Chronic Pain Support Group
Physicians and professionalsdefine pain as chronic if it lasts longer than three to six months and is persistent. It's distinct from acute pain that is a direct result of injury or trauma. This support group is dedicated to those suffering from chronic pain. Discuss treatments that have worked for you, find advice for your specific experience, and find support. You're not...
ConoIpsaro
Hi Everyone,
I am up late again with pain and burning in my feet as so often happens anymore. I have been having foot problems
that started back around 2006 sometime after I had a fragmented disc removed from L4/L5 area. The surgery went well and eliminated the back pain I had been suffering with for 15 years. I went to PT with a couple guys that are specialist in Spine and Sports rehab. They taught me exercises for the core that I was never aware of. Since then I continued to utilize the things they taught me. Life was good, I was able to continue being active mostly by bicycling long distances and taking long walks when the weather wasn't conducive to biking. Continued to do ab work religiously. Like I said, sometime after the surgery probably within a year or two I noticed that during the cold months of the year (november to March) my feet would always feel like there were marbles under my toes and like my socks were bunched under my feet. In the last three years its been more on then off. Got to a point where in 2011 I decided to see a Podiatrist who said I had signs of Neuropathy but never did a test. He recommended conservative treatment, Icing etc etc.. Later on in the summer of 2012 I went to see a Orthopedic foot doctor who recommended foot inserts and icing also. This never helped either so I went back to see him. He performed a very painful EMG nerve conduction study that indicated that there was nothing wrong. I started physical therapy. In the meantime I went back to the Orthopedic surgeon who operated on my back to see if any of this was related to the operation. He suggest PT which I started again with the guys from S&S. They informed me that over the years my foot has not formed correctly and that there was to much of a load being placed on the front portion of the foot. Soon after starting the PT I developed sever pain in the bottom of my left foot. This was sever enough to prevent me from walking for any distance or time. I was very limited because of the limp. I couldn't wear shoes and started wearing clogs on a regular basis to lighten the load. Eventullaly I went back to the foot doctor who after performing a MRI told me I have capsulitus of the second Metarsal. To help with this he suggested wearing a boot and staying off if for awhile. Well that didn't work out so well. By putting all the weight on the right side I developed sever sciatic pain. I finally went to see a second Ortho doctor for a second opinion because I thought the pain and burning that I have all the time was from the capsulititus. He indicated that it was not and that I PROBABLY have Neuopathy. Its frustrating for them to tell me this when all indications from the EMG say I don't have nerve damage. Also I am not diabetic and in very good shape. Recently I completed a 48 week treatment of three meds for Hep C which would probably be something that might enhance any previous symptoms for things such as Arthritus. The treatment went well as am now testing negative for the virus that has been with me for then 22 years. I had the foot problem before the treatment and continue to have it as of this writing. I am currtently taking Neurotin and have increased my intake of Vitaman b in hopes to aleviate the pain. Its always most painful at night when laying down. I still have a hard time wearing shoes because the numbness and feeling on the balls of my feet. I thoguht since the people I met on DS Hep C support group were so helpful that I would check this out to see if someone could enlighten me on some possible suggestions and/or remedies.... Sorry to be so long winded but I can't sleep and have nothing else to do or complain about. Wishing you all the best and stay warm where ever you are
I am up late again with pain and burning in my feet as so often happens anymore. I have been having foot problems
that started back around 2006 sometime after I had a fragmented disc removed from L4/L5 area. The surgery went well and eliminated the back pain I had been suffering with for 15 years. I went to PT with a couple guys that are specialist in Spine and Sports rehab. They taught me exercises for the core that I was never aware of. Since then I continued to utilize the things they taught me. Life was good, I was able to continue being active mostly by bicycling long distances and taking long walks when the weather wasn't conducive to biking. Continued to do ab work religiously. Like I said, sometime after the surgery probably within a year or two I noticed that during the cold months of the year (november to March) my feet would always feel like there were marbles under my toes and like my socks were bunched under my feet. In the last three years its been more on then off. Got to a point where in 2011 I decided to see a Podiatrist who said I had signs of Neuropathy but never did a test. He recommended conservative treatment, Icing etc etc.. Later on in the summer of 2012 I went to see a Orthopedic foot doctor who recommended foot inserts and icing also. This never helped either so I went back to see him. He performed a very painful EMG nerve conduction study that indicated that there was nothing wrong. I started physical therapy. In the meantime I went back to the Orthopedic surgeon who operated on my back to see if any of this was related to the operation. He suggest PT which I started again with the guys from S&S. They informed me that over the years my foot has not formed correctly and that there was to much of a load being placed on the front