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Wtf does this have to do with lupus terrifying psychosis

How you doing now days ??

I was so lucky 😍 to get cured permanently from HIGH RISK HPV by DR ALAHO OLU on TH-cam Channel………..

How you doing now days ?

Newly diagnosed here. I really enjoyed your videos, I couldn’t find you on Instagram. I hope you are doing well.

What an amazing mother!!! ❤

the struggle is real! thank you for sharing part of your story. I was diagnosed in 2007. it had been under control for a lot of years just with plaquenil and took some other medications intermittently - but my system went haywire in the summer of 2021. Ive been flaring hard ever since. I really appreciate hearing other peoples experiences. Blessings💫

Hello , how you doing now days ?

Amen! Praise the Lord. By His stripes, we have been healed. All disease is from the evil one, and Christ overcame the disease devil on the Cross

How you doing now days??? , I hope you doing great

Accepting the things you cant change. And changing the things you cant accept. ❤

Ur mom is the best❤❤❤❤❤

God has given you special gifts! Your personality, you can hold our attention….your beautiful, quick witted, and a beautiful, blessed soul! You shine bright as the sun! Now you know with all of this energy, God is seasoning you for His purpose! I cannot wait to see what you do with your precious life! I know you will Rock!!❤❤❤

I was told I had Lupus in 2010. I didn’t believe it as I never had the malar rash which I thought was the standard symptom. and previously in 2008 at Mayo Clinic I was told I had Sjogrens syndrome. I’ve had lots of different symptoms over the years but I never stop to think that it could be autoimmune related because I don’t know enough about it. I just wonder what is going on and why I feel the way I do. I’ve been in and out of the dermatologist lately with rashes on my right shin they say is dermatitis /eczema the skin biopsy was negative for lupus. I was told follow up with Rheumatologist but after 6 Rheumatologist since 2008 I decided on just going to my primary. He ran tests in November 2023 and said looks like you probably have Lupus. I never told him of the diagnosis in 2010. I can relate to a lot of the symptoms you describe and I sleep in my lazy boy recliner every night as it’s in my room. I’m still doubting my diagnosis and tell myself when I don’t feel well that it’s because of something else. I’m supposed to find yet another Rheumatologist to go to but the last one literally told me I was a puzzle so I got discouraged and stopped thinking about it and never went back. One Rheumatologist in 2010 did put me on Plaquenil but later said nothing was wrong with me. Here we are in 2023 and a new doctor telling me I believe you have Lupus and tells me to go to a Rheumatologist. I’m frustrated and afraid to go that’s why I been researching online lately. I just don’t understand if some of my symptoms could be lupus related or normal things everyone gets on occasion. Thanks for sharing your experience here with everyone….

💜🙏🏾💜😇

The platelets make your blood clot ! For instance, I have a clotting disorder where I get dangerous un neaded blood clots so I am on blood thinners whereas you, you cannot produce clotting when youneed it

How are you doing today

Hey! How are you feeling now?

I am Amie Batchelor, and I work for MediTalk, part of Medicys, an international healthcare research company. We are currently conducting research on Lupus (CLE) in the US with Clinical Outcomes Solutions. Participants must: • Be 18 years of age or older • Have a clinical diagnosis of active Cutaneous Lupus Erythematosus(CLE) • Able and willing to take part in an in-person study taking place on two consecutive Saturdays in Boston (29th July, and 5th August) Compensation: • 300USD for Weekend 1 ratings (29th July) + 300USD for Weekend 2 ratings (5th August) + 100USD for an optional extra 1-hour interview. Total Incentive: Up to 700USD. Accommodation and travel costs can be covered within budget. Foods and drinks are included. This research is confidential. Any contact information you provide will only be used for the purposes of compensation and interview scheduling. We also offer an extra referral fee: 100USD to you for anyone that you recommend who completes the study. If you are interested in participating, Please contact us at a.batchelor@meditalk.world or by phone at +44 1765 502 355. We are accepting participants until Friday (14th July 2023) this week only. Many thanks

Jasmine, How are you doing in your lupus journey… please update your journey

Yeah she say she sleep in the bed and all she hears banging at the door she get up in this is all that matters I'll let you know the type of s*** is that true story

Okay the mama say when they got there they found her on the floor with a okay now listen to the daughter

You are beautiful and blessed 🙌

Thank you so much love ya!

