Oregon State athletic director Bob De Carolis deals with Parkinson's in his ...
It was June 10, a Friday, when Oregon State athletic director Bob De Carolis learned he had Parkinson’s Disease.He won’t ever forget the day he was diagnosed, or his immediate reaction: “Okay, so how much longer do I have to live?’’
De Carolis, 58, looked healthy and relaxed in his office at Gill Coliseum on Thursday as he talked about Parkinson’s, the potential impact it might have on his life, and his intention to stay on the job and perhaps be an inspiration or a help to other Parkinson’s patients.
De Carolis quickly learned that Parkinson’s isn’t a death sentence by any stretch of the imagination, that diet and exercise and the right mental attitude can work wonders.
He met other Parkinson’s patients attending a seminar at OHSU, each of them with inspiring stories, or helpful information about combating the illness that affects at least a million people in the U.S., probably many more.
De Carolis didn’t spend much time in the ‘why me?’ phase.
He didn’t sit in the doctor’s office feeling sorry for himself.
“There’s people out there with a lot worse things that what I’ve got,’’ he said.
“Is it going to be a challenge? Yeah. But people I don’t’ even know reached out to me and told me about cases of 15 years, 20 years, 25 years … I talked to a guy the other day whose mother had it when she was 42 and just died at 84.’’
Aside from some motor difficulty with his left thumb and left hand, and some occasional shaking of his leg, De Carolis has no visible symptons. He said he isn’t taking any medication, “but if I ever got stopped for DUI, I would be in trouble.’’
De Carolis said he appreciates all of the encouragement he is getting from the Oregon State community, from fans who might have sent him angry text messages in the past after a football loss.
“I’m in a lot of people’s prayer intentions,’’ said De Carolis. “I’m in pretty good shape from a prayer perspective.’’
While it was De Carolis’ wife, Sandra, who had suspicions “way back in February’’ that something serious was going on, De Carolis said his own suspicions went back to 2008 during the school’s tortured search for a new basketball coach.
What Do My Symptoms Mean - News
It is a roller coaster of emotions and not so nice physical symptoms. My decision will probably be made easier because we DO have some frozen embryos. If they don't take though, I don't know that I would go through the whole fresh IVF cycle again.
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What do all my symptoms mean? | Bruises Blog
Did he test you for Mono? Those symptoms are very similar to those in people with Mono, I know this because I had it when I was about your age. The only difference was my gland in my throat was swollen and I could barely talk or swallow. I think you need a second opinion sweetie, talk to your Mom about how you feel and see if you can get in to see another doctor. You need someone who will listen to you and help you start feeling better.
Hang in there!
coolbeanie27 Oh my, you poor thing, if things worsen and you get no good answers have your parents take you to the Mayo Clinic they will find out what it is- suggest to your MD for a referral if need be. Take care and Good Luck!
About four weeks ago, I came down with this illness. It started with a swollen, painful (right) underarm. Six days later, all my joints hurt. Since then, it’s gotten worse. It’s hard to walk, to type this question, to breath even! I’ve been to the doctor’s about ten times since I’ve gotten sick and Have been tested for nearly everything you could possibley think of. My other symptoms include: Fatigue, headaches, and this strange nausea that I get after I eat (if I don’t eat, I get really hungry. If I do eat, I get sick. Once the nausea goes away after about an hour, I feel really hungry again. I don’t over eat either). I have a couple of unexplained bruises too. I’m also thirteen, if that makes a difference. So what could I have? Has anyone ever had anything like it?
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