Morton's Neuroma is a condition that seems to affect runners a great deal considering the types of shoes we wear (studies show the number one cause of MN is the types of shoes we wear, or wore in my case).
I have developed a new bulletin board/forum website completely dedicated to Morton's Neuroma named Morton's Neuroma Talk!!!! MN Talk is a FREE discussion support group for those of us who are dealing with Morton's Neuroma where we can talk about this condition, how it is treated, and how it has effected our lives.
After some research I found that there truly isn't a dedicated bulletin board for MN out there. There are sites here and there that talk about health and medical conditions, etc., that may or may not talk about MN from time-to-time, hit or miss, but none dedicated solely to this condition.
I fully expect this brand new forum group to soon be jam packed with lots of information and advice from many experienced MN sufferers.
The address is http://www.mortonsneuromatalk.com. Please check it out, even if you don't have MN, just to see what we're all about. And definitely, if you know someone who has this condition, please share the web address with them. Thanks! -TJ
We will be getting a logo soon. (See how I said we? Hee.)
Thanks to Matt for his assistance in getting me started with this new project!
I have developed a new bulletin board/forum website completely dedicated to Morton's Neuroma named Morton's Neuroma Talk!!!! MN Talk is a FREE discussion support group for those of us who are dealing with Morton's Neuroma where we can talk about this condition, how it is treated, and how it has effected our lives.
After some research I found that there truly isn't a dedicated bulletin board for MN out there. There are sites here and there that talk about health and medical conditions, etc., that may or may not talk about MN from time-to-time, hit or miss, but none dedicated solely to this condition.
I fully expect this brand new forum group to soon be jam packed with lots of information and advice from many experienced MN sufferers.
The address is http://www.mortonsneuromatalk.com. Please check it out, even if you don't have MN, just to see what we're all about. And definitely, if you know someone who has this condition, please share the web address with them. Thanks! -TJ
We will be getting a logo soon. (See how I said we? Hee.)
Thanks to Matt for his assistance in getting me started with this new project!