Posted in Blog posts, COVID-19, Fibromyalgia

Even #COVID19 Can’t Beat Our #LdnOnt Spirit!

We are living in unprecedented times. Now more than ever we need to be here for each other. Please help spread the word by sharing this post on: Twitter, Facebook, Pinterest, any or all social media platforms. Also, please, tell other Londoners (London, Ontario, #LdnOnt) about this – by text, phone, email, Facetime, Zoom, Skype, snail mail – anyway you can share the gratitude for those essential workers who are putting their lives on the line so we can stay safe! Even COVID-19 can’t beat The London Spirit! Share the gratitude! Thank you!!!

Dear Londoners!
Several grassroots-led, community-wide efforts are underway hoping to lift and keep morale among Londoners high, especially front-line healthcare and essential service workers, during this extraordinary time in all our lives. Please join us in saying “Thank You” to those putting their lives on the line for us. You can participate through a number of ways explained below, to demonstrate your individual/group support, express gratitude, and cheer on these workers for as long as it takes.

Here’s a few ways in which you can support your neighbourhood, your London community, your friends, and neighbours:

1. Window Signs – Here are some signs you can print in colour or black & white, or get creative, make your own, heartfelt “Thank You” signs. Display these signs in your front windows, mailbox, front door, fence, railings, tress, garage door, etc.  You can also spread the word by printing then inserting into a sheet protector, and placing on the sides of the Canada Post postal boxes or to the poles of street signs (just like you would display garage sale signage) – please be careful to damage anything.  Print and put them up for the duration of this crisis in London!

2. Hearts in Windows – Children and adults alike can have some fun drawing, painting and/or cutting out hearts in all colours and sticking them in your front windows as another way to express support to front-line workers. There is a nationwide movement, originating from British Columbia, calling on all Canadians to participate in this activity.

3.Ribbons – Tie RED RIBBONS around the trees and shrubs in your front lawn, fences, railings, the front of your apartment building (with permission), on the tree trunks of the trees along your street. That way those who are required to go into work during these challenging times know “you have their back”.  Why red? The colour red symbolizes courage, strength, confidence, compassion and love – all things we want and wish for our front-line healthcare and essential service workers!

4.Facebook & Twitter – we have set up a new community page, The London Spirit – Covid19 Crisis or @thelondonspirit, and a Twitter account, @londoncovid19, which are both safe, open social media spaces for anyone to post…

Messages of hope! Messages of gratitude! Acknowledgement of essential workers. Sharing positive stories. Sharing inspirational stories of how specific front-line healthcare and all essential service workers have helped you, your family, organization, neighbourhood, etc. during this contagious and dangerous pandemic. Please, please, please share tales of courage and/or kindness by our local heroes: healthcare workers, grocery workers, pharmacy workers, store clerks, maintenance workers, bus drivers, public service workers, and everyone working so we can stay safe at home! Please, feel free to express your expressions of gratitude, motivation and encouragement to front-line healthcare and all essential service workers!
EVERYONE, please take a few minutes of your time to participate in one or more of these easy-to-do, inexpensive, grassroots, community-driven activities! They can help boost the morale of so many who fear for their own families, but are serving Canada by going into their workplaces everyday, in spite of the risk to themselves.  
Let’s demonstrate how STRONG and ALIVE our community spirit, The London Spirit is by participating  in all of these activities TODAY.  Now, more than ever, we’re all in this together, so let’s support those risking their lives to save ours!

Even COVID-19 can’t beat The London Spirit!

https://www.facebook.com/thelondonspirit/

Posted in Blog posts, Fibromyalgia

Now I Wanna Feed Your Dog?

Tomorrow is the first day of Spring so here’s a simple, no-bake recipe that’s sure to please everyone who is #Stayinghome to help everyone stay well. This is a tough time for everyone and those with chronic illnesses are vulnerable. For the safety of our members we’ve cancelled all Fibromyalgia London Group activities, for now, but that doesn’t mean we can’t still connect!!! Here are some ways to connect! Here on the blog https://fibrolondongroup.ca/ ; and/or on Twitter @fmlondongroup ; and/or on Instagram @fmlondongroup ; and/or on Facebook @fmlondongroup ; and/or via phone: 519-453-3198 , and/or text; and/or Skype/Facetime; and/or Netflix Party (on Chrome); and/or email fmgroup.london@gmail.com  or darcyyada@gmail.com. And here’s a fun, simple way to pass part of the day. This is one of our family favs, it might be yours too! My paternal Grandmother named it “Dog Food” (when you’re in the process of mixing, you’ll know why) and we’ve kept the name.

Ingredients: 45 choc wafers (approx 1 package if you don’t snack, I mean, who would do that, just grab a cookie and start munching away…er, anyway) – this is another recipe where you can substitute other cookies, but they must be tap-on-the-counter-hard or frozen; 1/2 package of mini marshmallows; 1 cup coconut (sweetened or unsweetened, but you know which tastes better) and 1 can Eagle Brand or other condensed milk. Wash your hands.

