Orthodics advice
Oakley
8 years ago
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amj0517
8 years agoRelated Discussions
Morton's neuroma?
Comments (22)I know this post is 6 months old, but I would like to continue it. As I said above, I developed severe stinging toe pain several years ago. I should have gone to see my favorite podiatrist, but instead, went to a foot/ankle ortho doc who was in the same clinic as the doc who did my knee surgery. This doc took xrays and examined my foot and said he couldn't find anything wrong with it. I had sure thought it was a neuroma. He had me get custom orthotics that never helped and had me have physical therapy for awhile, which didn't help. It all seemed to get slowly better and I would just have stinging/numb toes intermittently over the past 2 years. Then, a month ago, I sprained my ankle and the limping brought this horrible pain back. I finally called my old podiatrist and traveled 50 miles to see him. Right away, he diagnosed a neuroma. He said I no doubt had this neuroma over 2 years ago when I saw the other doc. Anyhow......he gave me a steroid injection and said that he wasn't sure it would work, since it was so large, and I'd had it for so long. My 2nd and 3rd toe were even pushed apart because of it! It makes me soooooo angry at the ortho doc. And those docs always bad-mouth podiatrists. Anyhow.........more questions for those of you who have had this problem and had the steroid injection or the surgery: How long did you try to avoid walking on your foot after the injection? How long did it take to feel better? The doc said I could be on it a little tomorrow, but I sure want to maximize the chances of it working and will rest it as long as I need to. He said if this doesn't work, I will need surgery. But he said I would have to be off my feet completely for 1 week afterwards, then during the second week I couldn't be on them more than 3-4 hours at a time. That I would be in a surgical boot for 2 weeks. Wow. that seemed like alot of down time. I thought cutting the neuroma out would be easier than that. But he said if you irritate it too soon, it could form adhesions and scar tissue. I intend to write that ortho doc. Why would he overlook a neuroma, when I had the textbook symptoms????? He is at a major sports clinic in a big city. When I think of the money I wasted on him/orthotics/physical therapy, it makes me very angry. I should have followed my gut and traveled the distance necessary to see my podiatrist. I won't make that mistake again. Any info you might have will be appreciated!...See MoreCan you help me find an athletic shoe?
Comments (18)Kitchendetective, I feel your pain! It really is a shame that the nearest New Balance store is 80 miles away but, I'm going to have to add my voice to the "go to a New Balance store" recommendation. A couple of months ago I was in the same boat you are. My well used NB runners were falling apart and no matter what NB shoes I tried on nothing seemed to give me sufficient cushion. I finally broke down and went to a NB store. They have a machine that stand in (after removing your shoes) which will indicate on a screen just where the pressure points on your feet fall. Helps the NB folks determine exactly what kind of runners you need. Well, color me shocked. All my adult life I've *known* I have flat feet....except the machine showed that I really don't have flat feet. My wet footprints look that way becasue of the motion my feet go through when I'm walking. I not only needed a shoe with good cushion, I needed one that stabilized my foot. The guy who was helping me put exactly one shoe on me and it was like nothing else I'd ever had on my feet in my life. Yes, it felt that good. Yes, it was more than double the price that I usually paid for NB at Kohls or Shoe Carnival.....but I'm so glad that I did it! My feet feel "years younger"! I live in my runners and, as a dog trainer, they get a ton of abuse and use on a lot of different surfaces. When I find a pair I like, I generally buy 2-3 pairs. I didn't do that at the NB store since they were so pricey but, I came home and found exactly the same shoes at Online Shoes and ordered two additional pairs from them at a considerable saving. I suppose I could have returned the ones I bought at the NB store but as far as I was concerned the sales guy worked hard to ensure that I got shoes that worked for me so the extra cost was worth it. For one pair....See MoreChiropractic Feels Like. Scam??
