Nobody tells you how strange it feels when your own body stops feeling trustworthy.
Before MS, I never thought about walking. About balance. About exhaustion. About whether my hands would cooperate today or whether my brain would suddenly feel like it’s full of wet cement.
Now I do.
Some days are normal enough that I almost forget.
Other days I sit in bed staring at the wall because my body feels unplugged from reality.
The weirdest part is that most people can’t see any of it.
You learn very quickly how to smile through fatigue severe enough to make your bones feel heavy. You learn how to say “I’m fine” while silently calculating whether you have enough energy left to shower.
This blog isn’t going to be inspiration porn.
I’m not here to pretend chronic illness made me a better person.
Sometimes it made me angry.
Sometimes bitter.
Sometimes terrified.
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Nail art warriors for Maria 🧡 • 🇫🇷 Ce post spécial est dédié à notre Nail Art Warrior aka Maria de @so_nailicious 🧡💙 Comme certaines d'entre vous le savent peut-être, Maria est atteinte de la SEP (sclérose en plaques) et la maladie lui a, entre autres, fait perdre sa capacité à réaliser de magnifiques manucures. Maria, avec cette collab, nous tenons à te dire de continuer à te battre telle la véritable guerrière que tu es ! • 🇬🇧 This special post is dedicated to our Nail Art Warrior aka Maria from @so_nailicious 🧡💙 As some of you may know, Maria has been diagnosed with MS (multiple sclerosis) and the disease took away her ability to paint beautiful nail art designs, among others. Maria, with this collab, we want to tell you to keep fighting like the warrior you are! • Thank you Magda @redheadnails for organizing this collaboration. All of our creations can be found under #nailartwarriorsforMaria 💪 • Girls involved in this collage: @aleksandras_bunte_welt @geolena_koski @gotnail @jemima.nails @lochnailsmonster @kathagraphie @nailistayco @marinelp91 @lacktraviata @mission_polishable @paulinaspassions @hefersanja @zephyronica @nailart.by.nici @bentesorberg @nailartfan95 @coffeeandnailpolish @mettedamgaardpedersen @rums2016 @dc_nailsart @katieabheda @barbouilleuse @crenailit @megans_manicures @ledanails82 • #ms #msawareness #mswarrior #mswarriors #spreadingorange #invisibledisease #endms #multiplesclerosis #thisisms #spreadingorange #msawareness #nailsforthecause #nailscommunity #nailart #stampingnailart https://www.instagram.com/p/CoK0k9Mtf6i/?igshid=NGJjMDIxMWI=
“Our ancestors have invented, we can at least innovate.” ― Amit Kalantri
DISCLAIMER! As a heads up, I want to let you know that I am still learning about my roots, my family, and my ancestors' stories. I am NOT an expert, but I will continue to do my research and share my findings with all of you.
For those who don't know, June is officially Filipino Heritage Month in Canada (and recently in Ontario)! It has brought so much joy and pride knowing that the Filipinx community is being recognized for their contributions from coast to coast.
As a Filipina-Canadian who was born and raised as an immigrant on a beautiful land called Turtle Island (settler-colonially known as North America) -- I do acknowledge that my family and I are guests in Canada and my roots are from the Philippines. Part of my roots is from Northern Philippines in a province known as Abra.
It turns out, I am a descendant of an Indigenous Mountainous Tribe called Tingguian (meaning People in the Mountains) due to my paternal-grandmother. My ancestors had tattoos on their bodies with beautiful meanings (including beauty and honour). They were able to hunt and fish for food and weave baskets and dye the fabrics for clothing.
1-2 years ago, I was able to order a dark poncho made by the Tingguians in Abra via Pinas Sadya (a local Filipino shop). When it arrived On the front, it had red threads sewn on the borders while there are four frogs from all four directions (N, S, E, & W) facing the star in the middle on both sides. Based on what I was told: "The weaves with frogs are typically worn during the rainy season. It is the belief of the tribe that it pleases the gods and will give them a bountiful harvest". From that point on, I knew that I would wear it in April each year for April showers (and May flowers lol).
Overall, I am happy and grateful that I am a descendant of the Tingguian tribe. This is a really cool fact that not a lot of people know about me. To be honest, I don't blame them. Every day is a new learning opportunity and I see it with a glass half full. I'm so happy that I found out how my ancestors were like prior to Spain's colonial invasion. However; I wish my grandmother was still here to tell me how much she knows. As the granddaughter of the Seeker of knowledge and wisdom, I am living up to her name by learning and asking questions of my ancestors' past and their way of life. When I have kids in the future, I will be sure to tell them about this part from my side. It is important to learn about the past in order to have a better future for all of humanity.
p.s. Please let me know if you or anyone knows where I can get more clothing made by the Tingguians. I would love to wear more clothing made by them ♥.
March is National MS Awareness month! I created these scrunchies to show my support! All proceeds will be donated to the National MS Society. Show your support here
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
✓ Live Streaming✓ Interactive Chat✓ Private Shows✓ HD Quality✓ Free Actions
Free to watch • No registration required • HD streaming
Yes it's pink, no it won't stay pink- but it's going to be a fun project to keep me busy for a while 😀 #mscansuckit #multiplesclerosis #mssociety #chronicillness #chronicpain #msawareness #mswarrior #spinergy #spoonie #wheelchairwarriors #wheelchairfitness #wheelchairproblems #wheelchair #wheelchairpro #cyclonewheelchair #passthetoolkit
Hi.
I’m someone living with Multiple Sclerosis, trying to navigate a body that occasionally treats itself like an enemy.
This blog is a collection of thoughts, symptoms, bad days, small victories, medical chaos, art, exhaustion, fear, dark humor and everything in between. Some posts will be raw, some angry, some strangely beautiful. That’s just what living with a chronic illness looks like sometimes.
“Living With Lesions” isn’t about pretending to stay positive all the time. It’s about being honest. About documenting what MS actually feels like: The brain fog, the fatigue, the uncertainty, the loneliness, but also the resilience people rarely talk about.
If you found this blog because you also live with MS or another chronic illness: Welcome.
You are not alone here.
And if you’re simply here to learn and understand : Thank you for listening.