Dana has Primary Progressive Multiple Sclerosis. This rare form of MS has been successfully treated with a surgical procedure similar to ballon angioplasy used for heart patients. This procedure was pioneered by Dr. Paolo Zamboni in Italy. Currently, this procedure is not available in Ontario. The hope of leading an active life once again is taking Dana on a journey to Albany, New York, to undergo treatment ....
Beginning of the Journey.
Dana and Marilyn
Dana Szwec to undergo surgery in U. S. to help relieve symptoms of MS.
By Debra Downey, Senior Editor, Dundas Star News.
Jul 29, 2010.
Dana Szwec has a dream. It’s not a big dream, like winning the lottery or travelling the world.
Dana’s one wish is simple. She wants to stand up again, preferably at the top of Dundas peak with the wind whispering through towering maple trees, a butterfly’s gentle wings brushing her ankles and her lungs filling with cool, refreshing air.
“If I could walk again, that’s what I’d do. I really miss the trails around Dundas. I loved to get out and go hiking, up to the peak, for the fresh air, exercise and just being outside".
Dana, 37, hasn’t been able to stand for five years. She doesn’t have any balance and she can’t move her legs. Her once healthy and active body has been ravaged by multiple sclerosis. The unpredictable, often disabling disease attacks the central nervous system. There is no cure.
Dana was just 29 when she began experiencing symptoms. A dancer since the age of 2 1/2, Dana is a graduate of the Ryerson University dance program and had, for eight years, been affectionately known as “Miss Dana” by her young students at her mother’s dance studio.
Dana had planned to take over Szwec School of Dance from mom Marilyn. She was learning the ropes, had applied for and received an arts council grant to attend a small business and arts course at Mohawk College.
Dana had more or less grown up at the Szwec school. She taught younger children jazz, tap and ballet, performed in shows at nursing homes and community events and showed off her own immense talent during solo performances at annual recitals.
By the time Dana had reached her early teens, there was no question she would pursue a career in dance, one day take over from mom.
Marilyn vividly remembers the day MS crept into their lives, heartlessly and forever changing their plans.
“Dana was at the front of the studio, sitting at the desk there, trying to read a paper about six inches from her face. I knew something was wrong, and that seemed to trigger everything,” said Marilyn.
As is typical for multiple sclerosis, the first symptoms were vision problems. Dana’s eyesight had started to jump and she experienced extreme fatigue.
Marilyn sold the dance studio in 2004. She had operated it for 32 years.
•••
Dana didn’t believe the diagnosis of multiple sclerosis when she finally heard it from the head neurologist at St. Michael's Hospital in Toronto.
She knew a little about the disease, had participated the MS Society’s fundraising read-a-thons as a child.
“I was in complete denial,” Dana said of her feelings at the time. “There was no way. It’s got to be something else.”
But reality eventually set in. Dana was presented with two options to halt or delay the disease — stem cell replacement or chemotherapy.
Dana opted for chemotherapy. She suffered through the treatments, lost her thick dark locks. It did, however, keep her well for two years. Dana used a walker but managed to get around.
Five years ago, things went downhill...fast.
Dana has Primary Progressive MS, which is characterized by a slow accumulation of disability. Only 10 to 15 per cent of people diagnosed with MS have primary progressive. There are no medications and nothing, until very recently, to treat it.
Despite her physical challenges, Dana has tried to stay active through Mac Wheelers, a twice-weekly exercise rehabilitation program for adults with a spinal cord injury, and yoga at the MS Society in Hamilton.
“Although it’s getting harder and harder to move my body, I am still keeping up with my programs,” she said.
For the past five years, Dana’s friends, family and supporters have participated as a team in the annual MS Walk For the Cure. Dana’s Dancin’ Divas and Dudes has won awards for best team name, best team spirit and best costume.
Dana picks a different theme each year; this spring, they were the Pirates. The 40 or so team members have raised more than $10,000 in the past five years.
Dana looks forward to the annual fundraising event.
“My life has definitely changed within the last eight years. It is definitely not what I thought it would turn out to be,” she said. “However, people keep telling me how great my attitude is. I do choose to be positive, besides I can’t change what has happened to me. It’s not what I expected, but I do still have to live, and it’s not in me to just shut down.”
