My book in finally here and ready for order!

I will cut to the chase - my book has finally been published! You can buy it here on Amazon. Click here for the direct page.

As I had mentioned in my last post, with the book now being online, and most of my content now being on our Facebook page, this blog will no longer be updated. I suggest you Like our Facebook page and follow updates there.

To those around the globe that have had to deal with Morton's Neuroma, there is hope, so don't give in. I am proof that it can be healed without surgery and all types of other non-sense that might be thrown at you. Always listen to the doctors, but never feel pressured or cornered; it's your body and you need to be able to live with whatever choice you make.

Be blessed,
Shane

Ugly, ugly pride

So, I felt like sharing this, because as I have pointed out, most of the public just goes along with just about any doctor's advice without doing ANY research on root causes, natural remedies, or alternatives toward restoration.

The other day my wife was at work, and a woman was walking with a limp and she and my wife started talking.  Turns out the lady has a Morton's Neuroma.  
So, my wife, who is super approachable, starts to mention how I HAD one, and how I healed it going the route of getting out of conventional shoes, going zero-drop, and also walking barefoot whenever I can.  The lady immediately starts to go down the road of, "Well, my foot doctor is one of the top doctors in the nation, and he said I should NEVER walk barefoot."  And my wife patiently tried to give some explanation as to why being barefoot can help splay the toes naturally and relieve the stress and pressure against the neuroma.  She just wouldn't listen.  Pride is a killer.

My guess is, based on my research and experience, that she is going to probably get the resection, and will likely be similar to many people that either get the stump growth and pain, or end up losing mobility of the foot...among other possibilities.  It pains me to say that, because there is a better way.  

Stay vigilant, and stay humble!  

Onward,
Shane

Merry Christmas, and Happy New Year!

Hi Everyone,

Just wanted to say thanks for reading and hopping on this blog.  I really hope it has been of some encouragement for you or someone you know that might be dealing with Morton's Neuroma.  It's such a pain, but I believe many people can get the solution they need by following some of the advice I have listed throughout this blog, whether from my own experiences or the professionals named or products/procedures listed.  I'm MN free, and I think tons of people out there can be restored without surgery.

Anyway, as we enter into Christmas and a New Year, I just wanted to wish you all an amazing time during your celebrations with friends, family, churches, companies, schools, etc.  Hopefully none of you end up with the Jelly of the Month Club memberships, but if you do, make the most of it!  

Bless you all,

Shane

Since I get emails on this topic...

Hey Friends,
So, I was noticing that I tend to get certain questions more often about what I actually wear, as in wearing right now.  So, this is a way for me to post it for everyone that might venture to this page, as well as a shameless amazon plug.  *If anyone happens to find better pricing than amazon, I'm all ears.

OK, so just to recap, if needed, the Morton's Neuroma that I HAD in my left foot is 100% healed and gone!  I can honestly say that all the MN woes I had for months are gone.  It's quite amazing what the sclerosing did and what a difference it makes to have my foot back again.  I've been working out at pretty high intensity with weight training, and I have been running on concrete with my VFFs.  Which, btw, anyone that is trying to get $ from Vibram FiveFingers, I hope you reconsider.  I've publicly opted to not accept any payment from them for the lawsuit.  The company makes a great product, but like anything else with your body and fitness, you have to ease into something new.

Anyway, back to the topic - here is a little widget (below and to the left) that shows the EXACT shoes I am currently working in, working out in, and wearing casually.  It's "winter" now in Arizona, so I'm wearing the Vivobarefoot boots a bit more, but technically all of these are casual.  I haven't had to wear anything super formal in quite some time, but from what I can tell, Vivo does have options with the shiny leather if someone needs to go that route.

For those in the U.S, have a very Happy Thanksgiving!  


Onward,
Shane

Feedback from you!

Hi everyone,
All is well on this end with the PAST Morton's Neuroma...but I wanted to check in with all of you, my readers from various countries, to see how things were going.  I get emails and Google Hangout blips from time to time, but I would love to hear a few things from YOU:

• Are you currently struggling with a painful MN?
• What have you investigated so far, in terms of correction?
• Are any of you using any of the shoes I have listed?
• Have any of you done the sclerosing, and if so, how is that going?
• How did you find this blog?
• Has this blog been of any help?
• Or any other info you want to share.

As I mentioned, my neuroma is completely gone.  I have been able to run and lift in my VFF (my favorite shoe for Arizona) frequently.  It is such a blessing to be able to say that and share that success.  Hopefully you are able to share in it as well.

God speed,

Shane

Working out! An update.

Well, as many of you might have figured out on your own, my updates are becoming less frequent due to the healing of the Morton's Neuroma I had!  So, with it being healed comes all of the things I was able to do before - working out, any outdoor activities with my friends or family, and simply enjoying the "normal" things.  So, I thank God that those troubling times of the MN are behind me.  But I am still hoping and praying that people find this blog, because I think this type of combination that I used allows the person to take a smarter approach to recovery without surgery, BUT this method also allows the person to come into a proper understanding of what he/she should be putting on their feet.

So, back to the update of working out: for a while now, I have been able to fully function for physical activity.  Lifting, running, etc.  I will admit, at first I had a bit of "I better ease into this" attitude, because I had been farting around with that MN for so long it had almost become a habit to be concerned with the "what if's" of if it gets strained or inflamed again.  But I am happy to say it hasn't.  I have been wearing my VFF, Altra, and Vivobarefoot shoes, and barefoot when I can, and things have gone beautifully.  And I will still wear my correct toes every now and then, but the frequency is decreasing now that the supportive tissues are strong and positioned properly.

Anyway, I hope this info can be shared by you to others that need it, because, again, the whole reason I started this was that I had a feeling, from all of the info I was reading online before, that people were not able to really overcome the MN they were suffering with, and it is beyond frustrating.  Especially when podiatrists might be trying to slam you right into orthotics and then putting you right into crappy shoes again.  Good podiatry means hearing your concerns, looking at the evidence and history of your feet, watching you walk, looking at the shoes you wear, and trying to work backwards for a real restoration of the foot, instead of just trying to mask the symptom or the pain, which would only be temporary.  You will know you are are at the right podiatrist office if they take the time with you and aren't trying to push you into buying something right away.

So, that's an update for anyone interested, as well as some info that might help you if you're working with a podiatrist.  

Bless you all,

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...