Beginning of the Journey.

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.



Dundas Cactus Festival Parade Aug/2010

Dundas Cactus Festival Parade Aug/2010

Thanks all ...

Followers

Sunday, November 28, 2010

Afterwards



Dana’s dream to dance becoming reality one baby step at a time


Fatigue is decreasing and muscles are strengthening after Liberation treatment

DEBRA DOWNEY, SENIOR EDITOR


Published on Nov 24, 2010

Step by baby step, Dana Szwec’s dream to dance is inching toward reality.

Dana, who grew up in her mother Marilyn’s dance studio, has been confined to a wheelchair for the past five years. She suffers from primary progressive MS, and until earlier this year, there was little hope Dana would ever stand, let alone dance.

But after media reports circulated about the success of a medical procedure called the Liberation treatment, Dana decided she, too, would undergo the surgery.

Since it is not available in Canada, she underwent the 1 1/2-hour surgeryin Albany, N.Y., on Sept. 28.

“I feel great,” Dana said last week. “My mind’s much clearer and I’m much more awake. I feel like I have more energy, which is fantastic, and I don’t have that fatigue anymore.”

Before the treatment, Dana was finding it increasingly difficult to maintain the active schedule she sets for herself. Despite her challenges, Dana participates in Mac Wheelers, a twice-weekly exercise rehabilitation program for adults with a spinal cord injury, and yoga at the MS Society in Hamilton.

Just prior to the treatment this summer, Dana’s fatigue had become almost insurmountable. The 37-year-old would usually sleep nine hours a night, then be so tired by mid-afternoon she would nap for another couple of hours.

Eight weeks after the procedure, Dana’s lucky to get an afternoon siesta at all. Along with yoga and Mac Wheelers, she attends physiotherapy twice a week.

“In the morning when I wake up, I feel awake, I don’t feel I just want to sleep the day away,” she said. “I’m going five days a week. My fatigue is decreasing and my energy level is increasing.”

And Dana’s dream to dance once again seems possible. She can raise her leg a good six inches into the air, has some lateral movement and can stand with limited assistance.

“I’m very hopeful. I’m not walking yet or taking steps, but everything is baby steps. Everything takes time,” she said.

Dana and her mom say they have received “wonderful” support from the community that has helped pay the $10,000 U.S. cost of the Liberation treatment.

“We have had a tremendous amount of support, from Dundas, Stoney Creek, everywhere...” said Marilyn. “People have put money into the account (set up to help the Szwec family) that we don’t even know. It’s just been fantastic, and we want to thank everyone.”

As she inches toward recovery, Dana has also joined the chorus of MS sufferers urging the federal government to approve and fund the Liberation treatment in Canada.

“I’ve seen benefits from it. I don’t think it’s the placebo effect,” said Dana. “I know our government is very conservative and has to run trials and be absolutely certain, but thousands and thousands of people are leaving the country to have it done, and all I’ve heard are good stories.”

Developed by Italian neurologist Dr. Paolo Zamboni, the Liberation treatment involves a technique used to widen narrowed or obstructed blood vessels, a condition known as CCSVI or Chronic Cerebralspinal Venous Insufficiency.

In Dana’s case, doctors cleared her left jugular vein and two other areas of the azygos vein in her chest. Dana did not have stents inserted into her blood vessels, a process that is now reportedly causing problems for patients who underwent the treatment.

For the next year, Dana will travel to Barrie every three months for checkups.

With the Liberation treatment, her dreams once again seem attainable. Along with dancing, Dana hopes one day to stand at the top of the Dundas peak, 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,” she said. “I loved to get out and go hiking, up to the peak, for the fresh air, exercise and just being outside.”



Saturday, November 20, 2010

Biggest Changes



Biggest Changes: Energy, where did you come from? Hands and feet are warm, I can move my legs a little, Colour in my face is better and no puffiness. Yay!

This is the post I put on Facebook this week.  I forgot to mention my voice I'm told sounds better.  Today I wanted to stand with the walker, success!  Although only for a few seconds it is a start.  I'm out everyday exercising.  MacWheelers gym twice a week.  Physio twice a week and Yoga once a week.  I'm busier now than I have been in a long time, and I have no fatigue.  Truly amazing!