Joined
·
14 Posts
<span style="font-family:Calibri;"><span style="font-size:medium;">I've been running on and off for 25 years. Never a foot problem. Three months ago I laced up my trail shoes for a 10 miler and after about 1/4 mile I felt like my sock was bunched up. Took my shoe off, to find it wasn't; repeated this again; then said screw it and just ran on it. Since then the sensation has come and gone. The last month it bothered me regularly, and sometimes would hurt when I walk. It feels like a ligament clicking in my third toe. Sometimes it feels like my fourth toe. I thought I was nuts not being able to tell which toe was injured. When I run, it bothers me for about a mile so I curl my toes to alleviate aggravating it for a while and it gets a little numb after a while. Now it bothers me most of the time, so I went to a Podiatrist to see what’s going on.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">So it turns out it’s not my toes, Pod says it’s a nerve in the ball of my foot. A neuroma or possibly neuritis. I had never heard of this before so I’ve done some research on it.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">The Pod said I'm only a moderate pronator and said orthotics might help but didn't stress them for me. He felt motion control shoes are adequate. I decided to order the orthotics anyway. I figure it might help and it probably won’t hurt.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">He had the nurse tape me (first a horse shoe shape around the outside of my foot from knuckle to heel to knuckle, then two loops kind of loose around my foot top to bottom). This was done to keep my foot from spreading out too far. He said no restrictions on running walking or whatever and come back in a week. He said the next progression would be cortisone injections, then possibly alcohol injections and then surgery, but that he felt we caught mine early and it might go away before the invasive stuff.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">I'm trying to figure out why this would suddenly affect me. No recent shoe changes. We did move into a house in April 2007 with hard wood floors and slate floors and I’ve gone barefoot a lot this summer. I wonder if this caused it. Maybe walking on the hard floors made my foot spread out like a pancake and pinch the nerve when I had my trail shoes on (they are a little, but not overly snug). It would have been 4 months after moving that I first felt the sensation. What’s remarkable to me, is the Pod doesn’t seem interested in what caused the neuroma. I’ve read that some people get it from being over pronators with musculoskeletal problems. Some people get it from wearing shoes that are too tight. I would think the approach to dealing with it would be different in these two cases. I’m convinced that mine is caused by either the sudden abundance of barefoot walking on hard floors this summer, and/or my trail shoes were too tight on a couple runs.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">I’ve read that most people with a neuroma seem to be comfortable barefoot, but when they get shoes on they hurt. I’m the opposite. If I go barefoot, I have to limp in order to prevent the pain. I feel better in shoes. I have to wear shoes at all time now.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">Common sense tells me I should get on crutches for a week or three and this should go away, but the pod says not necessary; live life normal. That’s hard to comprehend, but since I don't want to quit running, I'm following Dr’s orders.</span></span><br><br><span style="font-size:medium;"><span style="font-family:Calibri;">I went back to the POD last Tuesday and he gave me a cortisone injection. It made me numb for a day, then sore for a couple days, now it’s the way it was before the injection. CRAP! From my research, it seems no two Pods have the same opinion on the best method to tackle this. Some are against surgery. Some are against alcohol shots. Some do Cryo Surgery. Some recommend an MRI. Some say an MRI is a waste of time.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">I’m considering going right to surgery. Alcohol shots only cure 70% +/- of mild cases and the alcohol just kills the nerve anyway, so why not just cut it out? I don’t have insurance and don’t want to spend al the $$$ on stuff that isn’t going to just fix the problem.</span></span><br><br><span style="font-family:Calibri;"><span style="font-size:medium;">This sure is frustrating. Anybody else have experience with this?</span></span>