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I Have Ledderhose Disease

A Ledderhose Disease anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Ledderhose Disease. You're not alone. 42 People

    I Have Ledderhose & Dupuytren's Disease

    I am a 41 year old male who has Planter Fibroma on my feet and Dupuytren's on both hands. I am having surgery for my Ledderhose, despite all the horror stories I have read or heard regarding this method. The lump is the size of a large grape and I am nervous about the surgery. I...
    Metzie Metzie 41-45, M 2 Responses Jul 24, 2012

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    Hi I have ledderhose,

    I have thick tumors on the bottom of both feet and new small ones popping up, i had them taken out years ago but they came back, so bad my legs hurt, it is bad to have this diease but good to know I am not alone
    elviscentral elviscentral 51-55, F Dec 4, 2013

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    Suffering For Ten Years

    I have had ledderhose disease for over ten years now. I am at my wits end. I have gone to many doctors, acupuncturists, physical therapist. The only thing that seems to help is to have my feet on ice, or a good rub. I have not heard any promising reports on surgery. I have...
    CRUISERBUGS CRUISERBUGS 56-60 2 Responses Jul 22, 2011

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    My Story Without Surgery To Stop Or Reverse Progression...

    I noticed Ledderhose nodules around 3 years ago on both arches of my feet. They were pea sized and painful... After 2 years, they had progressed into marble sized and were very very painful. My left foot nodule is a little larger than the right. I showed my boss why I was...
    Garrett5302 Garrett5302 31-35, M 3 Responses Feb 24, 2013

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    Scared About Surgery For Ledderhose Disease

    Hello, this is my first post. In Oct. 2010 I had surgery on my left foot for what I was told was a fibroma on my planter fascitis tendon. Turns out they did not get it all and in less than 10 months it was back. This time 4 X as large. Now I am told it is Ledderhose disease. I...
    alaskandiane alaskandiane 56-60 3 Responses Jan 26, 2012

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    Ledderhose Disease In North Texas

    I've had numerous surgeries on my right foot and one on my left foot in 2005. The lumps reoccured in about 2 years but my surgeon retired and I've not found another surgeon willing to perform surgery. The three that I saw said I should just live with it. It is hard enough knowing...
    fiddlebows fiddlebows 56-60 5 Responses Jul 3, 2011

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    I Have Ledderhose Disease, Please Educate.

    Hi, I am a 26 yr old female, I am married with 1 child. I began to notice "lumps" in the arches of my feet when I was around 18 yrs old, I knew there was a high chance I would get them because my mom, uncle, great grandmother, and great great grandmother had them. I went on...
    footsymomma footsymomma 26-30, F 8 Responses Apr 28, 2010

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    A Bumpy Road

    The story starts about 3 years ago with the economic downturn. My family and I were forced to relocate and I returned to work. I have a good job but it requires being on my feet 8 to 12 hours a day. As the business grew so did the pain in my feet. First I was diagnosed with...
    bathnz83 bathnz83 46-50, F Aug 24, 2012

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    Ledderhose My Experience

    Growing up I was sure I had a little bump in the arch of my foot but there was no pain, no growth and nothing to be concerned about, then two years ago out of nowhere like the little menace that it is it started to grow and started to become really painful. I headed off to the...
    GaryKary GaryKary 22-25 2 Responses Feb 1, 2012

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    Lederhosen Story

    I am a 60 year old female with Lederhosen syndrome of both feet. I have been able to deal with the condition but lately, after wearing dress shoes with a heel I am experiencing severe cramping of my arches. Does anyone else have this? Is it related to Lederhosen or could I...
    Sorefeet1950 Sorefeet1950 56-60 14 Responses Feb 7, 2011

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    For Everyone Suffering From Ledderhose Disease

    I have been in unbearable pain for the past year... Getting painful cortisone shots in my left foot then going threw a minor surgery which hurt badly and left me unable to walk for 3 weeks, Only for it to return 3 months after the surgery, now the doctor wants me to go threw...
    naomi83 naomi83 26-30, F 3 Responses Nov 13, 2012

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    Please help anyone ..

    . I have just being diagnosed with Ledderhose's Disease this week :( I have a ultrasound scan to confirm its existence. This is all very new to me and I must say upsetting. The work I do entails me being on my feet all day. I am only seeing the Orthopaedic Surgeon next month...
    TheManicOz TheManicOz 46-50, M 3 Responses Dec 6, 2013

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    Facing Second Surgery

    Had surgery on both feet for this 9 years ago. Lumps are back. Mom and sister Both have had multiple operatios. Don't want to do it again. Anyone have success with any other method?
    Sharonricewallis Sharonricewallis 51-55 2 Responses May 31, 2011

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    Ledderhose Disease

    I have had ledderhose disease for about 4-5 years. I have been getting cortisone shots that seem to help for awhile but the lump always comes back. I am on my feet quite a bit as I babysit my 2 young grandchildren and run after them all day. I have read so many stories about...
    herouxm herouxm 66-70 5 Responses Mar 4, 2012

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    I have just been diagnosed with Ledderhose

    Disease my specialist is recommended surgery followed by radiation therapy however I have been warned there is no guarantees the lump will not return. I would like to know what others have trie very scarred of surgery when the internet advice is surgery is the last resort.
    sibsOz sibsOz 51-55, F 1 Response Jan 10, 2014

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    Related Experiences

    I am 49 and was originally diagnosed with keinbochs disease in my non-dominant hand about 15 years ago. I was diagnosed when I was in stage II. Too late to try any bone saving...
    kbjunkie kbjunkie 46-50, F 1 hr ago

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    I doubt I have Fibromyalgia, I have been suffering from migraine since childhood.. I always feel tired, fatigue and dizzy. The tiring feeling is always with me and it increased...
    dare86 dare86 26-30, M 1 day ago