Crush wafers/cookies in a bowl; I’ve always found the bottom of a cup or potato masher works well. Then mix in marshmallows, add the condensed milk and stir well (there it is, now you’ll understand the name, “Dog Food”). Butter 9-inch pan, then sprinkle coconut on all surfaces of the pan so it sticks to the buttered sides/bottom. Spread the mixture evenly. Then sprinkle the remaining coconut on top and press it all down together. Seriously, that’s it, it’s done! Cover well. Place in fridge for a few hours, then, try (I triple dog dare you!) not to eat it all before giving it away. It also freezes beautifully, but really, how often will you have any left to freeze?

#StayHome #SafeHands #WashYourHands #StaySafe (from COVID-19 and everything else too!) and Enjoy!

Posted in Blog posts, Fibromyalgia, Getting social

“C” is for Cookie, That’s Good Enough For Me

“I want to take all our best moments,
put them in a jar, and take them out like cookies
and savor each one of them forever.”
~ Crystal Woods

Do you have fond memories of smelling cookies baking?
Do you drool when you think of that first bite of a cookie?
Do you remember the seasons by when Girls Scouts sell cookies?

Don’t let people make you believe that you have a cookie “problem” or a cookie “addiction”, it’s simply #cookielove.

“Count your cookies, not your problems.”
~ Cookie Monster

“C” is for Cookies, That’s Good Enough For Me
(and the Cookie Monster, a role model for some).
If you’re trying to kick a cookie habit love,
then stop reading right now!
Warning:
Do Not Read Any Further!
What’s coming up next
can not be unseen!!!

The first bite of these cookies and you won’t know whether to thank or curse (or both), Lynn, an amazing, kind, and supportive Peer Leader/member of the Fibromyalgia London Group, for introducing you to these delicious, mouth-watering morsels. I thank her, but my waist may not. Where’s that button to stop “cookie” pop-ups?

This simple (read, not too tiring) yet magnificent recipe has been used as a staple cookie recipe in Lynn’s family since 1980’s. Based on a Canadian Living Classic recipe from her first cookbook as a young wife and mother, this recipe proves that simple can be best.

“Home is where heart is. Heart where cookie is. Math clear: Home is cookie.” ~Cookie Monster

Ingredients:
1 cup butter
1/2 cup packed brown sugar
1 egg
2 tsp vanilla
1 1/2 cups all purpose flour
(or your choice, or gluten-free flour)
1/2 tsp baking soda
1/2 tsp salt
1/2 tsp cinnamon
1 1/2 cups rolled oats

Raisins, seeds, cranberries,
and/ or chocolate chips optional
(when is chocolate ever optional?)

Preheat your oven to 350 (180C)

In a large bowl cream together butter and brown sugar.
Beat in egg and vanilla.
In separate bowl mix your salt, baking soda, cinnamon and flour.
Add together and blend into a creamy mixture.

It’s a very versatile batter, sometimes
Lynn adds both chocolate chips and raisins
(and sometimes white and dark chocolate chips)
but you could also add nuts, dried cranberries,
pumpkin seeds, sunflower seeds…if so desired.

On a well-greased cookie sheet (or parchment paper or non-stick), make little mountains of dough (approx. 1 tsp), leaving about 2 inches between cookies. Flour the bottom of a glass and gently flatten each cookie to about 1/4 inch thickness.

“Early bird gets the worm. But cookie taste better than worm. So me sleep in.” ~ Cookie Monster

Bake for about 8-9 or until golden brown. Let them cool down on a baking sheets for about 2 minutes (if you can wait that long without eating one, for testing purposes only, of course) then remove to baking rack to cool completely. Makes about 40 cookies.

This recipe can be kept for a few days in sealed container and can be frozen for up to a month (either the baked cookies or the dough)….if they last that long.

What’s your favourite cookie or cookie recipe? Share the cookie love by sharing this on: Instagram, Facebook, Twitter, etc. and/or in the comment box below and/or email to me (D. Parker – Mom, blogger https://yadadarcyyada.com/ , silliness coordinator, Peer Leader/ member of FLG and cookie addict lover): darcyyada@gmail.com I should have warned you, dear readers, that this website uses “cookies”…Nom Nom Nom!

“No cry because cookie is finished. Smile because cookie happened.” ~Cookie Monster

Posted in Blog posts, Fibromyalgia, Guest Speaker

IT’S NOT ALWAYS EASY: COPING TIPS FROM PSYCHOLOGY

Dr. Rhonda Gilby is a blogger, member of Fibromyalgia London Group and the mother of two daughters with Fibromyalgia. Dr. Gilby has been a clinical psychologist for over 30 years, helping people cope with the various problems that they are experiencing. She has taught psychology courses at Western University and its affiliates, worked with troubled children, and provided psychological counselling to University students. Dr. Gilby recognizes that “it’s not always easy” and writes about how findings and ideas from the field of psychology can be applied to help everyone to cope better in their day-to-day lives. ngilby@rogers.com

Savouring the positive – where are you shining your flashlight?

