LIVING WITH LUPUS | MY LUPUS STORY | 3 Months & My Life Has Changed | Lupus Awareness Month 2020

Описание к видео LIVING WITH LUPUS | MY LUPUS STORY | 3 Months & My Life Has Changed | Lupus Awareness Month 2020

LIVING WITH LUPUS - THIS IS MY STORY - PLEASE WATCH TO THE END - Lupus has changed my life; from Jet setting, jumping out of planes and featuring on UK hit show SAS WHO DARES WINS. I now find myself struggling to walk down stairs most days. I'm 3 months into my diagnosis and this is what I have to share with you. I hope you find it useful and informative it took a lot for me to go this deep.

DON'T FORGET TO LIKE👍👍👍👍👍👍, COMMENT And SUBSCRIBE

Drop a purple heart in the comments section so I know you are real :)

|| Questions ||
1. Improvements since diagnosis?
2. Do I keep fit?
3. How am I coping?
4. Has my diet changed?
5. Do I take pain relief?
6. Do I feel confident?
7. Do I have any habits/rituals?
8. Do I set goals?

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|| LUPUS AWARENESS MONTH ||
Lupus UK: https://www.lupusuk.org.uk/lupus-awar...
Lupus Foundation of America : https://www.lupus.org/lupus-awareness...


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♡CHECK OUT MY OTHER VIDEOS♡:

MY FIRST EVER VIDEO My Story Living with Chronic illness :    • MY LUPUS STORY | LIVING WITH LUPUS | ...  

Top Tips | Living with Lupus | Chronic illness:
   • Видео  


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✩ s o c i a l s ✩
I n s t a g r a m ↠ @sybella.davis

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LAPACHO TEA ➥ https://amzn.to/2SrVA7g

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☆ ---- MY FILMING SETUP EQUIPMENT ---- ☆

● Laptop - Apple Macbook pro 13 inch ➥ https://amzn.to/2X7avVJ
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*DISCLAIMER: This video and description may contain some affiliate links, which means that I may receive a small commission if you click on some of the product links and decide to make a purchase. however, items included in this content have been purchased by me, and my opinions and recommendations are 100% honest.
Thank you for supporting Simply Sybella so I can continue to provide you with free content each week!
xoxo


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In this video I share my story living with Lupus SLE in my life, how it's changed me and my life since my recent diagnosis. This auto immune disease is no joke, Chronic illness's are no joke. I never knew I could experience chronic pain and extreme fatigue like this. Lupus awareness month is a time for me (us) to learn more and connect with this community, raise money as well as awareness.


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☆ ---- Connect with me ---- ☆

☆彡My Email ► For Business Enquiries please contact: [email protected]



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Welcome! This channel is a space for anyone interested in TIPS 'N' TRICKS, and delving into my lifestyle.
Learn how to tame your natural curls and what it's like to be a young, active, brown girl in the UK living with Lupus SLE.

It's time to uplift yourself, your curls and others - let's go!




|| Thanks so much for watching ||

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