Love the message on these wheelchair gloves!
#wheelchair #wheelchair gloves #gloves #caudaequinasyndrome #ces #CESwarrior #ambulatorywheelchairuser #ambulatorywheelchairuser sexist #nevergiveup #inspiration #motivational
#CaudaEquinaSyndrome
#RaisingAwarenessForCES
#LearnTheSigns
#ChronicPain
#CesStrong #CesWarrior
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CES warriors!! Join us for our 2024 CES workshops across England. #CES #caudaequina #caudaequina syndrome #mycesstory #caudaequina championscharity #ihaveces #ceswarrior
People don't realize how exhausting it is to fight for your health every single day when you're in chronic pain. As you start this new week, remember that you are a warrior! πͺ
#CES #CEF #CES Warrior #CaudaEquinaSyndrome #CaudaEquinaFoundation #ChronicPain
π¦ Today is Rare Disease Day! π¦ Let's all share the day we joined the CES and rare disease community. When was your diagnosis and/or surgery?
#RareDiseaseDay #RareDiseaseDay 2021 #CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
You are stronger than you realize!
#CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
Ask the Expert Thursday at 6:30 PM EST followed by support group sessions with your fellow CES Warriors.
Get your tickets at Eventbrite, follow the link below.
Thank you to our donors for making this possible! π
Hope to see you there!
#CESuppot #CESExpert #CESLife #CESWarrior
Friendly reminder as you begin your week. You are strong and can tackle whatever is thrown at you this week! πͺ
#CES #CEF #CaudaEquinaSyndrome #CaudaEquinaFoundation #CES life #CES warrior
Some days even the tiniest tasks take a huge amount of effort when you're living with CES. Be kind to yourself.
#CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
Something to think about as we begin a new week. There are still a lot of great things in life hidden amongst the chronic pain.
#CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
Do you have a system in place? A sign on the fridge? A specific emoji you text? Let's hear how you make off days work in your family!
#CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
What is the best advice you have for parents who are new to CES? What about for those with CES who may be thinking of having or planning to have children in the future?
#CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
Have you found a way to explain your CES diagnosis or new physical limitations to the kids in your life? πΆ What have you found is the best way to describe it in words they understand? π§
#CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
As we head into Rare Disease Day 2021, let's talk about how you ended up in this community. Do you remember what your first warning sign was? What about your first red flag?
#RareDiseaseDay #RareDiseaseDay 2021 #CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
The treatment path and recovery plan can look very different between CES members. What therapy have you found the most helpful? Has it been a combination of multiple therapies?
#CaudaEquinaSyndrome #CaudaEquinaFoundation #CES #CES Warrior #CEF
We want the same things everyone else does, but we just have a few extra added challenges making it more difficult along the way.
#CES #CEF #CES Warrior #CaudaEquinaSyndrome #CaudaEquinaFoundation #ChronicPain
For those of us battling winter here are a few tips for surviving this cold weather!
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Is there anything you find helpful that you don't see on this list?
#CES #CEF #CES Warrior #CaudaEquinaSyndrome #CaudaEquinaFoundation #Winter
