Another update - yes it's been a while, and here's why...

Hey Friends,
I know this site now gets a good amount of traffic from across the globe, and things have been a bit silent on my end.

Here's why: when your foot is healed properly, it stays healed, at least in my case. I follow all of the advice I share with others.

So, I typically have been going about my normal daily life as it relates to my foot and the MN. No pain, no issues, nothing. It's 100% healed. Unfortunately, though, I was in an accident which totaled my car (I was rear ended at a stop light while in my small Toyota ECHO and hit full speed by a guy in a four door F-150), and I have some significant issues in my back and right knee that I have been addressing. This has limited my workouts and even family/work life. One day, this too will pass!

Nonetheless, I want to make sure everyone knows that the plan I had implemented have worked as I had strategically hoped. I am still rocking my VFF and Vivobarefoot shoes and boots. I will never wear a conventional brand shoe again unless the follow suit with those two brands.

With that, have a great day, and enjoy the gifts you have.

Here's To Healing,
Shane

Vivobarefoot Evo Lite

Hey everyone,

Just wanted to share an update - I recently found an awesome deal on amazon and was able to snag these bad boys for about $60!  Retail is normally $130.  

As you know, my foot is doing awesome, and these Vivobarefoot Evo Lites are great for a couple reasons:

1. I can wear my Correct Toes in them (I still wear them because I believe it still helps my foot anatomy.  It took years to get jacked up, and it will probably take a year to get back to a true natural state).
2. They look great.  It's good to have footwear like this because it is also a great conversation starter if you want an ice breaker to help people realize they might be wearing expensive garbage for shoes.
3. They are zero-drop and they have wide toe boxes.  Very natural layout and design.  Big score there.

So, as you can imagine, if you happen to be in the market for good shoes, I still suggest the Altra brand, as well as Lems, but these Evo Lites are really sharp and they might be a great match for some of you.  You can read the reviews on amazon to determine your sizing.  I normally wear a U.S 12.5 or 13, and I ordered these in the 47, which is also what I wear for my Vibram Five Fingers.

Be well!

Blog Dedication & Disclaimer

Dear Visitors,
This blog is dedicated to people that have, or believe they have, a Morton's Neuroma.  It is also dedicated to keeping up to date with current victories and effective treatment plans for any types of symptom reversal.  As someone that currently has a MN in my left foot, my end goal is really for people to have a hub where there are more posts related to beating MN vs posts where people are complaining about it.  Make no mistake, MN is a pain in the foot, but also a huge pain in the butt.  And during my research, when I first started looking for help, most of what I came across online was blog sites related that just had thread after thread of complaining, but hardly any worth while posts or feeds about actually reversing the neuroma.  That's where this site comes in.  

And, I ask that you share this blog with your friends and family, regardless of age nor activity level.  As you'll read in the other pages, foot ailments and symptoms should really be avoidedat the root level - the footwear!  
   One thing I also want to point out is that I am a conservative/natural type of guy.  I am not sold on going straight to surgery or medication or orthotics right away.  I believe too many folks are getting pushed into the podiatrist factory line of "Oh, well, let's get an x-ray, and over to your right you will find some orthopedic shoes that we'll probably suggest for your orthotics."  I simply don't believe that is the best route for long term correction and restoration of the nerve.  

Disclaimer: I am not a doctor, and anything posted within this website is merely a breakdown of my own experience with my own MN, as well as information or products that I feel are worthy of sharing that I have discovered through hours of research since I started having pain and symptoms in early 2014.  As always, consult your physician before attempting to put into practice anything you read online, even if "it" has worked for someone else.  Especially since Morton's Neuroma symptoms can vary or be misdiagnosed on occasion.

Cheers! And here's to beating this thing with non-invasive, conservative and natural methods...