Agrega una trama en tu idiomaThe 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.
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- Guionista
- Elenco
Babs Chula
- Doctor
- (as Babz Chula)
David Hurtubise
- Executive Producer
- (as Dave Hurtubise)
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- Todo el elenco y el equipo
- Producción, taquilla y más en IMDbPro
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My name is Mendi and I was diagnosed with Reynaud's Phenomenon and Scleroderma (CREST) at the early age of 15. I saw the movie "For Hope" after I was diagnosed. I was told that I would live approximately 5 years. That is a great deal for a 15 year old to swallow. Not only was I having a hard time coping with the idea, I felt that I needed to hide my fear for my families sake because the news was overwhelming for them as well and I didn't want them to worry more. When I watched "For Hope", I cried for days and yet it also gave me hope. Since I was was 15, I have dreamed of meeting Sharron. When I heard she passed away, I had just lost my finger. Once again I cried because her death was a great loss to all current and future Scleroderma patients. God Bless Bob Saget for continuing to fight for all of us who suffer with Scleroderma and for what his sister believed in!
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.
The selfish son, the idiot brother, the rude parents...not an easy family to live or die in, but then few are. I've always hated Bob Saget but have to give him credit here for showing it like it really is, warts and all. Dana Delaney is one of my all-time favorite actresses--if you've never seen "China Beach" do yourself a big favor--and the only reason I watched this. I'm glad I did...sad, but glad. What a terrible disease.
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
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.
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By what name was For Hope (1996) officially released in Canada in English?
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