Welcome to Olivia's Personal Page
Do you ever wonder why I have been cooking food from scratch? I was diagnosed of Sjogren's three years ago.
Hello Friends and Family,
I’m so grateful for your support, especially during this very challenging time. I worry about my friends, family and associates, but I know we will all get through this together. I'm very hopeful that our crises are and will continue to get better each day. Even though we have been faced with this world-wide crisis, my heart to work on the fight against Sjögren’s can’t stop because Sjögren’s disease doesn't stop.
I was diagnosed of Sjogren’s on 17th September 2019 after a few episodes of parotid glands flares up and a lab order prescribed by my otolaryngologist back in July that year. Afterwards, my rheumatologist recommended me to participate in a patient conference by Sjogren’s Foundation in fall 2020. I have been passionate about this cause since. The foundation is dedicated to increase awareness, education and research for Sjogren’s, which is an autoimmune disease that affects the entire body.
Please join me in my efforts by making a donation today (on this fast and secure site) http://events.sjogrens.org/goto/Olivia_Luk. For friends and family with a non-US credit card, please Use this Link HERE.
-Gift Amount: Select amount to donate, such as: $100.00
-Select One-time Gift
-Would you like to make this a tribute gift? Must say/check off YES
Yes, dedicate my donation in honor or in memory of someone.
-Tribute Type: In honor of
-Honoree Name: Must say: NY Walk – Olivia Luk
Would you like to notify a friend or family member of this tribute? Please Email to Olivia6@gmail.com
-Your Message: Put in following Message: NY Walk - Olivia Luk
-Your Information – Fill Out your name & address
-Then Fill Out your Payment Information
Be sure that you send me the donation confirmation.
Also, it is very important that you select “Tribute Gift” and note that it is for New York Walk – Olivia Luk
What impact will your donation make? To name a few, 1) It provides valuable patient support and Sjogren’s foundation; 2) There is no cure for Sjogren’s at the moment. However, the foundation has continued to make great progress in encouraging research finding new therapeutics for Sjogren’s; and 3) it serves as the voice of all Sjogren’s patients especially in the times of COVID-19. (Please no pressure if you aren't able to help during this challenging time. I appreciate your consideration.).
If you want to learn more about the foundation, here is the Sjögren’s Foundation website www.sjogrens.org
Also, if you can make it, please join me on the Zoom Virtual Opening Ceremonies at 10am ET this Saturday, 22nd October. I would love to see you on the call. Then afterwards, we can all walk from wherever we are safely! Let me know if you can make it and register here 2022 New York State Virtual Walk for Sjögren's - Walk for Sjögren's!
Together we will make a difference towards conquering Sjögren's!
Stay safe and healthy first and foremost.
(PS, if you would rather send a check, please send it to the Sjögren's Foundation (10701 Parkridge Blvd, Ste. 170, Reston, VA 20191), noting my name and New York State Walk on the check)
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