My Single Mom Life

Last night Mindy and I went and saw Extraordinary Measures at the Muvico in Tampa.
Many thanks to CBS films for letting us be at the advanced screening of the film for free, it was most definitely appreciated as we both needed a night out, just us girls, so we could see a good movie, talk, and have some fun.

Synopsis

"Extraordinary Measures" is inspired by the true story of John Crowley, a man who defied conventional wisdom and great odds, and risked his family's future to pursue a cure for his children's life threatening disease. From his working class roots, John Crowley (Brendan Fraser) has finally begun to taste success in corporate America. Supported by his beautiful wife Aileen (Keri Russell) and their three children, John is on the fast track. But just as his career is taking off, Crowley walks away from it all when his two youngest children, Megan and Patrick, are diagnosed with a fatal disease. With Aileen by his side, harnessing all of his skill and determination, Crowley teams up with a brilliant, but unappreciated and unconventional scientist, Dr. Robert Stonehill. (Harrison Ford) Together they form a bio-tech company focused on developing a life-saving drug. One driven to prove himself and his theories, the other by a chance to save his children, this unlikely alliance eventually develops into mutual respect as they battle the medical and business establishments in a fight against the system - and time.

I thought the movie was going to be a total tear-jerker, but it wasn't.
There was only one scene where I felt like crying like the main character did, John Crowley, played by Brendan Frasier, when he thought he had screwed up so bad that he ruined his chance to help save his kid's lives.
Based on a true story, John Crowley was doing everything that he could do and think of to try and save the lives of his kids who suffer from Pompe Disease.
In Pompe Disease, normally, the body uses GAA to break down glycogen, a stored form of sugar used for energy. But in Pompe disease, mutations in the GAA gene reduce or completely eliminate this essential enzyme. Excessive amounts of glycogen accumulate everywhere in the body, but the cells of the heart and skeletal muscles are the most seriously affected.
Kids with the disease often don't live much past the age of 9-10, so John Crowley gave up his job, moved his family across the country, to try and prove the theories of Dr. Robert Stonehill, played by Harrison Ford.
Thanks to the hard work and sacrifice of both Crowley and Stonehill, an enzyme replacement therapy drug was created and it is actually working to help babies and kids with the disease to keep their hearts and other organs from growing too large and breaking down the muscles.

It was a really fantastic movie, I really enjoyed it, and as I said, it wasn't the tear-jerker that I thought it was going to be, not at all.
It was a movie about the hard work, determination, and love a parent has for their children.
I would highly recommend the movie to anyone to go see, it was definitely a movie worth watching as both Frasier and Ford did an outstanding job in their roles.
Harrison Ford plays a really eccentric and cranky scientist with a theory about the disease and how to treat it, but he's never had a drug go to trials, and never had a drug approved, so getting the venture capital needed to make and test the drug was an impossible feat for him.
That's where Frasier's character comes in, he has the business skills needed to get people to invest, he does whatever he has to to get the funding so Stonehill can get the drug made and into trials, and then approved, including having to sell-out to a larger drug company so that everything can happen at a much faster pace.
The things he did, he had to do even though it really angered Stonehill to have to sell-out and go work in a huge pharmaceutical company, but it had to be done, Crowley's kids were drying, they didn't have much time left at all.
In the end, Crowley even had to be fired from his job in order to get his 2 kids into the sibling test trials for the enzyme replacement therapy.

As a parent, I would do anything for my kids, I know how Crowley felt, do anything, everything, to try and save his kids.
Luckily, my sons don't have any life-threatening diseases like this, but Mark does have problems with his spine and I am fighting with the doctors and insurance almost every single day to get him treated now, not in 15-20 years when it may be too late to help him, when it may be so late that he ends up like me.
He's 18, has his whole life ahead of him, I can't let him end up like me, so like Crowley, I will fight and do what it takes to help my son get the medical treatment he needs now, not later.

The movie isn't that long, so we made it home before midnight, and I was dead tired from the long ride there and back, and sitting in the theater seat all that time.
I woke up this morning exhausted, I had big dark circles under my eyes, so I grabbed my eye ice pack and laid back down on the couch for another couple of hours.
I'm still tired but have a lot to do including the grocery shopping.
Ugh.

Oh, when we got to the theater, CBS had saved us our seats because I had asked to be in the handicapped row, middle seating if possible because of the tilt of my head, I cannot be way down front.
Sharon, the host of the screening, escorted us to our seats which she had roped off with caution tape.
The theater was totally packed, there were a lot of people there for the screening, so walking into a packed theater and being escorted to our roped off seats was kind of embarrassing.
Everybody was staring at us because she escorted us to the roped off section and she said really loud that the seats were for the VIP movie screeners for CBS Films, and that they had to hold up the movie for a few more minutes for a few more VIPs.
Ha!
All of the other screeners were from some group that I want to look up, GOFOBO or something like that, but we were treated as VIPs, given special seating, and thanked like a million times, so it was fun and kind of embarrassing, but kind of cool too to be given special treatment.
So thank you very much to CBS Films for allowing us to be a part of the advanced screening.

Extraordinary Measures will be in nationwide release on January 22nd, and I highly recommend the movie.