as effective as the 5% patch, I'm guessing because the gel goes into the skin, whereas the patch lays on the skin so probably needs a larger percentage. My rx for the gel is 3x/day. > Lidocaine patches > > > > Hi guys, > > > > I just got these yesterday at the doc to use in partnership > > with pain meds and hopefully so I can cut back on the meds > > since my liver is getting shot.anyway, it seemed to work for > > a bit but it fell off - not too stick so I guess I will have > > to get some tape. I thought I would let those of you who > > have not used them try and those who have comment.I'm > > interested to learn the experiences before I ask for a > > complete prescription of them on top of the other - he gave > > me a few samples.we will see. It did seem to help in the > > joint areas that the drugs seem to not get all the pain from > > and I know they use it in fibromylagia (sp) patients too. > > > > Thoughts? > > > > SFG > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2007 Report Share Posted March 21, 2007 Thanks – I was curious what to ask for and how it would be different and you answered it for me – thanks again! It probably is easier to get around the knee and ankle areas too since my spine and joints are the worst. From: Spinal Stenosis Treatment [mailto:Spinal Stenosis Treatment ] On Behalf Of Bassett Sent: Wednesday, March 21, 2007 5:18 PM To: Spinal Stenosis Treatment Subject: RE: Lidocaine patches As I stated, " Lidocain Hydrochloride Jelly USP 2% " . It seems to be as effective as the 5% patch, I'm guessing because the gel goes into the skin, whereas the patch lays on the skin so probably needs a larger percentage. My rx for the gel is 3x/day. > Lidocaine patches > > > > Hi guys, > > > > I just got these yesterday at the doc to use in partnership > > with pain meds and hopefully so I can cut back on the meds > > since my liver is getting shot.anyway, it seemed to work for > > a bit but it fell off - not too stick so I guess I will have > > to get some tape. I thought I would let those of you who > > have not used them try and those who have comment.I'm > > interested to learn the experiences before I ask for a > > complete prescription of them on top of the other - he gave > > me a few samples.we will see. It did seem to help in the > > joint areas that the drugs seem to not get all the pain from > > and I know they use it in fibromylagia (sp) patients too. > > > > Thoughts? > > > > SFG > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2009 Report Share Posted September 16, 2009 , pain patches aren't the way to treat your body. You need to get over the stubborn phase and 'give in' to the right meds that will fix some of your problems. As time goes along, damage continues and won't fix themselves. Doctors and medical knowledge weren't just happenings, they were made to help us.If you don't want to be treated, why did you go to the Rheumy to begin with? Dennis in eastexas On Wed, Sep 16, 2009 at 9:39 AM, musiclvr3237 <musiclvr3237@...>wrote: > > > > Good morning everyone, > > Long story, short version. Rheumatologist appointment yesterday 3:45. > Weighed in, > Blood pressure 124/81. Temperature 98. Verification of prescriptions I > am on, Humira and Aleve. Did not have chest xray taken. Was seen by > doctor at 4:00. Yep....still have RA. Yep...still stubborn. Won't > take plaqunil, arava, methotrexate, prednisone, nor cortisone > injections. What are we going to do with you she asks. Was prescribed > Tramadol / Ultram and was given Lidoderm (Lidocaine patches). Was > prescribed Tramadol in February, 2007. Can't remember why I stopped but > I have half a bottle left that says discard after 3/07. Picking up > Humira and Tramadol this afternoon. > Told doctor having most pain, discomfort, and problems with C7 (the most > prominent > vertebrae at the base of the neck). She told me to cut the patches in > quarters and place a patch on the area for 12 hours on and 12 hours off. > Put my first patch on at 6:00 last night and took if off this morning > when I got up. I can't remember the last time that area felt so good. > Wish I could wear patches everywhere and always. Don't think I want to > go 12 hours without one now, but I am, and I hurt. I'm going to do more > research now on these patches. Hope you all have a great day. > Take care, > (musiclvr3237) > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2009 Report Share Posted September 18, 2009 Dennis, You are absolutely right....pain patches are not the way to treat a body. I tried just that one and am now scared to try another because of how I felt when I didn't have the patch on. I also did some reading on it and don't really want to toxify by body. Tried the Tramadol yesterday. Took one in the morning around 9. Thought it worked good as the pain in my neck, shoulders, and head didn't seem so intense and constant. Took a second pill around 6 pm right before dinner, and it knocked me out! I could not keep my eyes open. I think I know now why I stopped taking them before. So....I don't know. Stubborn does what stubborn is....would I rather be drugged, in no pain, and asleep, but missing out on life....helping my son with his homework, making dinner, and spending time with others.....or not take that pill, be in constant pain but deal with it, and