Our lives are filled with many, many different experiences. At any given time, there can be many wonderful things going on in your life, at the same time as you are dealing with some “not-so-wonderful” things.  What do you focus on?

Imagine that you live in darkness, always holding a flashlight in your hand. Where do you shine that flashlight? How much of your time do you spend focusing on the negative, shining your flashlight into a dark corner where some unpleasant experiences or painful feelings reside, and how much of your time are you using your flashlight to search for and focus on the happier, more pleasurable things that are also happening for you right now.

Life can (and will) hit you with all kinds of challenges and disappointments. Nobody gets a perfectly smooth ride on their journey through life. But you do have some choice in how those setbacks will affect you. You can take control of your flashlight, and redirect its beam to the delightful things that are also around you, despite those challenges, and focus on the richness that your life also offers.

bumpyroad

Choose to savour the small pleasures that life offers – making a deliberate effort to notice and appreciate the positive aspects of life. Psychologists Fred Bryant and Joseph Veroff have explored the concept of savouring, noting that we sometimes we can experience positive feelings or experiences in our lives, and be too busy or too wrapped up in our negative emotions to pay much attention to them.

Happiness isn’t just about having the positive experiences, it’s also about noticing them, enjoying them, trying to prolong them, shining your flashlight on them. For example, rather than eating your morning muffin mindlessly, linger over it, appreciate the aroma, the sweetness or crunch, the blueberries as they burst in your mouth. 

blueberry muffin

Rather than just walking to get from A to B, notice the warmth of the sunshine on your face, feel the crispness of the air, or observe the beauty of the clean, white snow on a winter’s day.

Riverside walk on a snowy winter's day Stock Photo - 4218141

Instead of feeling like you really didn’t do anything tonight, even a quiet evening with family or friends can be savoured, for the comfort, calm, and feeling of care that it provides. If you make the effort, there is lots of positive in every life to focus on. You can savour a memory of a past experience, savour an experience as it is happening  or look forward to an anticipated enjoyable future experience.

Remember that good moments pass quickly, so make an effort to consciously appreciate them, and be careful about where you shine your flashlight.

Take care and be good to yourselves.

Dr. Rhonda Gilby, guest blogger, member of Fibromyalgia London Group. teacher, clinical psychologist for over 30 years, and the mother of two daughters with Fibromyalgia.  ngilby@rogers.com

Posted in Blog posts, Educational, Fibromyalgia, Getting social, Guest Speaker, Sharing Circle, Social events

Happy New Year 2020! What’s Next?

Happy New Year! Hard to believe it’s already 2020 (no vision jokes). A new year (and a leap year at that), a new decade, but what’s next? Sometimes when we’re in a Fibro flare, stressed out, and/or having a rough time, it’s hard to think, what’s next? So make plans anyway, make choices, don’t let the world make them for you.

Here at Fibromyalgia London Group we understand, the holidays can add extra stress (https://fibrolondongroup.ca/2019/12/15/12-unusual-ways-to-relieve-your-holiday-stress/) and post-holiday exhaustion is real…and don’t even get me started on what winter does to Fibro.

So come out to some (or all – with a $20 membership per year every single event, program, sharing circle, everything is no extra charge to you and a registered caregiver/supporter/loved one) of our programs, events, sharing circles, etc. – relax, de-stress, learn about resources and ways to cope with pain, exhaustion, anxiety. Also, you’ll meet folks who know what you’re going through. We don’t just say we get it. We get it.

Please note: Fibromyalgia London Group (FM/CFS/chronic pain) Saturday Sharing Circle sessions in the North end, North London Optimist Centre will now be bi-monthly (every second month, 6 times per year). As well, the FM/CFS Caregivers’ Support Group, led and facilitated by Rick Avdovich. Caregivers, supporters, and loved ones of persons living with FM or CFS have their own support circle, held Bi-monthly (every 2nd month/ 6x/year) at the same time our FM/CFS/CRPS/ME Sharing Circle meets.

Thursday Sharing Circle sessions will continue MONTHLY. So just as a reminder, there’s NO Sharing Circle January 4th, but join us at the North London Optimist Centre January 11th, 2020 for an educational opportunity…

LIVE BLOOD MICROSCOPY Saturday, January 11, 2020; 1-3pm North London Optimist Community Centre.

