| FAQ/Help |
| Calendar |
| Search |
| Today's Posts |
03-17-2008, 08:22 PM
|
#4 | ||
|
|||
|
Magnate
|
I know Roxie uses them for her back and finds them helpful. I have found them to increase my pain but I am weird. It is not from the meds inside but anything resting on my pain area even a finger aggrevates. As for the stick if you are just getting out of the shower or bath try to wait a little so your skin is not so wet still. The foot sounds hard if on the bottom. Could you put it on the top and may stick better?
|
||
|
 Reply With Quote
|
|
|
Similar Threads
|
||||
| Thread | Forum | |||
| Anybody using Lidocaine patches? | Spinal Disorders & Back Pain | |||
| Pain Patches | Thoracic Outlet Syndrome | |||
| Do you use Lidoderm patches for your RSD/ CRPS? Please tell me about your experience! | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
| Any Suggestions on how to keep Lidoderm patches attached... | Thoracic Outlet Syndrome | |||
| Any Suggestions on how to keep Lidoderm patches attached... | Spinal Disorders & Back Pain | |||
Threaded Mode