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02-02-2012, 07:19 PM | #1 | ||
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I had to go to the emergency ward at my local hospital, because I had so much pain in my right thigh, they told me to come back the next day for a ultra-sound, I had just come back from a trip and thought that I might have a blood clot in my leg. I did go back the next day and they told me I did not have a blood clot, and that it was probably just a pinched nerve, and not to worry. I have not slept for more than 3-4 hours a night in the last 1 1/2 weeks, I did some research, and I am convinced I have Meralgia paresthetica. Is there any Canadians on this board that are dealing with MP? The Canadaian health plan SUCKS!!! ( get ready Americans! it is going to get very UGLY) I know once I get to see my doctor it will be 6 months before I will get to see a specialist. Is there anything I can do myself to eleviate the pain ( beers not working ).
Rottonron |
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06-13-2013, 02:14 AM | #2 | ||
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04-30-2016, 11:53 PM | #3 | ||
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"Thanks for this!" says: | St George 2013 (05-02-2016) |
05-01-2016, 02:45 PM | #4 | ||
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Hi Mando,
Welcome to NT but so sorry to hear MP brought you to us. You are NOT alone but you may find this forum a bit inactive because many MP sufferers have it on a temporary basis. But then, there are a few of us that suffer with it for a lifetime. If you ever want to chat about it, feel free to contact me. Most of the people have come and gone but there are a few of us that remain. One of the posters that left due to recovery, kept in touch with me after they had their LFCN removed. It took at least 6 months before ALL symptoms were gone. I guess it is like when one has an amputation and phantom limb pain of the missing limb. The GOOD news, this person, has now totally recovered, is back to living a VERY full life and has resumed all the activities that MP had taken away. Since your decompression was recent, I would not give up hope just yet. What does your doc say? I know I would feel like the surgery was a failure if I still had pain after going through a decompression procedure, but based upon what I was told by others, and my own personal experiences (not with decompression or removal), some treatments do take time to produce the desired effects. We are here if you wish to keep in touch. Welcome aboard but again sorry to hear of your suffering. You are NOT alone. |
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"Thanks for this!" says: | St George 2013 (05-02-2016) |
08-23-2016, 01:04 PM | #5 | ||
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08-23-2016, 01:55 PM | #6 | |||
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I'd like to just add that Aspercreme is now making an OTC lidocaine patch. It is 4% however, whereas the RX Lidoderms are 5%.
But the Aspercreme ones are affordable. example: Aspercreme with Lidocaine Patch, 5CT - CVS.com I found with my years long severe MP, and daily use for 2 weeks put me into a remission. As long as I don't use heat on that leg/hip area, I stay in remission. Heat however triggers the nerve to fire again. So I rarely use my Lidoderms anymore. I never expected a remission of pain, but I guess it is possible for some people.
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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