The shin pain and swelling is not talked about enough. I’m having a flare now, pray for me 😩

God is a healer. You are a survivor and inspiring to be so young and go through this. Bless you love

Jazmine, Are you making anymore videos ? I was wondering how you are doing ?

Reach out to Dr Isibor on TH-cam, cured me from Lupus with his Alternative Herbal Healing in less than 3 weeks #Drisibor

I know exactly what you going through, Reach out to Dr Isibor on TH-cam, cured me from Lupus with his Alternative Herbal Healing in less than 3 weeks #Drisibor

Wow!! Praise God!! I am so sorry what your go through. I’ll have your on my prayer list. You both are so beautiful and love your heart for the lord. I feel the same way in spirit. God bless you

I have lupus also, it is so interesting the different symptoms we have. I used to break out in hives and the itching drove me nuts, but at the time I didn’t know I was sick. You tell your story so we’ll I wish you would make more videos. Peace and ❤️

I was about to give up because the pains are too much...and I found your channel.

🖤

I don't get why it can be so much worse on few than others, it's so cruel. My heart aches for you as I only have chest flares every so often but never as bad as you describe. I can't imagine how strong you are as an individual 😭💔

Damn, you're a REALLY cool person. I love your attitude. I've been finding it difficult to keep a brave face during my flares. I work in aged care, so being close to elderly patients most of who are experiencing such a significant amount of both physical and emotional pain yet are still able to keep a smile on their face is that one reminder that keeps me going through my shifts and stops me from feeling so bad for myself. Thanks for making these videos and spreading awareness. It really inspires me. ❤️

Thanks for sharing your experiences. I’m new to the lupus world & have been learning so much from your videos, stuff that my doctor would never be able to prep me for 💜

Girl u did your research

Thanks for this. I got my diagnosis for Auto Immune Disease. So i am doing some research. Thanks for this video. They i am waiting on the results back from my labs which include Lupus.

it was a girl on youtube who died of lupus but can’t find her page

Thank you for doing this, I’m also a young blank woman (19) and my doctors are starting my blood work for lupus/rhemu. arthritis

Hello Ms Jazmine Wise. I am a first time viewer to your channel and l want to say thank you so, so ,so much for your video. You are so Beautiful inside out. I have been diagnosed with Lupus since 2019. I have never heard of lupus. My mine, and body is all over the place. So many difference kind of flare up. I am trying g to be strong through it all. Everything that l eat mess my stomach up. Joint pain in my wrist can open bottles and drop everything. My back flares up all the time where l have to go to the ER. You are truely an inspiration to us all. Continue to be strong make more video and hold on to God's unchanging hands. God bless your mom, your little sister and your Family. A support system is so well needed. I have subscribed to your video. So helpful. You are well educated and thank you for sharing. God bless you my Beautiful Sister.

I was just diagnosed with lupus a few days ago I was dealing with flares for awhile but never knew what it was till a few days ago my doctor was very confused what was wrong with me and made me get a bunch of lab work done and now that I know what’s going on I’ve been scared and I had no idea what lupus was and I’m still learning about it . It’s scary honestly but I have hope I will live a long life

God is a healer

Really appreciate your mom's energy when it comes to belief & research! It gives me motivation to pursue my treatment more rigorously. Thank you both! May you never experience a flare like this again ever🙏🏽

Most Blessed testimony....Blessings of continued healing to you young lady.

God bless u thanks for sharing

Motrin does nothing for me I usually end up in ER

Methotrexate is ok. Prednisone causes major flare up for me

The knee swelling sucks n the fatigue.

My blood work had high RA levels weird