Kelowna, I’m bringing some Parkinson’s yoga and Time Out for Caregivers to you!

After spending 4 years in Kelowna completing my PhD, the Kelowna PD community is near and dear to my heart! Just ask about 70 of them about getting hooked up with an EMG machine and spending the day being monitored… I definitely couldn’t have done my PhD without them!

… that’s why I’m coming back to Kelowna and bringing some yoga with me. Friday November 15th and Sunday November 17th I’ll be running two yoga workshops specific to PD at Trinity Yoga Center (#6 – 3818 Gordon Drive).

Space is limited, so please register early by sending me an email (kaitlyn.p.roland@gmail.com) or calling me at 250.589.2046

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I’m also in town for a Parkinson Society BCTime Out for Caregivers!” Event on November 16th from 1-4pm… so care partners, come join me for discussions on self-care and resilience!

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… can’t wait Kelowna! much love.

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self-care

The Parkinson Society British Columbia (website here) has a much needed initiative this year to support workshops for caregivers of persons with Parkinson’s disease,

Time Out for Caregivers.

Lonnie Ali caring for her husband, Muhammad, who has Parkinson’s disease

I was asked to be the keynote speaker at their second workshop in Kelowna on May 26th and was so honored to be able to share the afternoon with these amazing men and women.

I was able to relay to the participants about the importance of their health and how there are buffers that reduce caregiver burden, especially :

  1. being prepared to be a caregiver
  2. fully accepting and finding meaning in the caregiver role, and
  3. establishing a quality relationship with the person you are caring for
The main cause of PD caregivers burden is not always the physical tasks they have to do, for example helping a person in and out of bed, feeding, more household chores, etc., but the mental worry… about safety of their spouse or if they have to make big decisions alone, like when to sell the house and/or move into assisted living, legal powers of attorney, etc.

when your direction in life changes… http://www.cartoonstock.com

Some of the information I hoped to convey was that caregivers need to care for themselves!
  • Don’t suffer and try to set boundaries, if there’s a task that’s too much or something you don’t want to do – ask for help! find support! If you need some “me-time” or “me-space” create that. Be assertive! This may involve finding your voice or an advocate.
  • Don’t give up on activities you like to do! Modify so you can still keep active and interested in life together… remember the disease doesn’t define you!
  • Sustain yourself… caregivers are like lifesaving equipment, you don’t want to burn out. It’s like when you’re on an airplane and you are support to put YOUR oxygen mask on before helping others.

  • find someone that can cheer you on and lift your spirits… and don’t forget to celebrate all the small joys. The facilitator for the Kelowna Parkinson’s support group tells everyone to write down THREE things you are grateful for everyday. Doesn’t matter if they are big, small or inbetween! Then, at the end of one year you will have over ONE THOUSAND things to be grateful for… pretty amazing, eh?

check out this novel that chronicles gratitude by Ann Voskamp

I understand this is easier said then done, but getting caregivers to focus on self-care is a great start! I am so grateful for the participants who attended the workshop and to the Parkinson’s Society for starting this initiative, you can contact them at: info@parkinson.bc.ca for further information. A copy of my presentation slides are available by clicking here… please share!


and this is not only applicable to PD caregivers, but everyone…when was the last time you checked in with yourself to see how you were really doing? much love.