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
I think I saw only the ending some few years ago on HBO, but I remember being moved to tears. Literally. I hardly cry during movies, but this one was so touching that the floodgates opened. And I don't believe I saw the whole thing. So if you have a chance to see this movie, be sure to catch it. I, for one, would definitely make it a point to see the whole thing if I ever have the chance.
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.
8sc21
This film was made by Bob Saget about his sister's battle with scleroderma. To not only document what she and their family went through, but to put a face to the disease for us to better understand it. And on that it succeeds at every level.
It starts off slowly, introducing Hope's family, including her brother, a sitcom writer in California. Then we meet Hope, a single mother and teacher in her late thirties. Once the disease begins, she struggles to discover just what it is that's causing her pain, and only later learns what she's facing.
Her family's reactions of denial, confusion, anger, guilt, fatigue, and utter frustration are all displayed well and with feeling. Her brother's way of reacting to everything with a joke is annoying at first, and then you realize that this is his way of dealing with the crisis. The way he's always coped with life. It's given him a television career and a great home, and yet it can't help him in the face of his sister's illness. (Still, having said that, throughout the movie are jokes of poor taste, and the film would benefit if the first and last scenes, at the restaurant, were cut.)
But the star of the film is Delany, in a powerful performance. She goes to the core of the rage and grief over what has become of her body. It's a heart-rending journey as she tries to cling to her dignity, her family, and her life.
In short, this movie is not easy to watch, but necessary if you hope to understand what people with scleroderma are battling each day.
P.S. For an interesting side note, both Saget and Delany were involved in benefits for scleroderma even before Saget's sister became ill. And for more on Delany's involvement with the Scleroderma Foundation, see http://www.danadelany.com/extras-causes.htm
It starts off slowly, introducing Hope's family, including her brother, a sitcom writer in California. Then we meet Hope, a single mother and teacher in her late thirties. Once the disease begins, she struggles to discover just what it is that's causing her pain, and only later learns what she's facing.
Her family's reactions of denial, confusion, anger, guilt, fatigue, and utter frustration are all displayed well and with feeling. Her brother's way of reacting to everything with a joke is annoying at first, and then you realize that this is his way of dealing with the crisis. The way he's always coped with life. It's given him a television career and a great home, and yet it can't help him in the face of his sister's illness. (Still, having said that, throughout the movie are jokes of poor taste, and the film would benefit if the first and last scenes, at the restaurant, were cut.)
But the star of the film is Delany, in a powerful performance. She goes to the core of the rage and grief over what has become of her body. It's a heart-rending journey as she tries to cling to her dignity, her family, and her life.
In short, this movie is not easy to watch, but necessary if you hope to understand what people with scleroderma are battling each day.
P.S. For an interesting side note, both Saget and Delany were involved in benefits for scleroderma even before Saget's sister became ill. And for more on Delany's involvement with the Scleroderma Foundation, see http://www.danadelany.com/extras-causes.htm
This is an average movie based upon the real life events that took the life of Bob Saget's sister, who died as a result of the rare disease scleroderma. I found the movie interesting and informative. It is a tear jerker (especially if you have experienced the death of a family member as a result of a disease). I do not recommend this movie to those who want "entertainment" (as that it not it's purpose).
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