And Thursday January 16th for a Support/Sharing Circle. Free parking and on several London Transit routes, ie. #10 – check out http://www.londontransit.ca/plan-a-trip/routes-schedules/ for more details. Also, the City of London has an income-related bus pass http://www.london.ca/residents/social-services/discretionary-benefits/Pages/Subsidized-Transit.aspx Whichever way you arrive, we want you to thrive!

Thursday support sessions are still monthly, in January 2020 it’s Thursday January 16th, 2020 11am-12:30pm (doors open at 10:30am and Peer Leaders will be there to answer questions, sign up members, share resources or just to listen) – Earl Nichols Recreation Centre 799 Homeview Rd. 11am-12:30pm. Free parking and on several London Transit routes, ie. #10 – check out http://www.londontransit.ca/plan-a-trip/routes-schedules/ for more details. Also, the City of London has an income-related bus pass http://www.london.ca/residents/social-services/discretionary-benefits/Pages/Subsidized-Transit.aspx Whichever way you arrive, we want you to thrive!

Knit Happens: Therapeutic Knitting for all! Bi-weekly knitting program, 3rd Floor Board room London Public Library Central Branch (accessible to all). Please remember all FLG events are scent-free please. Instructor Janice Sumpton shows how knitting can help with chronic pain, or everyday stress, because Knit Happens! All are welcome! Open not only to Fibromyalgia London Group members but to the general public. New to knitting or an expert, come to learn or just for the company! Free 2hr parking (validate at front desk of LPL with library card) and on several London Transit routes, ie. #4, 6, 13, 90, and more – check out http://www.londontransit.ca/plan-a-trip/routes-schedules/ for more details. Also, the City of London has an income-related bus pass http://www.london.ca/residents/social-services/discretionary-benefits/Pages/Subsidized-Transit.aspx Whichever way you arrive, we want you to thrive! January 9th 1pm-2:30pm – bring your needles and yarn – we’re going to have a ball!

Cards and Company Monday Afternoons! January 13th & 27th, 2020, 1pm-3pm!!! Free for Fibromyalgia London Group members and a supporter/caregiver but snacks are always welcome!!! Free parking and on several London Transit routes, ie. #4, 6, 90, 13, 15 and more – check out http://www.londontransit.ca/plan-a-trip/routes-schedules/ for more details. Also, the City of London has an income-related bus pass http://www.london.ca/residents/social-services/discretionary-benefits/Pages/Subsidized-Transit.aspx Whichever was you arrive, we want you to thrive! We’re playing with a full deck (honest)!

Please read and keep checking back, to the homepage, https://fibrolondongroup.ca/ changes all the time with upcoming events. To the right of that page, under “What We’ve Been Up To” are blog posts about events, Fibromyalgia and other stuff. Also, and very important, please share this homepage https://fibrolondongroup.ca/ for the London Fibromyalgia Group (FLG) with family, friends, colleagues, medical professionals, clubs, groups and on especially social media – you never know when you’re going to help someone. Then please, submit…

ORIGINAL content (written by you) blog posts, memes, quotes, ideas, recipes, lyrics, personal experiences, etc. to: iwanttobelieve@rogers.com (you can use your first name, full name, pseudonym, whatever you feel comfortable with, in the blogging world, anything goes…). Here are a few examples of ORIGINAL blog posts, but the whole point of original is you do you!!!

“Chronic Suckage”, “Is #Fibromyalgia Still a Four Letter Word?” and “12 Unusual Ways To Relieve HolidayStress” by Guest Blogger, D. Parker https://yadadarcyyada.com also a member of Fibromyalgia London Group and a Peer Leader.

Keep checking https://fibrolondongroup.ca for more and more details. Even if no one else understands, we do. New Year, new you or are you enough already and just need some help to live your best life? Don’t wait for help to come to you, come to us for help. Fibromyalgia London Group
Tel: 519-453-3198 ~

Email: fmgroup.london@gmail.com 

~ Website: www.fibrolondongroup.ca

Happy New Year and hope to see you soon!

Posted in Blog posts, Fibromyalgia

12 Unusual Ways To Relieve Your Holiday Stress

12 Unusual Ways To Relieve Your Holiday Stressby guest blogger, Fibromyalgia London Group Member and Peer Leader, D. Parker (https://yadadarcyyada.com)

The holiday season stresses out most everyone, but for those who are ill, the holidays can be a nightmare (before and during Christmas); it’s stressful for even those who don’t celebrate Christmas (or try not to celebrate).

The roads are busier.
Malls overrun by zombies (We are The Walking Dead, but with brightly-wrapped gifts).
Christmas songs drone on, but peace on Earth, really, there’s barely a pretense of civility.

So many Santas, ringing and ho-ho-hoing for money to buy toys – I thought there was a workshop and elves for that

Expectations.
Unrealistic expectations.

Too much food (First World Problem).

Frolicking.
Accidents.
Frolicking accidents.
Ugly Christmas sweaters (no longer ironic),
now ironically iconic?

