EPILEPSY AWARENESS 2009

EPILEPSY AWARENESS 2009 Providing Quality Information & Support on Epilepsy for Individuals, Families, & The Community

What brought me to advocating, public speaking & writing awareness information to families managing epilepsy? Over the years I have gathered information about epilepsy & its many related issues through personal experience, research & from working directly with the professionals in Neurology.
- I witnessed my first seizure at age 4
- lost a family member who had epilepsy to su***de when I was 12 y

ears old
- my brother developed epilepsy at age 13/14
- my own personal battle with uncontrolled tonic clonic epilepsy began when I was 29 years old (1995). Volunteer: Epilepsy Huron-Perth from 1996 – 2009
In the spring of 1996 I was introduced to & became involved with Epilepsy Huron-Perth. Within a couple of years I was asked to join the Board of Directors & in 1998 (when my uncontrolled seizures caused me to leave the workforce) my direction became fully involved in volunteering & working on the Board. I became President for the Epilepsy Organization in 2004, continuously volunteering, up until my decision to retire in the summer of 2009. Retirement in 2009 was partly due to a move which led me to creating my first internet support page, Epilepsy Awareness 2009. I have continued to share information & support individuals through the internet. I also write & continue to speak publicly about Epilepsy whenever the opportunity arises. Other Achievements:
1986: Government Hairstylist Licence
1999: Diploma - Interior Design (Highest Honors)
2007: Government Certificate - Recognition for Continued Commitment to Volunteerism

05/07/2026
When I was diagnosed with a rare form of epilepsy 30 years ago my husband & I had 3 young kids. At the time our kids wer...
05/07/2026

When I was diagnosed with a rare form of epilepsy 30 years ago my husband & I had 3 young kids. At the time our kids were excelling at an average rate & had no stand out health concerns. However, because Epilepsy is in my family the doctors were concerned there was a chance I could pass my condition onto my children.
So seeing a chance to learn from our family, a team of doctors in the neurological unit offered us an opportunity for all of our children to have free testing; MRI’s, EEG’s, Bloodwork.
After a short discussion, we turned their offer down. We felt not knowing was best because our focus needed to remain on what was actually facing us; not on fearing challenges that haven’t happened & may never happen. Steve & I knew if one or more of our kids had a genetically higher risk of getting epilepsy then we would only worry more for our kids & their future.
As it was, every time our kids witnessed my seizures it meant re-assuring them again; everything’s ok, mom will be fine. So putting them through a pile of tests did not make sense to us as a way to lessen our kids burden. We wanted to let our kids just live & be kids, as often as possible.
Now it’s many years later & I’m really glad at our choices for our family. So far all 8 of them are healthy; our children, our grandchildren, & now a great grandson too. So fingers crossed🤞🤞
We’ll continue to pray & hope they never ever experience what myself & many others go through with epilepsy. 💜

03/25/2026

Tomorrow
March 26th
Let’s Rock
Purple Day!

Very Interesting!…
02/24/2026

Very Interesting!…

This talk was given at a local TEDxSnoIsleLibraries event and produced independently of the TED Conferences. Frances Lewis, university professor and research...

Over the years I have shared a variety of information in hopes to increase awareness about the complexity of brain relat...
01/28/2026

Over the years I have shared a variety of information in hopes to increase awareness about the complexity of brain related disorders.
I realize not everything posted here is going to be something of value to everyone. But I can’t tell you how much I truly hope I am helping by sharing the information I feel is valuable.
My experiences began early on when I witnessed my step dad having a grand mal seizure (now called tonic clonic seizures). I was only 4 years old. Little did I know then, by 29 years of age I would also start having tonic clonic seizures.
Ironically I started advocating for epilepsy in public school, winning the public speaking competition for my school in grade eight. When I won, I went on to compete in the London city competition. Unfortunately though, my epilepsy speech didn’t place in the top three. But it was the 1970’s so I’m not really surprised. I was also chosen valedictorian that year. When I think about that now, it’s probably good we don’t always know the future. My valedictorian speech would’ve been slightly different then for sure lol
On the positive side, my knowledge base regarding neuroscience & seizure disorders has grown a lot. When I developed my own uncontrolled seizure disorder I joined the local epilepsy support community & continued to learn, finding myself drawn to all the many stories & intrigued to understand the different variables from one situation to others that are related. Because my own diagnosis is complicated & I have family members who manage seizures, as well as have lost family & friends who had seizure disorders I am driven to research everything medically related. My husband says I should be a doctor. But at my age & the cost for education that’s a pipe dream lol.
However I do have some accomplishments. I have wrote & shared newspaper articles about epilepsy, spoke to groups at factories, banks, nursing homes, schools, golf tournaments & various charity events. As well as being interviewed on radio & tv.
When I created Epilepsy Awareness 2009 I had a personal level understanding of chronic disorder challenges & understood the physical, emotional, & financial complications that often arise. Average day to day challenges are compounded, making life extra challenging.
I have shared my own information plus a variety of public information concerning challenges with health related issues; diagnosis, various neurological disorders, medications, treatments, medical professionals, support, events & stories from others online, & more.
I also shared a special letter in 2013 from my husband, Steve, when he had wrote his views about our story, our life situation. I just read it the other day & thought it was worth sharing again.
I am forever thankful Steve is my rock & I am so lucky we found each other ❤️

Address

London, ON

Website

http://www.zazzle.ca/T_Alderson, https://www.canadahelps.org/en/charities

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