•••
Last November, Dana and her mom tuned in to W5, a Canadian current affairs program that highlighted the work of Dr. Paolo Zamboni. The Italian neurologist has treated MS patients through angioplasty to widen veins in their necks, a condition known as CCSVI or Chronic Cerebralspinal Venous Insufficiency. The surgery is fairly simple; people around the world have experienced positive results. For some, the improvement is immediate; others get a little better each day.
News of Dr. Zamboni’s success has spread around the globe. Dana believes it can help her.
Since the surgery is not not yet available in Canada, Dana must travel to Albany, N. Y. Her surgery is scheduled for Sept. 28. It will cost about $10,000 U. S. for the aptly named Liberation Treatment.
One of Dana’s friends has circulated a letter to service clubs asking for donations. Dana and Marilyn both hope the community will also find it in their hearts to contribute.
“Nobody knows what’s going to happen,” said Dana. “I'm hoping with the Liberation Treatment, I will become independent, productive, and with a renewed quality of life, be able to give back to my community.”
An account has been set up at the Royal Bank on King Street West in Dundas to help the Szwec family, account number 5024120, transit number 01262.
By Debra Downey, Senior Editor, Dundas Star News.
Jul 29, 2010.
Dana Szwec has a dream. It’s not a big dream, like winning the lottery or travelling the world.
Dana’s one wish is simple. She wants to stand up again, preferably at the top of Dundas peak with the wind whispering through towering maple trees, a butterfly’s gentle wings brushing her ankles and her lungs filling with cool, refreshing air.
“If I could walk again, that’s what I’d do. I really miss the trails around Dundas. I loved to get out and go hiking, up to the peak, for the fresh air, exercise and just being outside".
Dana, 37, hasn’t been able to stand for five years. She doesn’t have any balance and she can’t move her legs. Her once healthy and active body has been ravaged by multiple sclerosis. The unpredictable, often disabling disease attacks the central nervous system. There is no cure.
Dana was just 29 when she began experiencing symptoms. A dancer since the age of 2 1/2, Dana is a graduate of the Ryerson University dance program and had, for eight years, been affectionately known as “Miss Dana” by her young students at her mother’s dance studio.
Dana had planned to take over Szwec School of Dance from mom Marilyn. She was learning the ropes, had applied for and received an arts council grant to attend a small business and arts course at Mohawk College.
Dana had more or less grown up at the Szwec school. She taught younger children jazz, tap and ballet, performed in shows at nursing homes and community events and showed off her own immense talent during solo performances at annual recitals.
By the time Dana had reached her early teens, there was no question she would pursue a career in dance, one day take over from mom.
Marilyn vividly remembers the day MS crept into their lives, heartlessly and forever changing their plans.
“Dana was at the front of the studio, sitting at the desk there, trying to read a paper about six inches from her face. I knew something was wrong, and that seemed to trigger everything,” said Marilyn.
As is typical for multiple sclerosis, the first symptoms were vision problems. Dana’s eyesight had started to jump and she experienced extreme fatigue.
Marilyn sold the dance studio in 2004. She had operated it for 32 years.
•••
Dana didn’t believe the diagnosis of multiple sclerosis when she finally heard it from the head neurologist at St. Michael's Hospital in Toronto.
She knew a little about the disease, had participated the MS Society’s fundraising read-a-thons as a child.
“I was in complete denial,” Dana said of her feelings at the time. “There was no way. It’s got to be something else.”
But reality eventually set in. Dana was presented with two options to halt or delay the disease — stem cell replacement or chemotherapy.
Dana opted for chemotherapy. She suffered through the treatments, lost her thick dark locks. It did, however, keep her well for two years. Dana used a walker but managed to get around.
Five years ago, things went downhill...fast.
Dana has Primary Progressive MS, which is characterized by a slow accumulation of disability. Only 10 to 15 per cent of people diagnosed with MS have primary progressive. There are no medications and nothing, until very recently, to treat it.
Despite her physical challenges, Dana has tried to stay active through Mac Wheelers, a twice-weekly exercise rehabilitation program for adults with a spinal cord injury, and yoga at the MS Society in Hamilton.
“Although it’s getting harder and harder to move my body, I am still keeping up with my programs,” she said.
