Si tengo tiempo, me gustaría investigar online si esta historia es real 100%

http://likes.com/g/9667693?page=5&v=13gU506j2j97AjLNB8H897u11zeZaz0fyw

Fue mal diagnosticada y paso hasta los 30 anios paralisada , cuando la enfermededad que realmente tiene se cura con una pastille.



Woman who spent 30 YEARS fighting debilitating cerebral palsy and undergoing operations discovers she has been misdiagnosed - and almost all of her symptoms can be cured by just one pill

• [size=32]Jean Sharon Abbott, 38, from Plymouth, Minnesota, was told she had spastic diplegia, a form of cerebral palsy, when she was four-years-old[/size]
  
• [size=32]She was 33-years-old when she learned she actually had dopa-responsive dystonia (DRD), a rare muscle disorder that can be treated with one pill [/size]
  
• [size=32]Jean, who was nearly immobile for 30 years, went on a 10-mile hike four months after she was given her new medication, which is known as L-Dopa[/size]
  
• [size=32]Despite her misdiagnosis, the mother-of-three insists she feels no resentment or anger about her doctor’s life-altering mistake [/size]
  

By Erica Tempesta For Dailymail.com
Published: 10:38 EST, 21 April 2015



A woman who spent 30 years of her life believing that she suffered from cerebral palsy, only to learn that she had in fact been misdiagnosed and almost all of her symptoms could be cured with just one pill, insists she feels no resentment or anger about her doctor’s life-changing error.
Jean Sharon Abbott, 38, from Plymouth, Minnesota, was told she had spastic diplegia, a form of cerebral palsy, when she was just four-years-old, she explained to The Mighty. But after three decades of suffering from muscle spasms, weakness, near immobility, as well as undergoing painful surgical procedures, she learned at the age of 33 that she actually had dopa-responsive dystonia (DRD), a rare, yet treatable, muscle disorder.
'Honestly, I’ve never had any negative thoughts about what I went through,' Jean told Daily Mail Online of her misdiagnosis, which saw her confined to a bed for much of her childhood. 

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Life-changing error: Jean Sharon Abbott can be seen recovering from surgery when she was 12-years-old. The 38-year-old has now discovered she was misdiagnosed with spastic diplegia, a form of cerebral palsy 

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Different life: Jean, who is pictured with her husband (L) and by herself (R), used a mobility scooter before she was diagnosed as having dopa-responsive dystonia (DRD), a rare, yet treatable, muscle disorder
While Jean admitted that there 'plenty of times' she wished she didn't have to deal with the physical symptoms associated with condition, including her dependence on others to complete everyday tasks, she noted that she still had a 'fantastic childhood' - thanks in large part to the unwavering support of her family and friends.
'Even though I had challenges, my parents were so good with dealing with my disability and didn’t “baby” me,' she explained. 'Also, I had true friendships that I never had to question. All of my life experiences made me who I am today - and I like me.'
 'I was expecting no results whatsoever and couldn’t imagine a life any other way
When Jean was first diagnosed with spastic diplegia, she was considered a textbook case, even though her MRIs and CAT scans didn’t show any typical symptoms of the disorder.
And because her neurologist was considered one of the best in the field, second opinions never yielded any other conclusions. 

'I had been seen by one of the best in the country, if not the world, and my parents even took me to the leading hospital in the US for a second opinion,' she recalled. 'They confirmed the spastic diplegia diagnosis and said that my doctor taught all of them.'
Jean said she never questioned her original diagnosis and instead chose to accept her physical struggles and focus on living her life to the best of her ability. 
'I was never one to dwell on my disability or to think about it too much, other than when I was at these doctor appointments,' she said. 'I guess I was too busy trying to live a normal life and having fun with my friends and family.'
By the time she was 12-years-old, Jean underwent a 'very painful' muscle transfer to prevent her knees from knocking together when she walked.

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Miracle drug: Jean, who was once nearly immobile, completed a 10-mile hike with her husband (pictured) four months after she started taking her DRD medication known as L-Dopa

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Happy family: Jean is pictured with her husband and their three children following her correct diagnosis of DRD
Although she compared the physical agony to open heart surgery, she said she was glad her parents encouraged her to have the procedure, which helped her a great deal and helped to prevent her from tripping over herself when she walked.  
Jean, who said she 'still can't get her knees to touch', noted that she was 'happy that it was a permanent procedure', although she would have done it again if needed.  
When she was in her late twenties, the mother-of-three had a pump implanted in her body to distribute medicine, but when she ended up over-medicated she visited a specialist who would eventually change her life forever.

