Pictures Of Scleroderma
Morphea Scleroderma
Scleroderma Esophagus

Morphia Scleroderma
Systemic Scleroderma Prognosis

Scleroderma Pictures Face
Skin Scleroderma

Scleroderma Crest Syndrome
Scleroderma Lung


Be the first to post a comment!

Post a Comment

Post a Comment:

Your Name:
Your Email
Your Comment
If you can read this, don't touch the following text fields.

Comments on

Bidhya Sagar Dhakal says:

It also will be in eye bows?

kingsley mary says:

What we plan with thoughts and actions for our future so we can enjoy retirement/older age, right? Life can change drastically when a rare, incurable disease such as Systemic Scleroderma attacks our bodies without warning! My life started changing in Fall 07 in my hands, progressing fast to include weak/painful muscles, swelling, loss of range of motion and depression until 3/30/09 diagnosed with Systemic Diffuse Scleroderma which no one has ever heard of until diagnosed and adding insult to injury, neither have most doctors, leaving patients to fend for themselves on how to find treatment for symptoms because Scleroderma cannot be treated as yet. Most Scleroderma patients look normal in appearance but the damage is extensive on the inside of our bodies, stage 4 kidney disease, hiatal hernia, pulmonary fibrosis, aneurysm in heart, GI issues, skin changes and Raynaud’s in hands & feet are just a few of my Scleroderma challenges. I am one of the more functionable patients and grateful I have doctors who care and support from Sweetheart, family and friends. Some patients don’t have either doctors nor support and rely on facebook Scleroderma chat groups for advice, love and support from people who relate and understand what they are experiencing. My life has changed dramatically from 5 1/2 yrs ago and I am grateful for my Scleroderma journey because the more I reach out to others the more rewarding my life has become. I am a patient advocate helping to educate and promote public and medical awareness of the desperate need to recognise Scleroderma as the life threatening disease it is. Scleroderma was first documented 260 yrs. ago, now we want awareness to help alleviate the horrible suffering this disease causes physically, mentally and emotionally. Please help.

Lisa Waters says:

I have Systemic Scleroderma diffuse. Have been soon Methotrexate for 2years now my Rhuematologist wants me to try Cyclophosphamide, as its obvious to her that Methotrexate is not working, just a little concerned with side effects of this drug and what would happen if I don't try it

Renee says:

Oh my,your stories I have read this morning sounds just like what I'm dealing with,all I wanted to do is look up on why my upper arms seem to be going num and weak more often than not,now I'm really scared!!!!! I have been seeing a rheumatologist with blood and uriue work done on me he deteriimant that I have scleroderma,raynauds phenomenon , new that for at least 20 plus years with raynauds, then I see on this site the look of people's hands as this progresses really really scares me. I'm 55 years old,don't want to become disable with this but it's not looking good for the home team. What's next and what is going on with this num feeling in my upper arms? I have a doc. Appointment on Monday so looking forward to that got a lot of questions? Just had a few questions.Have a good day. Got time on my hands since I'm off from work to do some studying on this this,still scared!!!

Vrushali says:

I'm really afraid of this,but i also don't want to miss my sister..i want to spend my whole life with her...

emeka says:

What are genetics associations of scleroderma?

saruqhossin says:

please give me right advice

saruqhossin says:

hello my name is mother name is hosnara bagum.she is 45+old.recently she fill some,,swell,few pain.then we are go to teratment on a medicen spicelist..then he watch and take some diagnostic.then he said inprove scleroderma,raynodus where do i go to which spicelist take i advice?

Sherry Hagerman says:

I have the conditions as you. Yes, this is a horrible disease . I also had a double lung transplant. My kidneys are ok but have esophagus is going to be wrapped due to acid reflux. I don't know how much more I can take. I believe I am now how Sjourns disease. It is secondary to scleroderma . Do you have any gastro problems? Are you on Prednisone , Vfend and cell pet. Nice to know there are others out there like me. God bless you!

deondra says:

My sister just die the other day from dat so sad 2 c her go
Privacy Policy

Images appearing on this site are available and thought to be in the public domain. We believe images are within our rights according to the
U.S. Copyright Fair Use Act (title 17, U.S. Code.)

Claims of Infringement
If you think that any photos appearing on this site infringe on your copyright, please let me know right away.
E-Mail :

Images and info on this site is not to be used for medical advice and no warranty whatsoever is made that any of the information, pictures , or captions are accurate.