For the past five years, Dana’s friends, family and supporters have participated as a team in the annual MS Walk For the Cure. Dana’s Dancin’ Divas and Dudes has won awards for best team name, best team spirit and best costume.
Dana picks a different theme each year; this spring, they were the Pirates. The 40 or so team members have raised more than $10,000 in the past five years.
Dana looks forward to the annual fundraising event.
“My life has definitely changed within the last eight years. It is definitely not what I thought it would turn out to be,” she said. “However, people keep telling me how great my attitude is. I do choose to be positive, besides I can’t change what has happened to me. It’s not what I expected, but I do still have to live, and it’s not in me to just shut down.”
•••
Last November, Dana and her mom tuned in to W5, a Canadian current affairs program that highlighted the work of Dr. Paolo Zamboni. The Italian neurologist has treated MS patients through angioplasty to widen veins in their necks, a condition known as CCSVI or Chronic Cerebralspinal Venous Insufficiency. The surgery is fairly simple; people around the world have experienced positive results. For some, the improvement is immediate; others get a little better each day.
News of Dr. Zamboni’s success has spread around the globe. Dana believes it can help her.
Since the surgery is not not yet available in Canada, Dana must travel to Albany, N. Y. Her surgery is scheduled for Sept. 28. It will cost about $10,000 U. S. for the aptly named Liberation Treatment.
One of Dana’s friends has circulated a letter to service clubs asking for donations. Dana and Marilyn both hope the community will also find it in their hearts to contribute.
“Nobody knows what’s going to happen,” said Dana. “I'm hoping with the Liberation Treatment, I will become independent, productive, and with a renewed quality of life, be able to give back to my community.”
An account has been set up at the Royal Bank on King Street West in Dundas to help the Szwec family, account number 5024120, transit number 01262.
Dundas Cactus Festival Parade Aug/2010
Thanks all ...
Followers
Thursday, October 14, 2010
Fall Weather
Hello all,
It has been just over two weeks and I feel really good, since having my surgery. Little minor changes are starting to occur. Most of them are not visible however the biggest change so far is that I'm able to move my lower legs. It was quite exciting when I discovered this.
Other changes include a much better energy level and clearer thought process. The fall weather is making me little tired, especially on the damp rainy days. I think everybody feels that way though.
I've been very busy. I go to Mac Wheelers gym Monday and Thursdays, I've started physiotherapy every Tuesday and Fridays and on Wednesday I go to the MS Society for the yoga program. Weekends are basically my free time. LOL
I will keep you all posted as the bigger changes occur.
Tuesday, September 28, 2010
On the mend
I've been out of the medical center for about five hours. Still feeling the effects of the sedative. Spent the afternoon napping. No major changes yet. Will have to start looking at the little things. Still very tired. We'll go back to the medical center tomorrow. The procedure was a little painful, especially my left jugular vein. The staff was very good and encouraged me to breathe through the pain. It only lasted about a minute. Lots of rest and baby steps to full liberation. :)
Sunday, September 26, 2010
Tuesday, September 21, 2010
Monday, September 20, 2010
Sunday, September 19, 2010
Less than a week
It's hard to believe that we will be in Albany one week today. The time is flying, I think I've mentioned that before LOL
The dance last night was fabulous. I saw many many friends and some family to. A lot of people I have not connected with in years. Many childhood friends, many students I used to teach, my dancin' divas, some family and many supporters and friends. The room was filled with much love. I am so grateful to have so many people that care about me in my life. Thank you to all of you. Your positive thoughts and prayers are what I'm taking with me on this journey. And that means more to me than you'll ever know!
The dance last night was fabulous. I saw many many friends and some family to. A lot of people I have not connected with in years. Many childhood friends, many students I used to teach, my dancin' divas, some family and many supporters and friends. The room was filled with much love. I am so grateful to have so many people that care about me in my life. Thank you to all of you. Your positive thoughts and prayers are what I'm taking with me on this journey. And that means more to me than you'll ever know!
CACTUS PARADE VOLUNTEERS:
(from bottom left)
Dianne, Cheri, Sheila, Suzanne, Debbie, Darlene, Benjamin, Bruce
(with Dana in the car and Marilyn taking the photo)
Friday, September 17, 2010
This is a test run only -- but is a pleasant interlude.
