Just Dabby

20/07/2024

Moments come and go but memories last forever..
Korea days with hon :)

18/07/2024

18/07/2024

17/07/2024

16/07/2024

Meet our newest furbaby... MOCHA!
Thanks Sis Nory & Bro Elf! ❤

15/07/2024

🙏

13/07/2024

🧏‍♀️

11/07/2024

Frappe with a breathtaking view and some quiet time... just what i needed today...

08/07/2024

🙏🙏🙏

04/07/2024

I'll have a side of beach with my coffee...

02/07/2024

You never know what someone is going through until you walk in their shoes. This is soooo true.. & iam thankful to meet some of my sclero sisters who are fighting this disease like me. We know & share the same pain & suffering...

To our fam & friends as well as my sclero group & their loveones, thank you for understanding & loving us. Even if our health is unstable & we may not be "normal" for others... as we struggle in fighting this disease everyday, you chose to stay, pray, care for us... ❤️ Thanks for making us feel that we are not alone in this journey...

28/06/2024

Yes to this!

ctto.

27/06/2024

Too bad i can't attend this event... how i wish next time, the venue is in Tagaytay or nearby... 🙏

Iam still thankful to those who organized this gathering to raise awareness that there is a rare autoimmune disease called Scleroderma, to let our family know what we're going through, how we live our lives with this condition and how it affects us, our mental health and how the society in general treats people like us...

Hope to meet my fellow sclerosisters next time...❤️

And thanks sis Weng for being consistently supportive to our sclero group!

24/06/2024

This.

22/06/2024

Morning coffee on the beach...

22/06/2024

June is Scleroderma Awareness month

20/06/2024

Miss going on dates with you...

06/06/2024

This is soooo true☹️

03/06/2024

✅️

01/06/2024

Some people think that to be strong is to never feel pain. In reality, the strongest people are the ones who feel it and accept it.
I've been fighting this disease for a long time now, probably have it since birth but it was diagnosed when i was in high school. Though i acted normal, when it flares up, i feel unbearable pain that i can't explain. There are days that i can't even get out of bed or feel tired for no reason. When i have the energy and happy mood-- that's good days!
Scleroderma is chronic, autoimmune disease, has no cure and lasts for your lifetime. Behind every warrior like me, there is an even stronger family who stands by us, supports us and fight with us.
I don't know if we will ever win this battle or how long this journey will take us but im still praying for cure and for people not to judge us because we are already suffering.

31/05/2024

To my fam & friends who always include me in their prayers.. THANK YOU! It really means so much to me to know that you care for me and think about my well being... ❤️

Iam praying that one day, i can tell my story of how i overcome what i went through and due to my resilience & prayer, it will be someone else's survival guide. 🙏

30/05/2024

🤷‍♀️

24/05/2024

COVID cases are again rising and still happening widely... Senior citizens, immunocompromised and children are still the most vulnerable.
Here are some tips to stay safe & healthy during Covid 19:
Always wear mask. Observe proper hygiene. Eat nutritious foods. Drink plenty of water. Take vitamins & supplements. Sanitize your home. Avoid exposure and take care of your mental health too.

Ingat po tayo sclero sisters...🙏

22/05/2024

❤️