THE PAIN OF LUPUS: FACING GRIEF HEAD-ON
Vložit
- čas přidán 23. 07. 2024
- THE PAIN OF LUPUS: FACING GRIEF HEAD-ON
#worldlupusday #lupusawareness #styledunderlupus
Thank you for subscribing! My name is Nathalie. I am a lupus warrior, and I love you! ✨💜✨
Let’s talk about lupus and coping with grief.
This space is about spreading lupus awareness. I also talk about the connection between trauma and chronic illness. I share some information I’ve learned from living with lupus. I was diagnosed with lupus in February 2020. I still have a lot to learn and would like to learn from you if you’ve had the illness much longer. I use this space to share resources and insights I've found helpful along the way. If you're looking for information regarding lupus awareness or encouragement after diagnosis, subscribe to my channel for weekly videos about mental health and chronic illness! I hope this space helps someone going through the same lupus journey. Thank you for watching!
“If you are unkind to yourself, you will be unkind to others. And if you are negligent of yourself, you will be that to others. Only by feeling compassion for yourself can you feel compassion for others. If you cannot love yourself, you cannot love others, and you cannot stand to see others loved. If you cannot treat your own self kindly, you will resent that treatment when you see it in anyone else. If you cannot love yourself, loving others becomes a harrowing endeavor with only occasional moments of comfort. In other words, loving others, or how you treat yourself, is your own dose of your own medicine that you really give to others at the same time.” Gary Zukav, The Seat of the Soul
Check out other videos:
Top 10 Inspiring Celebrities With Chronic Illnesses | Lupus: • Top 10 Inspiring ... Celebs Battling a Chronic Disease: • Top 10 Inspiring ... Inspiring Celebrities with Mental Illnesses: • Inspiring Celebri...
Shop my vintage and preloved designer accessories: www.styledunder.com/
Follow me on social: Linktr.ee/ntuitivehealing
For collaborations and business inquiries email: styledunder25@gmail.com
Resources: Lupus Foundation of America: www.lupus.org/resources
Free Online Therapy for Depression: cimhs.com/
24 hrs National Suicide Prevention Lifeline: 800-273-8255
Find a Lupus support group near you: www.lupus.org/resources/find-...
Lupus warrior Lupus Lupus symptoms Lupus rash Lupus CZcams Lupus treatment Lupus nephritis Lupus erythematosus Lupus erythematosus treatment Lupus disease Lupus anticoagulant Lupus erythematosus meaning Systemic lupus erythematosus SLE Systemic lupus erythematosus nursing Lupus symptoms for women Systemic lupus erythematosus symptoms Systemic lupus erythematosus signs and symptoms Lupus flare-up Lupus flare Lupus up triggers Lupus flare treatment Lupus flare triggers My lupus story Lupus story Lupus youtube Lupus treatment Lupus nephritis Lupus erythematosus Lupus erythematosus treatment Lupus disease Lupus anticoagulant Lupus erythematosus meaning Systemic lupus erythematosus Systemic lupus erythematosus nursing Lupus symptoms for women Systemic lupus erythematosus symptoms Systemic lupus erythematosus signs and symptoms Systemic lupus erythematosus signs and symptoms Lupus and depression Depression and lupus Lupus and depression Lupus and anxiety Lupus and depression treatment Lupus and manic depression Discoid lupus and depression Lupus and major depression Clinical depression and lupus Lupus brain and depression
This video is about the grief process involved with living with a chronic disease. In this case, I am talking specifically about grieving my Lupus diagnosis. What was that process like for you?
Cette vidéo porte sur le processus de deuil lié à la vie avec une maladie chronique. Dans ce cas, je parle spécifiquement du deuil associé avec mon diagnostic de lupus. Comment s'est passé ce processus de deuil pour vous?
So much has changed: mobility, energy, cognition. Sometimes I don’t recognize myself anymore. Hearing from other lupies and making friends is the best way to feel connected and supported . Thank you for making this video 💜
Thanks for sharing! And happy to share this space with you 💜💜
It took me two years for my grief since my SLE diagnosis, I was diagnosed at similar time with you, and you are so wise, thank you for sharing your wisdom..❤❤
You are too kind. Thank you for watching! We are in this together. 💜
I am glad I am not the only one who felt this way. It’s still hard for me to let go of that anger 😫
That's understandable. I think it's ok for it to come and go 💜
I am living the angry part.
That's normal...been there!
I feel you 100% I am in the process of waiting on my lab results, and have been in and out of the hospital for the past couple months and and lost my hair in huge patches a couple years ago but I keep getting told I'm fine I look healthy yet my body is in excruciating pain and i can't even eat certain foods without it making it worse it's like I have to be so cautious with literally everything, it's like a pain that affects everything and it's hard to describe it to anyone unless they ve gone through it, I went from powerlifting and CrossFit to trying to walk my dog and walk up the stairs is incredibly just exhausting, it's not fun
Sorry, you are going through this right now. Did you find out more since you posted this comment?
The stay busy is me bc I haven’t gotten a diagnosis but I am sure it is autoimmune I think I am already processing on the second stage but stage one is just my personality bc the world needs ignored sometimes for me
Yeah staying busy is a good way to avoid feelings lol especially the kind we are not ready to deal with
Meeeeeee never ready
@@Pearlisms I don't blame you...everything comes at the right time.