Gifts/gift cards/e-gift cards,
“the perfect gift” for the “perfect” Christmas –
that’s where stress-relievers come in.

First, take a deep breath. Christmas is one day. One. 24 hours. 1440 minutes. Let’s also enjoy the other 364 days in the year. Relax.

Second, the holidays should be about: giving, helping, hoping, kindness, compassion, and dreams; not pushing, whining, complaining, stressing and screams…Relax.

Third, you need to find out what works for you, what makes you happy, what brings you comfort and joy. If you don’t know that, how can you share it with others? Relax.

Here are some usual ways (and unusual, whatever that means) ways to relieve stress during the holidays (and all the year through)? There are more than 12 so you decide which is which.

If I’ve left some out and I’m sure I did, please comment to tell me what I missed and then share the post on social media so others can tell me what I missed as well…

  • Read books/ebooks (This is a safe space, no “books vs ebooks” arguments here; all books are welcome and accepted!).
  • Progressively relax.
  • Dog/Cat/Fish/Pig/ Pony/Ferret/Bird/Horse/Frog therapy.
  • Volunteer (I once knew someone who said more people would volunteer if they were paid, ummm, that’s a job).
  • Write a blog/journal/novels/poems.
  • Manicure/Pedicure (at home works too).
  • Bake (me a cake?).
  • Aromatherpy (Don’t limit yourself to the usual scents, whatever smells good to you, smell away).
  • Look for the Fibonacci symbol in nature or fractals, so fun on snowy days.
  • Design clothes. Wear clothes. Buy New-To-You clothes (Goodwill, Talize, Salvation Army, Value Village, Mission Store, and other Love-Them-Again stores are awesome).
  • Go see a play, be in a play, write a play, direct a play.
  • Bike.
  • Golf/Mini Golf.
  • Look at the stars (the ones in the sky).
  • Plant yourself near a plant to reduce your blood pressure.
  • Sleep/Nap/Rest.
  • Karate (relaxed and ready to defend yourself, probably not against Ninjas or aliens, but maybe zombies or vampires).
  • Visit an art gallery/museum.
  • Hike.
  • Do chores/Clean.
  • Stream (Netflix, Amazon Prime, Hulu, Apple TV, Disney Plus, Acorn TV, Crave, HBO, TMN, SlingTV, BritBox, and many more (with more popping up every day).
  • Bowl.
  • Curl.
  • Url.
  • Unfurl.
  • Play board games.
  • Play video games.
  • Play card games (Fibromyalgia London Group has an afternoon of cards and company once per month, join us).
  • Learn something…anything.
  • Travel/Stay and enjoy.
  • Paint.
  • Garden.
  • Do puzzles – crossword, boxed puzzles, puzzle boxes, find-a-word (Have you heard? The bird is the word), sudoku, logic, trivia and if you can figure out people, wow, you’ve solved the biggest puzzle ever.
  • Apply gentle pressure to the spot between your 2nd and 3rd knuckle, between your fingers, where your finger and hand meet to reduce stress.
  • Weave.
  • Camp.
  • Glamp.
  • Dance.
  • Cheer someone up with a fun surprise (Do not break into their home and draw a happy face on the wall or anything in red lipstick on their mirror, apparently that’s considered “creepy”).
  • Craft.
  • Raft.
  • Wine/Beer tasting tour (Don’t taste and drive).
  • Learn some magic tricks (Be nice to rabbits).
  • Get/give a facial.
  • Sing.
  • Watch the clouds (the ones in the sky).
  • Jump (jump jump jump around) on a trampoline (safety first).
  • Swim (just keep swimming, swimming, swimming).
  • Smile (I just like to smile, smiling’s my favourite).
  • Drink water (don’t waste it).
  • Draw.
  • Create the next big fad! i.e. Lint kittens and puppies. Easy to keep – no walks, no food, soft and cuddly, and easy to house-train. Do not expose to water.
  • Ski.
  • Sauna.
  • Snowboard.
  • Snowshoe.
  • Walk.
  • Run/Jog/Sprint.
  • Quilt.
  • Be mindful.
  • Plant trees.
  • Join a team (fantasy or real).
  • Pet sit (don’t actually sit on a pet).
  • Dream.
  • Tear paper (then recycle then tear again).
  • Visualize (guided or unguided, just remember to leave some breadcrumbs to find your way back).
  • Crochet.
  • Pay it forward.
  • Help.
  • Be kind (random or deliberate).
  • Fix stuff (fix something for someone: TV, car, fridge, cellphone, alarm system, computer, appliances, sewing machine, etc. Even it wasn’t broken, er, at the time, they’ll probably understand you were trying to give them a gift…probably).
  • Upload/download/unload.
  • Meme.
  • Give your time.
  • Offer your knowledge.
  • Give your full attention.
  • When a child hands you a toy phone or a banana, answer it and have a conversation (best time with a phone/actually smart).
  • Take a shower (not at the Bates Motel).
  • Take a bath (not in a horror movie).
  • Enjoy social media for what it is not what you want it to be (because the internet).
  • Take some photographs (not just of your food and selfies with duck lips).
  • Skate.
  • Mentor someone.
  • Review something.
  • Ski-doo (not on thin ice…it’s all going to be thin ice soon).
  • Watch a sunset.
  • Watch a sunrise.
  • Cook (Combine food and fashion ie. Forget Lululemon, how about lasagna leggings? Pizza pants. Taco ties. Chocolate crop top. Wine wedding dress. Turkey tux. Beer boots. Hamburger hat. Curry coat. Steak scarf. Bacon blouse. This food fashion can be consumed at any time – hopefully not when you’re out in public).
  • Join a club (not a gang).
  • Drink green/white tea.
  • Inspire.
  • Be inspired.
  • Organize.
  • Walk in a park or the woods (not at night on a full moon, just in case).
  • Climb a wall so you don’t climb the walls.
  • Hug.
  • Laugh.
  • Laugh some more.
  • Make someone laugh.
  • Spend time with nature and animals (don’t pet grizzly bears, badgers, or snakes, start slow with cats, dogs, rabbits…then move up).
  • Build a snowman (do you wanna?).
  • Remember.
  • Forget.
  • Remember to forget.
  • Smash stuff (smash plates, bowls, walls, pumpkins,etc., and if you can’t go to one of the places where you pay to smash stuff, I’m sure family and friends will understand you need stress relief, especially during the holidays).
  • Hope.
  • Make soap not dope.
  • Elope.
  • Pop corn.
  • String popcorn.
  • Visit (real or virtual as long as you’re there, in the moment).
  • Yoga.
  • Watch TV (question what you watch).
  • Go see a Movie (question what you watch).
  • Listen to someone.
  • Breathe deeply.
  • Be grateful.
  • Chop wood.
  • Woodworking.
  • Carving.
  • Tis the season, cut down a Christmas tree for a busy family member or friend. Cautionary note, unlike in the Hallmark and other Christmas movies, cartoons, etc., apparently it’s “frowned upon”, some might even say “illegal”, to just randomly cut trees down. Who knew?

