Does anyone find that a type of shoe helps your foot neuropathy?
I am on a constant quest for shoes that don't kill my feet due to the neuropathy. I find that Spencos and Wolky shoes seem the best. Are there any other suggestions? Shoes can be just crippling for me. Horrid.
Interested in more discussions like this? Go to the Neuropathy Support Group.
I contribute my neuropathy to vitamin B-12 deficiency, which none of my doctors have considered. I was put on B-12 injections once a month back in the mid-1990s, but much too late as nerve damage was already done. My neuropathy has slowed and is progressing ever so slightly. It is my theory that I need a B-12 injection twice a month, but my primary care doctor will not entertain it. I still have a geographic tongue which is a symptom of B-12 deficiency and in my research geographic tongue will disappear once sufficient B-12 is present in my body. Logic would tell any doctor that trying B-12 injections every two weeks for a trial period of eight weeks or more to see if the geographic tongue would disappear would be a no-brainer. Maybe this will
benefit someone out there that may be experiencing my same issues.
Wondering if anyone else needs leather shoes in the winter? I cannot even find "Pleather", only mesh. Any ideas?
Sketchers does make leather shoes in men's but not sure about women's shoes. One member mentioned Xero shoes with a flat bottom which I've been looking at but the one I want for Winter is only in black and I want brown 😁
Saucony, "PWR Run", with a double thick Dr. Scholl insert. 1/2 or full size up, so plenty of wriggle room, and thick wool or alpaca socks.
I wear Crocs. I have some really pretty ones in bright colors!
Just wondering what this discussion has to do with the question asked?
Yes, Altra. Told to get a half size larger than my Merrill’s. These shoes have no slope and are designed with a LARGE toe box. Huge difference.
SAS shoes are high quality leather with heavily padded insoles. I add Dr. Scholl's gel inserts on top of the insoles.
Hi @chiefd67.
I am surprised that "none of your doctors have considered" vitamin B-12 deficiency as the cause of your PN. The tests to make this diagnosis are simple. Fortunately, vitamin B-12 deficiency is one of the easier causes to treat.
The first test to do is a vitamin B-12 level. The normal range is large, and some feel that a low normal result, especially in older people, may warrant treatment, or further testing. If the screening test is positive, the next tests would be homocysteine levels and methylmelonic acid. If one or both are abnormal, this probably makes the diagnosis, and would require treatment. Other tests could be a complete blood count, which may show a form of anemia called megaloblastic anemia.
It should not be necessary to take vitamin B-12 shots. There is a form of oral vitamin B-12 called methylated B-12 which is well absorbed.
Or, if you are mainly concerned with your tongue, you can simply take the methylated B-12, and see if your symptoms get better
Ask your doctor.
Thanks, I will request my primary care physician conduct the tests.