DAY IN MY LIFE | Life before lockdown 2.0 !
HTML-код
- Опубликовано: 12 сен 2024
- PREVIOUS VIDEO: • Nephrotic Syndrome | I...
So lockdown 2 is upon us in the U.K. and for some like me it means back into some sort of hibernation from the world..
For those who may need the extra help mentally in the U.K. then 'Samaritans' can help
"Support is available from SHOUT, the 24/7 UK text service for people in crisis, on 85258. You can find out more about their service on the SHOUT website. giveusashout.o... "
Stay safe folks, Jasmine x
----------------------------------------------
⭐️ INSTAGRAM: www.instagram....
⭐️ TIKTOK: / _jasmine_shen_
⭐️ SUBSCRIBE: / jasmine%e2%80%99sjourney
⭐️ TWITTER: mobile.twitter...
⭐️ LINKTREE: linktr.ee/Jasm...
⭐️ PODCAST: go-be-more-pod...
⭐️ DONATE TO KIDNEY RESEARCH UK: www.justgiving...
My Favourites
💙 Water Bottle: amzn.to/30vE7hP
💙 Thermos Food Flask: amzn.to/3rw915q
💙 Yoga Mat: amzn.to/2N0afa2
💙 Travel Pillow: amzn.to/3t5tYEC
Disclaimer: Some of the above links are Amazon Affiliate links but cost you no extra - thanks for the support!
Disclaimer: I am not a doctor or in any profession of the sort. I am just here to share my experiences.
🤩 the castle looked gorgeous, good luck with lockdown 2.0
Isn’t it just?! Thank you- wishing you well!
ah you must be so glad you managed to make the most of the time before lockdown! I'm a shielder too, stay strong and stay safe!
Yes it was so lovely! Just tried to cram everything in before burring myself back in my flat! Hope you’re staying safe and sane!
Is nephrotic syndrome a lupus condition?
Hello, sorry I do not know the answer to this! However I’ve never heard of it being referred to lupus
You look ok, have you got swelling any where still
My swelling was all in my body, it had gone in my face by this point. I’m a petite person anyway so to look at me you wouldn’t see much swelling but I was definitely very swollen and struggling. I actually have a new video coming out soon all about my swelling in more detail :)
@@JasminesJourney i am 55 year old, year ago diagnosed nephrotic syndrome and minimal changes disease and had injections rituximab injection last year and dr said my antibodies normal no need moore injection, my albumen in blood was 13 and now 29, my urine not clear yet, I learn form your video, you share your experience..
Oh wow, can I ask how long have you had minimal change disease? Yes I have heard of the Rituximab. That’s good you don’t need anymore injections. I’m so happy you can take something from my videos!
@@JasminesJourney my legs swelled diagnoses April 2019.
Oh wow, well I wish you all the health and happiness in your journey my friend!