The life and death of a young woman who suffered from scleroderma, and how she and her family coped.The life and death of a young woman who suffered from scleroderma, and how she and her family coped.The life and death of a young woman who suffered from scleroderma, and how she and her family coped.
Babs Chula
- Doctor
- (as Babz Chula)
David Hurtubise
- Executive Producer
- (as Dave Hurtubise)
- Director
- Writer
- All cast & crew
- Production, box office & more at IMDbPro
Featured reviews
Just to clear something up, Bob Saget's point of this movie was not for it to be some fictional drama only to entertain it's viewers. His intention was to raise awareness of a very difficult and sad disease, called Scleroderma, that most people haven't even heard of but does effect more that several million people, that claimed the life of his sister. This movie is about her battle with that disease.
I was diagnosed with Scleroderma when I was 20 yrs old. It was a very difficult time in my life and everything changed. I have been living with this disease for 9 years, and it has claimed many of my organs. Now I can no longer have children. I hope people will watch this movie and have compassion for those who struggle with life-changing diseases and donate to it's research. Just maybe a cure could be found before long.
I was diagnosed with Scleroderma when I was 20 yrs old. It was a very difficult time in my life and everything changed. I have been living with this disease for 9 years, and it has claimed many of my organs. Now I can no longer have children. I hope people will watch this movie and have compassion for those who struggle with life-changing diseases and donate to it's research. Just maybe a cure could be found before long.
10NHUCKS
I really enjoyed the movie. My husband has scleroderma and was just diagnosed with it in January. While we were watching the movie we were comparing what was going on with him at this point to what was happening to hope. We can relate very well with this movie and the details of the disease was described perfectly. This movie was very touching and goes to show that this can happen to anyone because the cause of the disease is unknown, which is very hard to grasp. But knowing that there is no cure is even more hard to swallow, because now we are at the point of no return and death is the end result.
10NHUCKS
I wrote before about me and my husband watching the movie because my husband was diagnosed in January. Well, on the 19th of July he was finally called to rest by GOD. He had suffered for one short year from this disease but he suffered one year too long. I hope they find a cure from this disease even though it will not bring my husband nor my kids father back but it will at least save some other lives. To whom ever reads this, please do not take this subject lightly because this can to happen to you unexpectedly. My husband passed away at the sweet young age of 26. This disease is no joke.
This movie tells the story of a woman who is diagnosed with scleroderma---it is based on a true story.
Scleroderma is a rare disease that effects 300,000 people in the United States. There are many different forms of the disease and this story shows one of the most difficult types, systemic scleroderma.
"For Hope" tries to give an idea of how most people deal with scleroderma. Because it's rare, it's often misdiagnosed and a correct diagnosis can sometimes take a while.
It is 20 years since this movie was made. All of what is in the movie remains relevant. There still is no cure. There still is no answer on how people get it. But...there are some treatment options to delay the disease. Scleroderma is the most horrific autoimmune disease out there. This movie shows much of what the disease can do. It is well cast and well acted. It is well worth watching, but be prepared that you might shed some tears.
Scleroderma is a rare disease that effects 300,000 people in the United States. There are many different forms of the disease and this story shows one of the most difficult types, systemic scleroderma.
"For Hope" tries to give an idea of how most people deal with scleroderma. Because it's rare, it's often misdiagnosed and a correct diagnosis can sometimes take a while.
It is 20 years since this movie was made. All of what is in the movie remains relevant. There still is no cure. There still is no answer on how people get it. But...there are some treatment options to delay the disease. Scleroderma is the most horrific autoimmune disease out there. This movie shows much of what the disease can do. It is well cast and well acted. It is well worth watching, but be prepared that you might shed some tears.
I think the story lined talks about a disease and what it does not only to the patient but the family as well, and yes this is not a fun story line to watch, but a necessary one to tell the world so something might get done and cure can be found. If one person made a donation or one Dr realized how to help one of thier patients, then the story was worth telling.
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Written by Richard Rodgers (uncredited) and Lorenz Hart (uncredited)
Performed by Sheryl Crow
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