try to live my life the way I've pretty much known it with RA for the last 18 years. Doctors, you are absoultely right, are here to help us.....but the drugs....nah....not so much. I was seen by my first rheumatologist in 1991 because I could not move, and I could not lay still...without being in excrutiating pain....if that makes any sense....I was given cortisone shots each month for almost 6 months in alternate shoulders. I was put on feldene, then prednisone, then methotrexate, then since nothing was working, he wanted to put me on gold shots and / or gold pills. Lost insurance. Couldn't get other insurance because of pre-existing. blah, blah, blah.... Was seen by the same rheumatologist 14 years later in 2005 after being granted Medicaid insurance. I also applied for disability benefits. He started me on Remicaide and some kind of electro-shock treatment in my shoulders. I had two infusions of Remicaide and lost my Medicaid insurance. Thought I was going to die. Was granted disability in March 2008 and began seeing my current rheumatologist. So yes, Dennis, part of me does want to be treated, but the other part has always wanted to be cured. (musiclvr3237) From: Dennis W <betnden@...> Subject: Re: [ ] Lidocaine Patches Date: Wednesday, September 16, 2009, 1:20 PM , pain patches aren't the way to treat your body. You need to get over the stubborn phase and 'give in' to the right meds that will fix some of your problems. As time goes along, damage continues and won't fix themselves. Doctors and medical knowledge weren't just happenings, they were made to help us.If you don't want to be treated, why did you go to the Rheumy to begin with? Dennis in eastexas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2009 Report Share Posted September 18, 2009 , If I may ask, could you tell me a little more about the electro-shock treatment for your shoulders? did it help? I agree with both your point of view as well as Dennis'. For me at least, I believe in having the best quality of life that you can make for yourself. For me, if I am in a flare, if I can get a good night sleep that is as pain free as possible and that may mean taking a pain pill, I have found that getting that good nights sleep enables me to struggle easier thru the day w/out pain pills. I do agree that no one wants to be in a drug induced " fog " during the day because you become useless. There is a fine line that each of us must tweek so that we can be somewhat comfortable as well as functionable in our lives. It's enough that the drugs we MUST take for the RA are poisonous to our bodies. in SC From: Dennis W <betndengmail (DOT) com> Subject: Re: [ ] Lidocaine Patches @gro ups.com Date: Wednesday, September 16, 2009, 1:20 PM , pain patches aren't the way to treat your body. You need to get over the stubborn phase and 'give in' to the right meds that will fix some of your problems. As time goes along, damage continues and won't fix themselves. Doctors and medical knowledge weren't just happenings, they were made to help us.If you don't want to be treated, why did you go to the Rheumy to begin with? Dennis in eastexas Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2009 Report Share Posted September 18, 2009 I agree about the lidocaine patches, they just numb the area giving you a false sense of well-being, masking the damage occuring by weight-bearing and movement and stuff. If anything, try the Flector Patches if you can, they have NSAIDS in them, you apply to the spot that hurts and they reduce the inflammation (the real devil). Some people cannot use them though. I do know they work great for me. We joke about RA in my house (they call it RA Puff N Stuff, The Lucifer Chronicles, they say the Stay-puffed marshmallow man is my real dad) Well u gotta laff sometimes. OKD Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2009 Report Share Posted September 18, 2009 " The Lucifer Chronicles " ....hee, hee, hee!! ~Connie From: OKD <Cofade_2000@...> Subject: [ ] Re: Lidocaine Patches Date: Friday, September 18, 2009, 10:15 AM I agree about the lidocaine patches, they just numb the area giving you a false sense of well-being, masking the damage occuring by weight-bearing and movement and stuff. If anything, try the Flector Patches if you can, they have NSAIDS in them, you apply to the spot that hurts and they reduce the inflammation (the real devil). Some people cannot use them though. I do know they work great for me. We joke about RA in my house (they call it RA Puff N Stuff, The Lucifer Chronicles, they say the Stay-puffed marshmallow man is my real dad) Well u gotta laff sometimes. OKD Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2009 Report Share Posted September 18, 2009 I have tried lidocaine and Flector, not success with either. > > I agree about the lidocaine patches, they just numb the area giving you a false sense of well-being, masking the damage occuring by weight-bearing and movement and stuff. > > If anything, try the Flector Patches if you can, they have NSAIDS in them, you apply to the spot that hurts and they reduce the inflammation (the real devil). Some people cannot use them though. I do know they work great for me. > Quote Link to comment Share on other sites More sharing options...
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