One of the best ways to relieve stress, being honest, with yourself and others; we/they/me/whoever may not appreciate it at first, but it could be the best gift ever, someday.

 Chocolate. Enough said.

If you know me and/or you’re a reader of my blog (https://yadadarcyyada.com) you know, I think laughter is the best medicine and it certainly qualifies as a stress reliever. Laughing, even if it hurts sometimes, still makes me feel better. I go to a happy place, including but not limited to: Psych, George Carlin, Seinfeld, Community, Friends, Rick and Morty, The Office, Marx Brothers, Flight of the Conchords, and more.

I love to share the laughter. If I can make someone smile, laugh, giggle, chortle, spew liquid from their nose, then hey, I feel better. Get silly. Adulting is tough, who says we can’t be a kid at heart?

Finding ways to help others is a great stress reliever. It’s hard to think about your problems when you’re helping others with theirs.

There are an endless amount of causes out there, try to support those who really need it. Those who are hungry, scared, without shelter, without hope, being abused, ill, falling through so many cracks.

Donate to a cause in someone’s name instead of handing them another gift they may or may not need or want, or better yet, start a foundation in their name, I’m sure it won’t affect their taxes…much. Help yourself by helping others.

What else would be good for relieving your tension? I’ve recently learned (perhaps a slight exaggeration) to knit thanks to the kind and very patient Janice Sumpton, who has been knitting for decades (discovered the therapeutic aspect when diagnosed with Fibromyalga. Here is her wonderful presentation, take the time, it’s worth it 2019TherapeuticKnittingFMgroup Firefox was being tricky, but it opens easily w/ Chrome and Adobe Acrobat Reader).

With the cooperation of Fibromyalgia London Group (FLG) and the London Public Library Janice teaches/hosts a bi-weekly knitting class, everyone is welcome, it’s free (that is a real word, look it up) and open to all levels of knitting, I’m clearly a great example of that.

And in 2020 we’re also going to add knitting to help others.

Absolute beginner? Knit for fun? Want to knit more? Want company? Are you a knitting genius and can knit your own spaceship? This may be for you.

New projects? As a newbie my projects were: knit a black cable knit sweater and a Doctor-Who-vintage-Tom-Baker-as-The-Doctor scarf. I’ve been talked down to scarf of one colour for my first project). Or UFOs (Unfinished Objects/Projects)? Bring them in, knit, chat, trade ideas, laugh, enjoy.

Turns out knitting can be a “knotty” stress reliever.

