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KLS
The following video is a short clip from the interview I had with Dr. Nathaniel Watson M.D., M.Sc in Seattle this past February. I am grateful to be able to speak out about Kleine-Levin Syndrome (KLS) and help those that are suffering. Thankfully, my KLS episodes have improved and are much lighter now! For a while, it was like taking 1 step forward 3 steps back every time a KLS episode hit. Now it’s like taking 3 steps forward, 1 step back when a KLS episode hits! It’s not what you go through that makes you the person you are, it’s how you react to the situation that you are dealt with that makes you the person you are. I have looked beyond my struggle and have found meaning in my life by helping others!
I am grateful for the blessings in my life, and I offer those interested the opportunity to bless someone else’s life by sending them a card in the mail on me. I enjoy helping others send a card to someone who needs to hear from them. I have spent the past six years dedicating my life to raising awareness for Kleine-Levin Syndrome (KLS) in an effort to help other sufferers by raising funds for research, engaging and connecting with the community, and facilitating the KLS Foundation website. Contact me here if you want to send a card to your loved one: http://alannawonglife.com/contact/
If you are struggling with KLS, I want you to know it does eventually get better with time.
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I hope you enjoyed this post! If you did enjoy it, please share it with your friends and leave a comment below! I love hearing from you!
All the best,
Alanna Wong
P.S. If you haven’t read the introductory section of my book about my 13 year battle with Kleine-Levin Syndrome, you can read it here: http://alannawonglife.com/real-life-sleeping-beauty/
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