Does anyone have any info or been diagnosed with a accelerate type of ledderhose Disease??
I understand surgery should be the last resort, I really do!! I was schedualed to have a very large tumor sized nodule removed and the wait time for this was 6 months, I noticed a small small pin of a head nodule in the same area of the arch by the time I went for surgery it had grown larger then the original. The surgeon was shocked at the pace of these pesky things. He removed 2 large nodules a yr ago and now to date I have another three or four growing and this time they are in the arch as well now on the side of my foot. They are growing in a nice bed of scar tissue and hurt like hell as they grow. I'm also experiencing nerve pain and weird sensations ie: burning, bee sting style pain etc.
I wish I never had them out !! But doc says they were so large they were causing extensive damage to my gait and circulation is there anyone out there with this style of LD? I also have nodules in both hands
Damn Euro gene's!!