Carol Foote

Wife, Mother,
I suffer from CRPS and fibromyalgia - chronic pain.
I am a hockey fan - Maple Leafs, Marlies

[Princess, The Tower @APainPrincess]

“I have pain 24/7…severe #nervepain. It’s in all my limbs, spine, neck, face… I miss myself—I want to be free of pain and live again… How can anyone understand this? Tears fall from my eyes…silent tears…slowly grieving my lost life.” https://t.co/jB9b8Ik3lX #NERVEmber

[Carol Foote @recdfoote]

@Leafslatest ..

[Carol Foote @recdfoote]

@APainPrincess Me too!!

[Carol Foote @recdfoote]

@thehazelmae My son works for the Jays Accessible team. Never a harder working crew you will find

[Carol Foote @recdfoote]

@WriteEditPJ West Wing and Friends

[Carol Foote @recdfoote]

@thehazelmae @ShiDavidi My son works as an Accessible Support Usher at the Rogers Centre. They are also unsung heroes.

[Carol Foote @recdfoote]

@KnitAndCrit @PWHL_Toronto Our time slot was Thursday at 11. We just got an email to say sold out. We can try for half season tickets when they are released.

[Carol Foote @recdfoote]

@Sportsnet @KKiermaier39 Class act. He will be missed.

[Carol Foote @recdfoote]

@CalltoActivism Yes and I'm from Canada 🇨🇦

[Carol Foote @recdfoote]

@TeamCanada Whitby Ontario

[Carol Foote @recdfoote]

@TheBabalicious I feel your pain. I was at a concert last night. I had a great time. Today my body is paying for a fun night out. Sore back, swollen feet, sore legs. Heating pad is my friend. I am also sipping on a cup of nice warm tea.

[Carol Foote @recdfoote]

@TheBabalicious I had it two nights ago during a rare date night with my husband. I could wait to get home to get my heating pad on it and to take a CBD pill

[Carol Foote @recdfoote]

But some days are so painful.

[Kara @TheBabalicious]

Dear Fibromyalgia, .... No-one said it would be easy........

[Carol Foote @recdfoote]

@keithedwards Follow @ddale8 he is fact checking live and will be on @CNN after the debate.

[Princess, The Tower @APainPrincess]

“I miss feeling productive. I miss feeling spontaneous…I miss not being exhausted constantly. I miss feeling like I had a future… I’m trying hard to find my identity again. I have lost so much…after I worked so hard to become who I was.” https://t.co/5W1vzK76ed #chronicillness

[Carol Foote @recdfoote]

This is me. Some days are so hard.

[Princess, The Tower @APainPrincess]

“I can walk, but I can’t walk very far, and it’s always with #pain and #fatigue. I can stand, just not for very long. Limited as my mobility is, I’m still made to feel like a faker. I don’t look sick enough. I don’t look #disabled enough. I’m too young.” https://t.co/IiFdGCpOWD

[Kara @TheBabalicious]

Dear Fibromyalgia,

[Carol Foote @recdfoote]

@iafflocal465 @OshawaFire @oshawacity @IAFFCanada @IAFFofficial @opffa @WPFFAL2036 @claringtonfire Gordie will be missed.

[Carol Foote @recdfoote]

@bend_ro @RossKneeDeep No thank you. Canada does want them

[Princess, The Tower @APainPrincess]

“I feel isolated all the time so when someone reaches out to me just to catch up, check in, or say hi, it can quite literally make my day. Text me, message me… anything to remind me that you’re thinking of me and I’m not forgotten.” https://t.co/iJo99LVqwN #chronicillness