Thursday, September 9, 2010
It will be here before I know it!
2 1/2 weeks to go! I truly believe that this procedure is timely for me. This disease is progressing. I can feel it and other people can see it. Can't wait for the changes to come.
Fatigue is still an issue. Numbness in my hands and feet is still there. Absolutely no mobility in my lower body. My eyesight however seems to be better. I'm not having as many choking spells, so a few positive things happening. People always say I'm positive, I guess it's true.
I can't believe it's been five years of using a wheelchair. This country is very good at supplying medical aids and assistive devices. I have had two motorized wheelchairs in the last five years. They have been fully funded. I have no complaints at all.
However, I find it very hard to believe that this country is taking so much time to approve this treatment. It's pretty sad when people have to mortgage their houses and use their life savings to go to foreign countries such as Poland, Kuwait, India and Costa Rica just to name a few, for the liberation treatment.
It shows me just how lucky I am. I am thrilled to be going to the states, instead of somewhere overseas. I have many supporters who have helped me to fund this procedure. Just a couple of examples of how fortunate and blessed I am. It's an answer to prayer. And I am truly grateful!
Fatigue is still an issue. Numbness in my hands and feet is still there. Absolutely no mobility in my lower body. My eyesight however seems to be better. I'm not having as many choking spells, so a few positive things happening. People always say I'm positive, I guess it's true.
I can't believe it's been five years of using a wheelchair. This country is very good at supplying medical aids and assistive devices. I have had two motorized wheelchairs in the last five years. They have been fully funded. I have no complaints at all.
However, I find it very hard to believe that this country is taking so much time to approve this treatment. It's pretty sad when people have to mortgage their houses and use their life savings to go to foreign countries such as Poland, Kuwait, India and Costa Rica just to name a few, for the liberation treatment.
It shows me just how lucky I am. I am thrilled to be going to the states, instead of somewhere overseas. I have many supporters who have helped me to fund this procedure. Just a couple of examples of how fortunate and blessed I am. It's an answer to prayer. And I am truly grateful!
Friday, September 3, 2010
Less than a month
I can't believe how fast time is flying. A month from now I hope to be in full recovery mode and on the upswing. These last few weeks have been challenging. My fatigue level has been increasingly high. All I want to do is sleep. I do however keep going. My regular routine of going to the gym twice a week and yoga once a week has been kept up. I'm hoping for much more energy and improved mobility after the procedure.
I thought I'd better start typing on my blog to let you all know I am here. Hoping to get on here a little more often or regularly as time keeps flying.
My friend Mary had the procedure done last week and is doing very very well. This is very encouraging to me. She is my inspiration. I only hope to be doing as well as her after my surgery. Way to go Mary!
I will type more later.
I thought I'd better start typing on my blog to let you all know I am here. Hoping to get on here a little more often or regularly as time keeps flying.
My friend Mary had the procedure done last week and is doing very very well. This is very encouraging to me. She is my inspiration. I only hope to be doing as well as her after my surgery. Way to go Mary!
I will type more later.
Wednesday, September 1, 2010
Dana is about to write a blurb on her blog. Now that her computer is working okay she can, when her energy levels allow it, type up a storm. :-)
Saturday, August 28, 2010
Counting down
One month today and my procedure will be starting. I'm hoping and praying for some symptom relief and improved mobility.
The real beginning ...
Today, one month today is the real beginning. Dana will be in Albany on September 28th, 2010 filled with hope and full of all the wishes we continually extend to her.
We wish you well, Dana, we all wish you well ...
Today, also, she wanted very much to write but she is having a little bit of trouble with her computer, plus her hands will not do what she wants them to do! Her computer problems we will fix, her hands Albany will fix.
We wish you well, Dana, we all wish you well ...
Today, also, she wanted very much to write but she is having a little bit of trouble with her computer, plus her hands will not do what she wants them to do! Her computer problems we will fix, her hands Albany will fix.
Saturday, August 21, 2010
Dundas Cactus Festival Aug/2010
Thursday, August 19, 2010
Cactus Festival Parade
The Festival Parade starts tonight (Aug 19th) at 6.45pm and Dana is in it. Her team members will be distributing explanatory flyers to the spectators.
Fingers crossed for good weather.
Fingers crossed for good weather.
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