I was very disappointed today when I looked at the plantar fibromatosis facebook page today and saw that due to the grouping update thingy that facebook has done the number of members is down to 2 and that includes me.
So if you have the disease and want to show your support on facebook then be sure to join the group here.
My experience with Ledderhose disease aka plantar fibromatosis. This information is not intended to replace your doctor. Information on this blog is provided for informational purposes only. You should not use the information on this web site for diagnosing or treating.
No comments:
Post a Comment