Відео

How have you been doing? Any updates? I was just diagnosed with AS and I'm inspired by your dancing videos!

Sorry I couldn’t make it!

Thank you for finally posting!!!!!!!!!!

Thank you for sharing. I have been struggling to get a diagnosis for 5 years. The pain and discomfort have taken a toll on me. AS is difficult to pin point. I was told AS is what I have.

Wow two studios at the same dance Competition

How long did you have to stay there?

Jillian I am in your leaps and turns class every Thursday and we all agreed that cosmic brownies are better!!!!!!!!!!!

That was so funny how Jillian said headlight instead of head level

You did a very nice job jillian! YOU HAVE TO VLOG MORE!!!!!!

The alligator you saw on the boat and you said you would name it purl. I would name it Timmy

anyone on xeljanz for it instead of humira?

Get the book: "No Grain, No Pain" by Dr. Peter Osborne. Game changer! Best of health to all.

Thanks for sharing you story. I was diagnosed in 2019 but for a long time my pain was dismissed and the numerous specialists did not seem to believe me. The rheumatologist finally took about 1/2 a year to diagnose me but I deteriorated so fast that I ended up needing a care giver and in a wheelchair. The Humira worked wonders but I suffered damage that could not be undone but I am better than my worst condition. I am military veteran but when I spoke of my symptoms, pre-diagnosis, the doctor basically called me a “wimp” with low pain tolerance. In reality, the pain was so severe that I wanted to the euthanized.

Thank you for sharing your story, I am dating a wonderful woman who was diagnosed with AS a few years ago and before meeting her I didn’t even know what this disease was, but hearing your story help me so much to understand the gravity of the situation. I hope we can find the HUMERA medication accessible to her. Thank you for sharing 😊😊😊

Stand strong you all. ❤

In the South, most Blacks are ~25% Europeans. The doctors don’t consider AS due to our phenotype (outside appearance) when they are supposed to have at least a little knowledge of the genetics of the populations they serve. Here, if you aren’t brave enough to stand up to the doctors who look down on you and TELL them what to test, by the time they find out you have AS, you bones are already fused and destroyed. They don’t even know how to read X-rays down here. I had to show the doctor my X-rays on my cell phone with the fusions circled. 😂 My sister is afraid to ask her doctors directly. She said they try to send her to Psych. She in a Police Captain (who mainly investigates Sex Crimes). She is way more stable in the mind than them yet they look down on her and provide substandard care. This is just for your viewers to see. I’m not in any way holding this against you. DO NOT listen to phenotypes (looks) comments from the doctor. It only takes one generation to change a family from white looking to black, to Hispanic, to Asian, etc. it’s also been proved there is 50/50 penetrance between males and females. Only about 2-5% have the genetic marker. FYI.

ua-cam.com/video/CV9KHSxvAAk/v-deo.htmlsi=V0JLt2aLoFPAzWsT

Humera is an immune suppressant, look that up. You need your immune system to stop cancers and a whole host of other stuff. My daughter has been diagnosed with AS and being a researcher in natural health, which is a hobby, I like to find out things that ‘they’ don’t want us to know, I have found the natural cure for AS. I will post this in a separate video, watch it to the end. Good luck guys. Here you go: ua-cam.com/video/CV9KHSxvAAk/v-deo.htmlsi=V0JLt2aLoFPAzWsT

Mmmm, tasty.

Nice dance performance

I’m a former competitive dancer (now medical school professor) and third generation AS sufferer. It’s a tough world for people with this condition. Sending love.

I got diagnosed a week ago, as per my xrays, they show the actual bone spurs waiting for the hlb27 gene results but it's better as i thought i was going mad. People do not care to understand what we go through, absolute torment. I will tell my doctor about the injection.

I wanna do dance so bad but im not sure if i can plus ill fell wierd i feel like i would be in a class full of small kids and be the only hs freshman in there...

I don't believe you kid, until you show how are you WALKING. Picture is worth 1000 of words. 20 minutes of yucking is just to make views for your channel.

You doing lots of harm to people who are suffering of AS. Instead of sitting and yucking, demonstrate how are you WALKING.

40 years of Ankylosing spondylitis, and trust me, I've tried everything, but the Carnivore diet is the only thing that works. Good luck.

LOVE THE MOOSE BACKPACK!!!!!

I think Sydney won the eyeball contest.👁️

So Jillian is my dance teacher and I am really grateful that she is my dance teacher.

Very very similar presentation and background to my story. Down to how I kept thinking I “just have to do more PT”. I feel your pain! Genuinely

Love this thanks for tapping!

Hello sweetie... What kind of injections are you on now? Cosyntex or something else?

Love this! I think the movement will help your AS!

I went dancing around Christmas… woke up in sooo much SI pain that lasted a week. Went dancing again New Years and I was fine. Go figure … with my AS I never know what to do or avoid because it changes so I think enjoying life and not limiting myself is what I do now.

Why is the maximum quality 480p...

I am also a AS warrior among other things. Just came across your video and wondering if you have made anymore about AS?

Very inspiring dance, even with as u are doing such a wonderful dance. I was quite emotional watching. Keep it up maam

Promo>SM

Was your diagnosed after the covid pandemic started? Did you happen to get the covid vaccine? I heard than alot of people who got the vaccine are getting autoimmune disease Currently in the process of being diagnosed Never had problems all my life But ever since i was forced to take the covid vaccine Back in February 2023 I suffer from so many different symptoms

Great job Miss Jillian

Hello. Sorry fot asking this but how is going with your as, are you still taking humira?

Keep moving and stay as flexible as possible. I have lost rounghly 89% of the lordotic curve of my lumbar spine from this.

I am glad they actually use the Antigen marker HLA-b27 to determine if you have it. WhenI was going through the mental games of being diagnosed it. They told me having a + result only ruled in the realm of possibility rather than a diagnosis of AS. I faced terrible games trying to get a diagnosis nearer 30 years ago. Thanks for your story, I hope those treatments work for you.

Are you completely recover from your Arthritis disease

thank you for posting this video, ive been having so much lower back pain & lumbar pain since last april, have barely slept for 2 weeks, and my grandma has this disease. Just got tested for the HLA-27 & it was positive. Still not sure if I have it but hearing your story literally made me feel so much better & not alone if I end up having it.

Ярко! Музыкально! Танцевально! Впечатляюще!!!!! Но!...Костюм немного напрягает.... Боди низкие укорачивают прекрасные фактурные ноги?! Зачем!? Мода!? Не стоит!!!

Can we be friends.??

Exquisite story telling!

She killed that and she's gorgeous.

Hi from Australia 😊 I'm a 57yr old woman, just been diagnosed with AS, a MRI shows i have "active disease" in my sacroiliac joints. I had already started Humira about a month ago for RA. I am positive for the hla-b27 gene. Thankfully here Humira is only $30 a month (2 injectables). I'm also on plaquinil, Sulfasalizine and meloxicam. Im lucky to have a great rheumotologist. All the best to you.