 'I was never one to dwell on my disability or to think about it too much
Jean's new doctor questioned her original diagnosis and sent her to another neurologist.
Her new neurologist told her she had actually been living with DRD, noting that most of her symptoms would improve or disappear with a daily dose of a medication known as L-Dopa.
The neurologist explained that the symptoms of DRD, including the involuntary muscle contractions and tremors, are often mistaken for cerebral palsy or other disorders.
But Jean 'couldn't imagine having anything other than spastic diplegia' and confessed that she wasn't even going to fill the prescription until her husband persuaded to her to try it.
'When I began taking it, I was the biggest skeptic,' she said. 'I was expecting no results whatsoever and couldn’t imagine a life any other way.' 
Jean was given what she now knows to be her correct diagnosis on Good Friday in 2010 and just two days later, on Easter Sunday, she stood for the first time without assistance.


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New world: Jean can be seen using trekking poles during one of her hikes 

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True love: The happy couple posed for a photo when Jean still believed she had spastic diplegia

It soon became clear that the medication was working better than Jean could have ever imagined.
As she got stronger, her husband began working with her to increase her walking distance and fourth months later, they celebrated their 10th wedding anniversary by traveling the 1,200 mile road around Lake Superior - the location of their first honeymoon.
And not only was Jean able to walk to the touristy locations that she previously had to be carried to, she was actually able to complete a 10-mile hike along with her husband.
 All of my life experiences made me who I am today - and I like me
While Jean said that they took their time and had snacks along the way, she was amazed by her physical accomplishment.
'I was so proud of myself and thought that there are so many people in the world that physically can do stuff like this but choose not to,' she said. 'And I began to think of all the places I would love to travel with my family that wouldn’t have been an option before.'  


And while Jean realized that there are so many things she wants to try now that she can, she still insists that she doesn't have any regrets about receiving her diagnosis so late in life.
As someone who believes that everything happens for a reason, she noted that if she hadn’t been diagnosed with cerebral palsy, she probably would have chosen a different college, meaning she never would have met her husband and had three children with him.
'All I know is, I’ve never been one to live with regrets and I wasn’t about to start that thought process as the result of a new diagnosis,' Jean explained. 'Plus, I can do things that I never would have even considered before, so I have no reason to be angry or upset. I’m just so darn happy!' 

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Night out: Jean was wearing heels six months after she started taking L-Dopa to relieve her muscle spasms and tremors 

I began to think of all the places I would love to travel with my family that wouldn’t have been an option before 
Although L-Dopa has drastically changed her life, Jean still has to make sure that she gets plenty of sleep and remains as stress free as possible, or she can suffer from incredibly sore muscles and cramps, as well as issues with balance and tremors in her hands.
 I began to think of all the places I would love to travel with my family that wouldn’t have been an option before
'I work really hard to make sure I get the rest I need and not put too much pressure on myself. And I exercise every day,' she said. 'But it’s still way better than the alternative.'
She added: 'I’m so lucky to have this “miracle drug”. It has not only changed my life but the lives of my husband and kids.'
Five years after her proper diagnosis, Jean has become an advocate for raising awareness for DRD, which is often misdiagnosed.
And eight months ago, she decided to wean herself off of L-Dopa for a week so she could film herself walking, both on and off her medication, in order to help others recognize the symptoms of DRD.
Jean posted the video to YouTube in September 2014 and has since received emails from people who said her video helped them recognize DRD in either themselves or their loved ones.
She is also blogging about her journey on her website.  
'I feel that my story is so important because I’m sure there must be others out there who too are misdiagnosed with [cerebral palsy],' she said. 'If this story helps just one person I will be thrilled.' 


Read more: http://www.dailymail.co.uk/femail/article-3047729/Woman-spent-30-YEARS-fighting-debilitating-cerebral-palsy-discovers-misdiagnosed-symptoms-cured-just-one-pill.html#ixzz3fsFOcq2K

https://www.youtube.com/channel/UCsGCVjptcLkIPLp_PklisBA/videos