Comments (30)Martinca; who else in your family has joint pain? What I pasted in below is the 1st sign that this will probably be life long. I'm not sure they will get a good handle on it. Hyper-mobility of the joints is called EDS- Ehlers Danlos Syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders, characterized by articular (joint) hypermobility, skin extensibility and tissue fragility. Ehlers-Danlos Syndrome (EDS) is a group of inherited disorders that affect connective tissue. Take a look at the link below; it opens the direct PDF location; you can either open or save it. Back around May; I made a post about Chiari Malformation for a friend. One of the gals here mentioned that she has EDS & little did I know that this would smack me in the face in another 6 weeks after my post. I had no clue what EDS even was; but I'm learning a lot & it's why I haven't been around much the last few months. My daughter has been majorly suffering for 3 years; guess what? Her mystery diagnosis will most likely be EDS. We saw the 1st neuro yesterday; have to find a geneticist probably endocrinologist & rheumatologist. People can live with varying degrees of EDS; some may never know they have it while others are wrongly diagnosed with fibromyalgia. Still others will be fine until like your grand daughter; injure themselves & do not heal right. There is no "test" to confirm EDS; from what I understand it goes off of symptoms which are many. How are her teeth? Please be careful with braces; from what I'm reading they actually weaken teeth- which fits in with my daughter & how her teeth are breaking at the gum. Another issue is she may not be able to be put down for surgeries. My daughter had a molar pulled a few weeks ago; they couldn't get the IV meds to knock her out. Back to her ankle; from what I do understand; the right physical therapist; possibly chiro may be able to work with her to strengthen it. I dislike the word cured because from what I'm reading with others diagnosed; she's going to have to keep working at it but with the correctly trained people. Send me an email; I'll get you set up at a decent facebook group. Inspire also has an EDS board. she is 13. She's had X-rays and MRI . We 've been told she has hyper- mobility of the ankle caused by weak ligaments , and perhaps exacerbated by an injury( sprain). Two months of pt and home exercises only caused more pain and no improvement. Here is a link that might be useful: So You Think You Might Have EDS?...See Moreanti fatigue mats or shoes/clogs
Comments (12)downsouth, Amidst all the foot recommendations, the gelmat recommendation got lost. A LOT of people have found that very useful in their kitchens for where they tend to stand and walk a lot, so go for it. I have contemporary spaces so have a cushioned chilewich mat instead which I also like both visually as well as for the warmth and comfort they provide. But I think the gelmat may be what your feet would best appreciate. On other piece of advice - even if it appears a non-sequiter. I had had just the same experience you had after our remodel although we didn't add tile floors in the kitchen or bath, just replaced the previous ones. Pain in the feet, difficulty standing, couldn't relive it. This is what I found - in my case, the problem was actually a behavioural one. I used to religious run and go for yoga classes twice a week. The remodeling phase was disruptive and I couldn't maintain my routine to the point that exercise had become quite sporadic and random - I ran when I could. After the remodel many months later, I ran but still tried to give the feet a break so not as much as before and tried to wait for the feet to improve before going for yoga (my doc ruled out Plantar fascitis and didn't find anything amiss). Well, eventually, a year and a half later, I decided that pride be damned, I was just going back to yoga and if I could only do 1/4 of the class, so be it. Guess what, we got into a particular sequence of poses and I knew immediately that I'd found the problem and literally I was 1000% better by the end of the class and after two of these classes had COMPLETELY resolved the foot-pain problem. Basically, my body needed the complete stretch it was so used to and giving my calves and hamstrings a thorough stretching was all hte relief my feet needed. Oftentimes problems manifest themselves at the end of a certain kinematic chain when the root problem is someplace else entirely. In general, I think wearing shoes around is a good thing - personally I'm not convinced that tile is harmful for its hardness - I have hardwood or tile ONLY in the house and I can assure you that my hardwood floors are no more compliant than are the tile (the bigger drawback to tile is the coldness and underfloor heating there makes the warm tile floors far more comfortable than the hardwood). The gelmats or cushioned mats are nice - period. Separately, getting an all-over exercise plan is critical (I keep telling myself this same thing but I'm a running junky and truthfully that is all I ever really want to do - no matter my resolutions to go to the gym to lift weights etc. but I need to start that up, too)....See Morellitm
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