Dupuytrens Contracture and Ledderhose disease

I have searched the forum for treatments for these diseases. Has anyone used any of the protocols for these? I have this is one hand (Dupuytrens) and one foot (Ledderhose) - same condition. No treatment but surgery when it finally cripples your hands. It starts out with nodules on the tendons then, "cords" of thick tissue develop, pulling the fingers down (trigger finger for me). In the foot, you get nodules and /or thickening in the arch or ball of foot. No known cause, either, but it sounds from all I have read, like it could be an autoimmune condition.

suzie queue wrote: I have searched the forum for treatments for these diseases. Has anyone used any of the protocols for these? I have this is one hand (Dupuytrens) and one foot (Ledderhose) - same condition. No treatment but surgery when it finally cripples your hands. It starts out with nodules on the tendons then, "cords" of thick tissue develop, pulling the fingers down (trigger finger for me). In the foot, you get nodules and /or thickening in the arch or ball of foot. No known cause, either, but it sounds from all I have read, like it could be an autoimmune condition.

Suzie:

If not in the seach is because is a rare condition and nobody ask before. The most common is Arthritis that also is autoimmune disease. People apply a mixture of MMS activated with DMSO and put the joint with problems and also take MMS 1000 protocol. MMS will not make any harm to you so try it if work, Aleluya if Not please let us know so we can keep record of your success or not.
The outside application is 10 drops of MMS + 10 drops of HCL 5% react for 30 second then add 20 drops of DMSO mix and apply to the affected area.

Hello suzie queue

I also had Dupuytren and a cramped up foot, as part of my Rheumatoid Arthritis, so autoimmune. Prot. 1000 and just keep on going. Rubbing DMSO also helps and active excercise to stretch the contracted muscles.

Wishing you well.

marianne

I have dupuytren's also (at the nodule stage), and, in fact, have my initial trip for an orthopedist to see it (I'm self-diagnosed, but my PCP said I was right - my mother had it) is coming up July 10. - Mine has come up even with all the MMS I've done - although, I've not done 1000+, which may actually be better for it. Don't know if I have Ledderhosen -

Pam

I have a dear friend who is suffering from Ledderhose disease / plantar fibromatosis under her feeds.
It creates small noodles under her feeds that hurts a lot.
She haven't tried either MMS or DMSO yet, but I have presented her with the idea, though she is a little sceptical of it.
It would sure help if I could provide her with some testimonials or experiences with MMS / DMSO for this disease.
Do any of you have any luck with it so far?
What about foodbath, or maybe indeed rubbing MMS with DMSO on the feeds is a good idea!

I would try spraying / rubbing in full-strength CDS followed my DMSO on her feet and see if that helps. Let us know if it does or does not help. Thanks.