I wrote a document for Ledderhose Disease that may be helpful for some of you. If there is incorrect information or you feel something should be added or removed, please let me know.

There are two Facebook Groups I would suggest for you to join to see other's experiences and suggestions.

Ledderhose Disease or plantar fibromatosis support group https://www.facebook.com/groups/1652149925085536

Dupuytren's, Ledderhose and related conditions support https://www.facebook.com/groups/BritishDupuytrensSociety

Everyone's personal experiences are different so please figure out what the best option is for your personal treatment. I would strongly discourage surgery as an option because many people including myself had an effect of fibromas growing rapidly after surgery and many more developing that were way more painful than the original one.

Best of luck to all!