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    It's been it's been about 8 years now that I've had lymes. It's been hell. What more is there to say?
    0210love 0210love 18-21, F 1 day ago

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    I fell in love... and just after got sores.... I got extremely high fevers and pain as well. but with this all being said I'm still waiting for my test results praying to God that...
    nomorepain898 nomorepain898 16-17, F 1 Response 2 days ago

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    It's really amazing that am cured of HERPES by a herbal medication. Oh is by this time last year I start feeling bad about my life, I feel pain everyday of my life but am very...
    TEGA32 TEGA32 26-30 3 Responses 2 days ago

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    Every power is alcoholic. Money property and prestige goals. Those are societys disease And how the wealthy led us wrong Going all the way back to wed forced.
    Converted Converted 46-50, M 3 days ago

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    The invisible pain. No one believes the level of pain this chronic disease causes.. I hate it so much.. being in pain on and off since 20 after acute pancreatitis I spent 7months...
    stefx85 stefx85 26-30, M 3 days ago

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    I am 23 years old and a week ago it was confirmed that I have ankylosing spondylitis.... My WHOLE life it's always been a possibility, my father has it and over his 50 years of...
    AlRoberts AlRoberts 22-25, F 3 days ago

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    I'm a 15 year old girl who has dermatillomania..I just really need someone who's close to my age to talk too who suffers with this disease like I do. My parents don't get it and I...
    sadiegracee sadiegracee 13-15 1 Response 4 days ago

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    RABIES DISEASES God bless Dr. Adagba for his marvelous work in my life, I was diagnosed of RABIES DISEASES since 2010 and I was taking my medications, I wasn't satisfied i needed...
    markrobbin111 markrobbin111 41-45, M 4 days ago

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    I have sufferers since May 2015 with pilonidal disease and it has been a really rocky road 😔 I would love to speak to anyone who has been going through the same/similar things...
    Kdnt Kdnt 18-21, F 4 days ago

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    My poor baby has autoimmune disease...my brother rescued him from being beaten by a bunch of kids and I've had him for about 2 years now and just love him to bits and now he's in...
    LilyAntoinette LilyAntoinette 18-21, F 4 days ago

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    How ironic, lupus is known as a woman's disease. 90% of all patients are women. 70 to 80% are black and ethic groups. And 20% are caucasion women. And 10% are male with the same...
    victoriasize6 victoriasize6 51-55, M 5 days ago

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    I considered posting this in an eating disorder category. But I really don't want to call it that. It feels like a bad word or disease. But I've struggled with this since I was...
    DeIuxedEdition DeIuxedEdition 18-21, F 1 Response 5 days ago

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    methacillian resistant staphylococcus aureus (mrsa) im not quite surr how i contracted it? either working in a hospital environment, or being a patient? this is a resistent strand...
    StreetgirlnamedDesire504 StreetgirlnamedDesire504 36-40 5 days ago

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    The doctors have diagnosed me with Spino Cerebellar Ataxia type 14. This means nothing. I don't trust the diagnosis. You see, I am 45 and have seen too many doctors for me to even...
    NMDewey NMDewey 41-45, M 1 Response a week ago

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    I was recently diagnosed with ET last February. My platelet counts were in the 700 range then. I currently live in Japan for work and have no other conditions besides high blood...
    Look4BeautyWithin Look4BeautyWithin 31-35, F a week ago

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    its important to get checked out and monitor. i not only had hyperthyroidism but it was caused from graves disease witch i inherited from my parents. i was severly hyperthyroidic...
    stormofself stormofself 18-21, M a week ago

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    Hello! I am doing a 10k run on October 4th 2015, for british heart foundation. I am doing this because i am a survivor of a heart disease, and would like to raise awareness and...
    amylouexoh amylouexoh 16-17, F Aug 23

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    Hello! I am doing a 10k run on October 4th 2015, for british heart foundation. I am doing this because i am a survivor of a heart disease, and would like to raise awareness and...
    amylouexoh amylouexoh 16-17, F 4 Responses Aug 23

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    Hello! I am doing a 10k run on October 4th 2015, for british heart foundation. I am doing this because i am a survivor of a heart disease, and would like to raise awareness and...
    amylouexoh amylouexoh 16-17, F Aug 23

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    I have just recently began the paleo diet in hopes to curb my pcos. so far on this journey, prior to the paleo diet change, I have lost 50 pounds from regular diet and exercise but...
    11Disasterpiece11 11Disasterpiece11 22-25, F Aug 22

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    So I contracted hepres about 2 yrs ago from an ex boyfriend who had it and didn't tell me. I actually found out from someone else he was seeing at the same time. I haven't...
    luethel luethel 22-25, F 1 Response Aug 22

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    PastBefore my incident I was a pretty active individual. My favorite hobby was bowling. I had even gone to Las Vegas to bowl in the Open Championship with my team mates. It was so...
    moeduff5141 moeduff5141 22-25, F Aug 22

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    I was diagnosed with DM in 2009 along with Celiac's disease, I guess I didn't realize what this disease was or how serious it was, at the time the Celiac's was my bigger concern...
    Jill2006 Jill2006 51-55, F Aug 21

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    Hi there my name is Nate And I'm a 25 year old male With cerebral palsy, On August 14 2015 I was diagnosed with Hashi modos I was shocked Because I have been a bodybuilder for the...
    natecr natecr 22-25, M Aug 21

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    Hi everyone! I'm a 23 year-old girl with a mild/moderate form of cerebral palsy. This is to say, I can walk unaided, my upper body part (neck, both hands) are completely OK and...
    Sunshine237 Sunshine237 22-25, F Aug 21

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