Exercise is suggested for stress relief, but with pain and fatigue, exercise can be challenging. Years ago, someone suggested Tai Chi for Fibromyalgia/relaxation/arthritis/exercise, I thought, how would flailing my arms around, slowly, help with any of those things? I’ll just look weirder than I usually do.

I reluctantly tried it. It saved my life, at least, my quality of life. Tai Chi, a few times per day; in the morning to relax from sleeping – Fibromyalgia patients will understand https://yadadarcyyada.com/2019/11/22/99-problems-and-fibromyalgia-is-all-of-them/ https://fibrolondongroup.ca/2019/12/06/chronic-suckage/  

Lifting weights? I’m no Schwarzenegger, but Hasta la Vista, babyweight (my son is in his 20s). I like Yoga (and Baby Yoda), but it can be painful. Walking helps, but my dogs start barking and the rest of my body growls at me.

I love swimming (not so much Aquafit), but getting there and back, dressing, undressing, showering, etc. is exhausting; I sometimes feel worse, certainly less relaxed (and it’s pricey). 

What else? For seniors, VON offers free programs twice a week, (SMART) Seniors Maintaining Active Roles Together; there’s Ageless Grace (more like Graceless Aging for me). I’ve tried the gym. Belly-dancing (don’t try to picture it). Dancing (Frankie says Relax).

Yet I stick like glue to Tai Chi because it unsticks me. Relaxes. Soothes. Feeling sore? Tai Chi won’t magically fix everything, but it helps ease some aches and gets you moving.

To learn Tai Chi I borrowed items from the London Public Library (having fun isn’t hard if you’ve got a library card). Later bought VHS tapes (yes, that long ago, I fought off a saber-tooth tiger to get home), then DVDs (now on YouTube and streaming services, soon to be uploaded into our brains). 

Another option, classes, i.e. Phoenix T’AI CHI Centre ( www.phoenixtaichi.ca or Info@phoenixtaichi.ca or 519-872-2408) offers T’AI CHI for Health Challenges, geared to complex health issues including but not limited to: Fibromyalgia, Chronic Fatigue Syndrome as well as other pain and mobility issues with Terry Lynn Clarkin (also a member and Leader of the London Fibromyalgia Group).

Phoenix T’AI CHI also offers an Introduction to Sun-Style T’AI CHI (Dr. Paul Lam’s Tai Chi for Arthritis and Fall Prevention Program). 9-week program starts January 16, 2020 (I have a feeling 2020 is going to be a year that calls for a lot of stress relief!) with the wonderful Terry Lynn Clarkin.

Now I have fun with it, I pretend I’m carrying an invisible jar containing invisible chocolate, so I must guard it with my life, but seriously, once I opened my mind, body and heart to Tai Chi, it gave me a priceless gift – some pain and stress relief so I could have quality of life.

Disclaimer: This blog post is not an advertisement nor is it in any way meant to provide medical advice. It is intended for informational purposes only. It is not a substitute for professional medical advice, diagnosis or treatment. Never ignore professional medical advice in seeking treatment because of something you have read on the internet, or in a book, or heard from family, friends, groups, etc. Any exercise or exercise program is not without risks, even for healthy individuals, please consult your physicians(s) before starting, changing and/or increasing any exercise or exercise regime. You are responsible for your own health and safety at all times. If you think you may have a medical emergency, immediately call your doctor or dial 911. Information is gathered and shared from reputable sources, however, Fibromyalgia London Group (FLG) is not responsible for self-diagnosis, noncompliance, omissions, self-treatment, or errors.

Wishing everyone a safe, happy and stress-free (ok, low stress/reduced stress) holiday season: Happy Holidays! Merry Christmas! ¡Felices Fiestas! Jie Ri Yu Kuai! Laethanta saoire sona! Happy Hanukkah! Joyous Kwanzaa! Yuletide Greetings! Best wishes for 2020! Joyeux Noël! Let it snow…somewhere else! Feliz Navidad! Seasons Greetings! Happy New Year Joy! Celebrate! Be merry! Shiawasena kyūjitsu! Boas Festas! Li holide eximnandi! Happy Christmas! Happy New Year! Wishing you a latke fun this Hanukkah! Hau’oli Lanui! मेरी क्रिसमस ! Forhe Feiertage! Selamat Hari Raya! Happy Channukah! oyeuses Fêtes! Prettige Feestdagen! Buone Feste! Trevlig Helg! Jingle All The Way! Happy Holidays from owl of us! Tis the Season! Warmest greetings! Happy Holidays, Mate! It doesn’t matter how you say it as long as it’s said with kindness.

Remember, getting through one day (for example, Christmas Day) isn’t the same as finding and giving joy each day. What about you dear readers? What are some of the usual or unusual ways you know to relieve stress during the holidays and all the year through (remember this is a more or less family-friendly blog).

Opinions are that of the author and do not necessarily reflect the views of Fibromyalgia London Group.

