@kayandtayofficial: Now starts the next chapter of helping her to feel better! ❤️ backstory ::: I’ll do my best to summarize what’s going on for those who haven’t followed this health journey. For the last 5-6 years, Kay has suffered with a range of issues; fatigue, fevers, rashes, stiffness, and body aches, to name a few. When these issues got worse and worse, she started going to doctors to figure out what was wrong. Her doctors always gave different answers and would put her on medications that were horrible for her, and wouldn’t work. She never got a straight answer, and was always standing up for herself and recording all of her symptoms, to show the doctors that they might be wrong. There was always just guesses by the doctors and never a straight diagnosis, and so she started to do more research and understand her lab work. She started to notice that she had many of the issues from one illness, but when she would bring it up to doctors, they’d always say that it may be that but maybe not, and they would always chase different illnesses. Finally, about 6 months ago, kay went off of all of her medicine. She knew that the medicine that she had been trying was messing up the lab work that was being taken. So she hurt for months and months while trying to take no medicine so that her labs would hopefully tell her what was wrong. She had the test done, and it finally showed things that it had never shown before. She took it to her doctor, and her doctor finally decided that Kay was right all along. Now she is starting a new medication that specifically treats the illness that Kay has. And we will see if she finally feels relief after all of these years! It sucks that Kay has this illness, but now we can use the proper medication to help her to live a more normal life! ❤️ #kayandtayofficial #couples #relationships #pregnant #postpartum
✨Kay and Tay✨
Region: US
Wednesday 08 January 2025 20:59:18 GMT
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Jerri :
oh hunny!! that's a BIG diagnosis. I'm so glad they found this out now. I'm so sorry about the diagnosis and I'm praying for you
2025-01-08 21:19:47
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Leash :
Don’t ever feel bad about being excited or relieved for a diagnosis when you’re chronically ill and time after time people say there is nothing wrong but you know there is you’d rather know what you
2025-01-08 22:40:01
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HouseOfExile :
Healthy people will never understand the joy and relief we feel finally getting that positive test result after YEARS of suffering and every doctor being like “your test result are fine, nothing I can do” so happy you got answers
2025-07-24 10:39:38
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KJ :
So happy for you to have finally gotten answers!!! ❤️
2025-01-08 21:00:42
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Lissa :
my mother had systemic lupus i’m sorry
2025-01-08 22:19:14
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Sarah H :
I have a chronic illness and this battle is such a hard fight. congratulations
2025-01-08 21:03:19
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Jas :
I have that too! make sure you get a kidney biopsy to make sure the lupus hasn’t affected your kidneys since you’ve been undiagnosed for so long that’s what happened to me
2025-01-08 23:40:55
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LittleRed90! :
I have SLE lupus!! Welcome to the 🦋 Warriors Club
2025-01-09 00:31:02
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Heather 🇨🇦 Sjögren’s + Endo :
And if you have any questions about Sjogren’s or just need a fellow Sjogren’s friend, I would be happy to connect. ❤️
2025-01-09 02:44:34
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thea🎧 :
THE WAY ELLIE SAID “hayo >.<“ IN THE BACKGROUND 🥹
2025-01-08 21:02:01
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Kary Perales :
I also have lupus and it's normal to feel exhausted all the time
2025-01-08 23:10:25
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Marisol Ibanez :
I have sjogren's syndrome and SLE as well!
2025-01-08 22:36:01
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Caitlin Ann Farewell :
I’m so happy you have your diagnosis!!! 💕
2025-01-08 21:03:36
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The Queen of Weird :
Yay!! I, too, have SLE and Sjogrens! Along with fibromyalgia and hashimotos! There are support groups!
2025-01-08 21:06:58
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Abby🫶🤍🎀 :
what does fatigue mean
2025-01-13 02:17:57
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Elizabeth Maryana 🌸 :
I also have sjogren syndrome and also fibromyalgia.. I don't have a good life I suffer a lot actually I was thinking Kay has the same. I'm happy she can now find good medicines.
2025-01-08 21:05:51
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pheebs :
were you told there was nothing wrong the first few appointments with your dr? I have such intense pains in my body for no reason and my doctor said there’s nothing wrong due to blood results
2025-01-09 03:36:27
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Aly Yates :
When I got my diagnosis for systemic lupus and fibromyalgia I cried with joy. People were like “why are you happy? That’s horrible” no, I’m happy because I finally have an answer
2025-01-09 05:56:26
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Carrie Styers :
welcome to the autoimmune disease club! we are all here for you!
2025-01-10 02:58:24
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ℰ :
I’m so glad you have the answers after so long!!❤️
2025-01-08 21:04:10
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Renee🪩🎱🤍 :
Can I get an hey I love you’re video’s
2025-01-08 21:02:53
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Jordan :
I’m so proud of you for continuing to fight for answers! I have gastroparesis, intestinal dysmotility, and POTS, and the fight for answers is EXHAUSTING. It is a bittersweet moment, but you have the
2025-01-23 14:42:43
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Papillon_cœur🦋🥰❤️ :
I just diagnosed with fibromyalgia the symptoms sound very similar. all the best for you
2025-01-09 00:31:32
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Rachel :
I have a very serious genetic condition (Marfan syndrome). It’s SO important to always have someone at your appts with u. Another person to hear everything, ask ?s, etc is crucial, esp at specialists.
2025-01-09 06:30:18
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Catlin Michelle Gallant🦋 :
I have recently been diagnosed with sjogrens syndrome, yes some days are hard other days are better❤️
2025-01-09 02:08:39
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