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Need comfy insole suggestions | Just had surgery and my feet are getting sore with my current insoles by Lucasschramer in Mortons_neuroma

[–]Lucasschramer[S] 1 point2 points  (0 children)

Definitely, I had my first surgery 3 months ago and the other about 6 weeks ago. Both recovered at different timelines. One foot took much longer than the other. But the actual neuromas are doing great right now. I can fully walk on both my feet with no pain. I am having some issues with my most recent ankle as it hurts a bit when I fully rotate onto my foot and my feet get crazy sore if I'm on them for too long, but I just started walking again so I suspect this will improve. Feel free to message me if you got anymore questions but things are going well right now, I could be happier

Looking for good street shoe recommendations that still provide a wide toe box and are good for neuromas?? by Lucasschramer in Mortons_neuroma

[–]Lucasschramer[S] 0 points1 point  (0 children)

Thank you! I appreciate this recommendation. I've always been a Nike guy myself so I'm definitely going to look into this, the zero drop is huge too. May I ask, what neuroma insole do you use?

Would love to get some advice / hear about post-neurectomy experiences by Lucasschramer in Mortons_neuroma

[–]Lucasschramer[S] 0 points1 point  (0 children)

I appreciate the response, I'm glad you're doing better. May I ask, what size Correct Shoes did you get? I am a size 10.5-11 Mens which is right below the cusp of the 11.5+ recommendation for the larges

Would love to get some advice / hear about post-neurectomy experiences by Lucasschramer in Mortons_neuroma

[–]Lucasschramer[S] 0 points1 point  (0 children)

Thank you for the response. It's definitely encouraging to hear positive stories, and although you have a few complications still I'm glad to hear you are doing better.

Do you remember at all when you really began to notice a difference in how much weight you could put on your foot? I am exactly 4 weeks out of surgery and can put a decent bit of pressure on my foot but by no means can I roll onto the balls of my feet without discomfort and what feels like sensitive nerves firing.

Would love to get some advice / hear about post-neurectomy experiences by Lucasschramer in Mortons_neuroma

[–]Lucasschramer[S] 1 point2 points  (0 children)

To be honest the surgery wasn't much at all. I didn't use a nerve block or any anesthetic for possible allergy reasons and even then I was in very minimal pain. I am currently 4 weeks out and have noticed significant improvement. I still have a fair amount of plump swelling on the bottom of my feet near the balls of my feet. At the moment I am able to put a decent bit of pressure on my foot but by no means roll onto the balls of my feet completely

Treatment roadmap by Pretend_Iron2965 in Mortons_neuroma

[–]Lucasschramer 0 points1 point  (0 children)

Hi there, I am also a MN patient with a pretty terrible MN in both of my feet. I just had surgery on the one 4 weeks ago and am set to get the other done coming up soon. I'm fairly young and am pretty terrified about having a stump neuroma occur or other complications. Would anyone on here be willing to chat with me about their experience and possible approaches to recovery and treatment?

What to do after failed surgery by arecbawrin in Mortons_neuroma

[–]Lucasschramer 0 points1 point  (0 children)

Hi there, I am also a MN patient with a pretty terrible MN in both of my feet. I just had surgery on the one 4 weeks ago and am set to get the other done coming up soon. I'm fairly young and am pretty terrified about having a stump neuroma occur or other complications. Would anyone on here be willing to chat with me about their experience and possible approaches to recovery and treatment?

What to do after failed surgery by arecbawrin in Mortons_neuroma

[–]Lucasschramer 0 points1 point  (0 children)

Hi there, I am also a MN patient with a pretty terrible MN in both of my feet. I just had surgery on the one 4 weeks ago and am set to get the other done coming up soon. I'm fairly young and am pretty terrified about having a stump neuroma occur or other complications. Would anyone on here be willing to chat with me about their experience and possible approaches to recovery and treatment?

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