Copyright D. Parker (Donna Parker/yadadarcyyada) c2019

Posted in Blog posts, Fibromyalgia

Is #Fibromyalgia Still a Four Letter Word?

5 years ago I wrote, “Fibromyalgia is a Four Letter Word” https://yadadarcyyada.com/2013/08/08/fibromyalgia-is-a-four-letter-word/, and now, 5 years later, I’ve updated it and I think, sadly, it’s still true, tell me what you think.

Guest blog by D. Parker, blogger at https://yadadarcyyada.com/ also a Fibromyalgia London Group member and Peer Leader.

This isn’t meant to be whiny (see how that goes…), or a ‘it can be fixed’, or whatever blog post. Just a few thoughts about why people think Fibromyalgia isn’t a real syndrome, that it’s just lazy, unmotivated people and mostly, why I don’t have answers.

Let’s begin at the end…I don’t have all the answers, maybe because I don’t sleep enough. Also, I’m not a million years old. In addition, I’m certainly not a super genius.

Oh, did I mention I don’t sleep enough?

People prefer to think people with disorders/syndromes such as Fibromyalgia are lazy, I dunno, maybe because they don’t want to accept that they could wake up one morning and have something like: Fibromyalgia/Fibromialgia, Chronic Fatigue Syndrome, CRPS, ME, Lyme Disease and/or another chronic illness.

Instead of doing the whole “there-but-for-the-grace-of-God-go-I” thing, too many people just decide that people with these illnesses/syndromes could do better if they only: weren’t so lazy, would exercise more, ate differently, got a better attitude, tried harder, did more, pushed themselves, pushed through, pushed harder…

It’s easier to believe that, I suppose, than believe someone who was full of energy, productive, happy, motivated, etc. can too quickly become a person: full of pain, fatigued (relentless insomnia and pain can tire you out a wee bit),

frustrated, sad (so many sadz),

depressed, anxious,

plagued with memory issues,

exhaustion, confusion…

have massive struggles to function, and so on.

Fibro becomes a joke, a stain, a dirty word because otherwise people would have to accept the reality that people get sick. Humans get sick. They get short-term illnesses, they get injuries that sometimes heal and sometimes, don’t, they get chronic illnesses, they get terminal illnesses, and some live with agony and sometimes, they die.

People often tell someone with cancer they should fight The Cancer, as though that will fix everything. Yes, poking a toothpick at a dragon works so well. Ever thought of how that makes people feel, when they’ve lost a loved one to cancer? Oh, so my loved one just didn’t fight hard enough, well, thanks, that makes me feel so much better.

The same goes for those who’ve lost a loved one to suicide. I’m sure they feel horrible enough without others implying their loved ones gave up, chose to leave, didn’t love them enough to stay, weren’t strong enough, or just didn’t fight hard enough. 

I don’t live in someone’s head so I can’t say if they tried, if they fought, or if they chose, but neither does anyone else, so no one is qualified to make these judgmental statements. No one. Live your own life and let other people live theirs.

Instead of mocking someone with an illness, try having empathy for them. Not sympathy or pity. Compassion. Kindness. I’m sure there are some bizarro individuals would prefer to be ill than well (but they have a whole other illness), but come on, does anyone, anyone at all truly, deep in their heart of hearts seriously believe that’s a majority?  Most people would choose to be well.

Most people would choose to have a full life, a life with a normal amount of pain and fatigue and other symptoms. Just like most people would choose to beat cancer. Hell, most people would choose not to get cancer at all. Most people would choose not to have a mental illness. If there was a choice involved.

People are slowly coming around to the belief that people who lead a homosexual lifestyle didn’t choose to be that way, it’s the way they are. Why is everyone is fixated on who loves whom…what the world needs now is more love, more fun, more kindness, more compassion, more empathy, more joy. https://yadadarcyyada.com/2015/07/03/how-to-be-good-to-one-another/ It has taken a long time and there are still haters (haters gonna hate) out there, but I bet many people are happy to see a light at the end of that rainbow.

I wonder when that day will come for people with chronic illnesses like Fibromyalgia, or people with mental health issues, or people with Autism, etc.  I wonder if or when people will see them, really see them, for who they really are:  your Mom, your child, your sister, your friend, your co-worker, your Dad, your teacher, your brother, your minister, your neighbour – just people.

Don’t judge people.

Have a little empathy.

Those people might be: interesting, fun, brilliant, a hope for the future, a good friend, or something more than a friend, someone to talk with, walk with, someone who inspires you, or but most of all, who gets you, but you’ll never know if you make judgements, make assumptions.

Don’t miss out!

Copyright D. Parker (aka Donna Parker/yadadarcyyada) 2013-2019. All opinions expressed are that of the author and do not necessarily reflect those of Fibromyalgia London Group (FLG).


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