portion of the foot. Soon after starting the PT I developed sever pain in the bottom of my left foot. This was sever enough to prevent me from walking for any distance or time. I was very limited because of the limp. I couldn't wear shoes and started wearing clogs on a regular basis to lighten the load. Eventullaly I went back to the foot doctor who after performing a MRI told me I have capsulitus of the second Metarsal. To help with this he suggested wearing a boot and staying off if for awhile. Well that didn't work out so well. By putting all the weight on the right side I developed sever sciatic pain. I finally went to see a second Ortho doctor for a second opinion because I thought the pain and burning that I have all the time was from the capsulititus. He indicated that it was not and that I PROBABLY have Neuopathy. Its frustrating for them to tell me this when all indications from the EMG say I don't have nerve damage. Also I am not diabetic and in very good shape. Recently I completed a 48 week treatment of three meds for Hep C which would probably be something that might enhance any previous symptoms for things such as Arthritus. The treatment went well as am now testing negative for the virus that has been with me for then 22 years. I had the foot problem before the treatment and continue to have it as of this writing. I am currtently taking Neurotin and have increased my intake of Vitaman b in hopes to aleviate the pain. Its always most painful at night when laying down. I still have a hard time wearing shoes because the numbness and feeling on the balls of my feet. I thoguht since the people I met on DS Hep C support group were so helpful that I would check this out to see if someone could enlighten me on some possible suggestions and/or remedies.... Sorry to be so long winded but I can't sleep and have nothing else to do or complain about. Wishing you all the best and stay warm where ever you are
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I am not really familiar with foot problems. Hopefully someone else will come along that has more insight for you. Has the Neurontin helped you? If not, I know some people here have had success with Lyrica for Neuropathy.
Congratulations with testing negative for Hepatitis C!
I have peripheral neuropathy from lupus and found I had better results from Lyrica than Neurontin. I've been on it since it came on the market and now take the max dose of 600mg/day. But I also have fibromyalgia and RSD, so it helps all of it a great deal.
Also,I've found that keeping me feet warm at all cost helps the pain. I use my electric blanket even in the summer and wear socks all the time. No more bare feet for me!
Your PT tale gives me hope. I want to start back at the gym and want to strengthen my core. I don't currently have back problems (except a compression fracture in my L-Spine and the fibro) but I don't want to develop any problems in the future. I can use all the machines except for the leg ones. So I'll be superwoman on top and a gimp on the bottom. That works!
Lots of people here have peripheral neuropathy from lots of causes. I'm sure you'll find the help you need here.
Sandy
I was wondering if your doctors have ruled out other causes of neuropathy such as decreased arterial supply to the feet and diabetes?
Some people with high cholesterol suffer from micro vascular disease. Blood flow to the feet can be measured with a non-invasive test called Pulse Volume Recording.
Sometimes venous insufficiency can create pooling of fluid in the legs and press on small vessels, muscles and other tissues and cause foot discomfort.
Hope you will feel better soon
Beth
Onto your foot. I have Hueters Neuroma and exerienced the pain you are describing. Felt like I was walking on marbles, PT etc. My podiatrist prescribed orthotics and prednisone injections between my toes...OUCH! I was to receive two more 3 weeks apart and to start wearing my orthotics. I started with wearing them with the tennis shoes that have the rocker bottom and huge soles made of very soft rubber. Sketchers brand. They took awhile to get used to and I thought nothing woule ever work. Slowly with the orthotics, prednisone shots between my toes and the tennis shoe, I can say it has been 2 years and my foot is pain free. I never buy a pair of shoes without letting my orthotics into.
This was my experience and thought I'd share.
Welcome to this group and I am now on Gabapentin due to some unknown nerve condition affecting me from the neck down.
Welcome also to having a negative for HepC.
Joanne
Does it hurt to stand and roll your feet on a rolling pin or soda can so that your weight is on your arches? Does it feel better to go barefoot? Try wrapping your feet snugly in ace bandages. Any difference? You're basically going to have to be your own doctor on this. Try anything you can think of, and google your symptoms. Hopefully your research will lead you to an answer. Then you can clue your doctor in and then maybe he can help you.
Prayers going up for you.
breaking it like I just did makes it much easier to read long posts...
welcome and I am just suggesting a trick as I know others have issues with that type of posting too....look back at your post....is it easy to read? I know it is easier to write it....but think of others....
hugs bill
nice to meet ya
Hope you get answers.
Everyone has such different injuries and experiences. I have recently been in a car wreck and have injured my lower back. It is causing My feet pain, burning, sometimes like hot coals, sometimes like shooting knives, sometimes like I am walking on rocks. Mine is all from herniated disc in my lower back.
Just one more thought for you to look into. You have been given a lot to check into. Someone said you have to almost be your own doctor. That I have to agree on. Many times you have to do the research and take it to your doctor.
Hope you find answers soon. -RJ