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Spinal Disorders & Back Pain For discussion of all spinal cord injuries, spinal issues, back-related pain or problems. |
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#1 | |||
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Member
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Hello everyone
I've been reading posts here for awhile. I want to first explain my situation. I have over 10 things "wrong with me", though not all of them are as serious as other. Here is my list of what I have been diagnosed with: polyneuropathy (small and large fiber), postural orthostatic tachycardia syndrome (POTS) degenerative disc disease, disc desiccation, arthritis, PCOS, allergies, migraines, and other medical problems and challenges, including only one good kidney. I am obviously not asking for medical advice as I would from a doctor. I'm not wondering about medications.. but rather other homeopathic type treatments that you have found to work for your pain. I am on the Fentanyl patch, which helps a bit with my neuropathy. However, my back pain is not being helped at all. I used to get relief from a heating pad on my back--that is the only thing that I have ever found that helps. Now, because I am on the patch, I am unable to use the heating pad. I cannot stand to use ice on my back. I also am bedridden and am unable to move around much. So I'm wondering what other things have helped those of you with back pain. I do as much stretching/exercising as I can from bed. Heat and ice are both out, and my TENS unit doesn't help me anymore. Does anyone else have any ideas that may help reduce the pain? Thanks! ![]()
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. ♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥ My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems. |
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#2 | |||
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Co-Administrator
Community Support Team
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Some possible alternative care ideas that you might want to look in to.
I don't know if you have explored any of these yet or not.. and I can't say positively if they will help any of your conditions or not. Magnets/ near/far infrared/ low level laser Hypnosis/meditation/EFT -types acupuncture /acupressure traction? for the spine? What is the most bothersome- the back pain? I hope you have a good quality mattress and plenty of pillows to help support and change positions when spending much time in bed. Pete Egoscue {lib books & website} has some simple positions that might help - http://www.egoscue.com/ his site isn't loading right now but here's another with some inf- http://www.shareguide.com/Egoscue.html
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Search the NeuroTalk forums - . |
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#3 | |||
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Wisest Elder Ever
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Can't use magnets when you get the SCS...
But using them now might really show improvement. They can stop overfiring nerves, however.
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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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"Thanks for this!" says: | Rrae (09-20-2010) |
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#4 | |||
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Member
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Thank you both for your replies.
Can you tell me what type of magnets you are talking about--I have never heard of using magnets for pain relief. I can look it up, if you can just give me a hint on what to search for.. magnets and pain relief? I will try that I guess until/unless I hear from someone on that. I don't see how magnets can affect pain, but I suppose anything is possible... That's why I wrote this--so many people have all these neat tricks and things that help them! Accupuncture isn't an option right now because I don't have money and my insurance doesn't cover it... but I have thought of it before. I may be able to try it in the future if I can get some income. I do have a good mattress, so that is helpful. I imagine that my pain would be magnified a lot more if I was sleeping on the mattress in my mom's room--it hurts my back a lot... especially being in bed the majority of the day. I am not sure what you mean, Jomar, by "hypnosis/meditation/EFT" and "traction? for the spine?" I do know waht hypnosis and meditation are, but have no idea if it is something that someone can do without the help of another person. When I am feeling a bit better, I will do some research and see what I can find out. I will also come back to this thread and look at the website with the positions on it. It does help to change positions, but my feet/legs don't tolerate much. The majority of the day I have to be flat on my back with a pillow under my feet/part of my legs. I can't lay on my side or my stomach and can't sit up in bed. I think that would help a lot, but my body just can't seem to handle it for very long. I do sit up when I eat meals usually, so I can tolerate a little bit--but not much. Thanks again for your replies. I will do some more research later.. I appreciate your help! ![]()
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. ♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥ My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems. |
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#5 | |||
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Wisest Elder Ever
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Please read this thread carefully and consider.
http://neurotalk.psychcentral.com/thread118248.html These are very strong now, improved. One or two (at most) for an hour a day...may just work for you. For more severe pain, longer may be necessary at first. I find 20-30 minutes now good for most problems. Red side toward the body..you can use surgical tape. Placement is important, so figure out where you need to put them. The link I give shows nerve distributions, to help you. You also have your medical reports detailing areas that are problematic so use those. I find it odd that your fentanyl is not working for you. It should.
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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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#6 | ||
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Member
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Things that I have found very useful are remedial massage, magnesium oil, and Vitamin D.
My main treatment until recently was regular massages. For the last 3 1/2 months I haven't needed massages as the magnesium and Vit D have now removed the muscle tightness, pain, and headaches. I take 5000 B units 3 times a week, after a test revealed I was a bit low, and 2 teaspoons of the oil daily, diluted in water. Well worth a try.
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See my mosaics . . |
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"Thanks for this!" says: | smae (09-21-2010) |
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#7 | |||
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Member
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mrsD,
That link was very helpful.. thanks. As soon as I get some money, I hope to try the magnets. The fentanyl patch is working for my PN, it just doesn't do anything for my back pain... but it is reducing the PN pain and for that I am incredibly grateful. ![]() Quote:
__________________
. ♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥ My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems. |
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#8 | |||
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Co-Administrator
Community Support Team
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I wasn't sure if traction for the DDD is OK or not.
If some of the back pain is from the disks crowding or collapsing on things then traction {it's a gentle pulling/stretching to open up the spaces} might help, but it would be something to ask dr about and read more about it. ["hypnosis/meditation/EFT"] might help with addressing the emotional/mental side of chronic pain All of these have various videos on Google vids & you tube - some will be good and some will be not so good - so explore and find some good ones to try. EFT is this - http://www.eftuniverse.com/ you can sign up for a free starter download - there are lots of videos on that site also.
__________________
Search the NeuroTalk forums - . |
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"Thanks for this!" says: | smae (09-21-2010) |
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#9 | |||
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Junior Member
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I have had back problems all of my life; now entering my early 50's. Car accident in 2006 allowed me to get regular massage and hot/cold packs for about 6 weeks treatment from a trained specialist.
Here is the easy way: get anyone to use their fingertips and then the palm alternately all over your back, neck and buttocks. You will be amazed what the "Human Touch" can do to help your problem. No training required, just use a little common sense to let "the fingers do the walking". Mike |
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#10 | ||
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Junior Member
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Sarah Mae,
Re the fentanyl patch, may I ask how much you are taking? I'm on the patch for my PN and take 125 mcg every 72 hours. It helps but I'd like to ask my neurologist to bump me up to 150 ev ery 72 hrs. I'm wondering how others tolerate arious dosages. I'm fine with the 125 (100 mcg. on day one then an extra 25 during day three, since the patch seems to lose strength by day three. Thanks. Augie Quote:
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