Hello Everyone,
This will be our final post on this site. We are pleased to announce that the book is now available on paperback and Kindle!
Please follow us on Facebook and Instagram at BeatingMN.
Here's to your foot health!
Shane
Sharing what I know on how to improve Morton's Neuroma as naturally as possible
Showing posts with label Nerve Pain. Show all posts
Showing posts with label Nerve Pain. Show all posts
Friday, September 7, 2018
Thursday, August 30, 2018
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
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
Saturday, August 18, 2018
I've written the Morton's Neuroma book!
Hey everyone,
Shane here. Just a heads up as this will be one of the final posts on this blog. A while back I decided to write a book which will basically serve as the platform, in addition to the Facebook page I created a while back. Facebook is an easier platform to update, share, and has better reach than this website when it comes to speed and control.
All that to say, there might be one more post on this blog, and then everything after that will be on our Facebook page, so please reference that, along with the book that I will be publishing in September 2018 (coming very soon)!
In the book, the details will be very clear on what I did, what options you should know about, and it's been condensed for easy reading. Anyone over the age of 10 will be able to read it - there are no crazy doctor-level words to make me sound smart - it's all in plain English, and can serve as a great guide if you or someone you know is wresting with Morton's Neuroma.
Be blessed,
Shane
Shane here. Just a heads up as this will be one of the final posts on this blog. A while back I decided to write a book which will basically serve as the platform, in addition to the Facebook page I created a while back. Facebook is an easier platform to update, share, and has better reach than this website when it comes to speed and control.
All that to say, there might be one more post on this blog, and then everything after that will be on our Facebook page, so please reference that, along with the book that I will be publishing in September 2018 (coming very soon)!
In the book, the details will be very clear on what I did, what options you should know about, and it's been condensed for easy reading. Anyone over the age of 10 will be able to read it - there are no crazy doctor-level words to make me sound smart - it's all in plain English, and can serve as a great guide if you or someone you know is wresting with Morton's Neuroma.
Be blessed,
Shane
Tuesday, February 20, 2018
Facebook page is now up!
Hi everyone,
Great news - I set a Facebook page up, which will help things stay a bit more current and restorer to post to. Over time, blogger had become a bit dated in terms of its platform and poor mobile interface from the owner side.
The link for the Facebook page is: https://facebook.com/beatingmn/
Catch us over there for some great updates, including my book, product reviews, and tips!
All the best,
Shane
Great news - I set a Facebook page up, which will help things stay a bit more current and restorer to post to. Over time, blogger had become a bit dated in terms of its platform and poor mobile interface from the owner side.
The link for the Facebook page is: https://facebook.com/beatingmn/
Catch us over there for some great updates, including my book, product reviews, and tips!
All the best,
Shane
Thursday, December 7, 2017
Update! Exciting things around the corner!
Hey friends,
So, I hope all is well with you across the globe. It's kind of crazy to know that this blog literally has global traffic from all "developed" countries. When I look at my analytics dashboard, it's just further proof to me that people are in serious need of help with Morton's Neuroma. Which brings me to what I believe is good news.
I'm going to be writing a book, and along with the book, create a Facebook page. The book will cover info from the blog, but it will flow better, and the Facebook page will function as somewhat of a supplement to the book, but will also have the other interactive elements that simply are not that great on a blog site.
So, chime in with any thoughts or comments. I'm planning on having the ebook done first, and it will be available on Kindle around the new year or shortly after, and once I have a publish date, the Facebook page will immediately follow.
Have a great night!
Shane
So, I hope all is well with you across the globe. It's kind of crazy to know that this blog literally has global traffic from all "developed" countries. When I look at my analytics dashboard, it's just further proof to me that people are in serious need of help with Morton's Neuroma. Which brings me to what I believe is good news.
I'm going to be writing a book, and along with the book, create a Facebook page. The book will cover info from the blog, but it will flow better, and the Facebook page will function as somewhat of a supplement to the book, but will also have the other interactive elements that simply are not that great on a blog site.
So, chime in with any thoughts or comments. I'm planning on having the ebook done first, and it will be available on Kindle around the new year or shortly after, and once I have a publish date, the Facebook page will immediately follow.
Have a great night!
Shane
Monday, January 19, 2015
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
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
Tuesday, December 23, 2014
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
Thursday, May 15, 2014
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...
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...
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