#UCTD
A great Dec Fri in the Osler Medical Residency—a Firm of Choice Image of Osler with #stephaniealden on empyema, ACS rounds discussion of SLE nephritis with kidney 👸🏻ACS #christinatamargoand a Stevens Osler Grand Rounds on UCTD with #scottyeudall and Stevens ACS #benjohnson #oslerpride
December 19, 2025 at 7:01 PM
For me they just kinda stopped at Undifferentiated Connective Tissue Disease (UCTD) and like. I'd prefer it be differentiated, please. Had a rheumatologist tell me "if it's eds there's nothing i can do" okay? But *I* can do something if i know what it is. Like access a community.
December 17, 2025 at 11:11 PM
my rheumatologist when he diagnosed me with uctd:
November 9, 2025 at 3:03 PM
Kasha Monique
www.youtube.com
November 4, 2025 at 8:30 PM
UCTD is insanely prevalent in CrossWorlds lobbies, so now more than ever you should learn how to properly counter this build. Learn prime hot-spots on each track to target UCTD players with global items, and pay close attention to invuln downtime to prevent stuff like this!
October 30, 2025 at 7:07 PM
There are pros and cons to both UCTD and Item Management builds, and in some cases I think IM builds still hold strong. However, the sheer versatility you get from UCTD makes it a much more appealing option for me at least. It's kind of crazy that this build just does everything.
October 30, 2025 at 7:07 PM
I've recently adapted a hybrid UCTD-bagging playstyle into my matches, to great success.

I'm inclined to say that UCTD is WAY more toxic for bagging than actual item gadget builds. If your mechanics are good enough you can get away with insane smuggles completely protected.
October 30, 2025 at 7:05 PM
I’ve been on midodrine and modafinil together for a week now for what my neuro suspects is dysautonomia, and I’m cautiously optimistic. I’m experiencing less crashes and my blood pressure is stabilized. It’s crazy how many drugs I need to animate my corpse, but I’ll take it.

#Lupus #UCTD #HealthSky
October 12, 2025 at 11:21 PM
8pm today on my YouTube page, I have 2 new blends dropping. Then at midnight, I have 2 more coming out. I will try to add more. I'm trying to make more mixes & share them with you guys. I hope you listen & enjoy them as much as I do. Link below. ❤️

www.youtube.com/channel/UCtd...
Kasha Monique
www.youtube.com
October 3, 2025 at 7:37 PM
apenas uma parte pequena da lista de possíveis causas de fatiga

como é possível que possa ir de pressão baixa pra CÂNCER assim do nada

e uma parte boa das causas nem tem exame que pode atestar com certeza se a pessoa tem ou não

pqp vou me matar hoje mesmo
September 13, 2025 at 2:25 PM
That real boom bap

youtube.com/watch?v=uctD...
Kibunja Naino (Not In The Mood)
YouTube video by Hikaru Utada - Topic
youtube.com
September 4, 2025 at 11:14 AM
Those of us with #SmallFiberNeuropathy | #SFN | #Dysautonomia | #POTS | #Lupus | #UCTD

How do you get your water in?
Now that neurologist says I have to drink 32 oz of water every two hours, I really hate drinking water.

The worst part is, before RX, I suspected that I needed to drink that much. When I do manage to drink as much as she says, I have way less symptoms.

So I know I need to. But ugh.
a man wearing sunglasses says " absolutely not " no way
ALT: a man wearing sunglasses says " absolutely not " no way
media.tenor.com
September 3, 2025 at 12:52 AM
Really annoying that just as summer’s ending, my joints and nerves are more functional and in less pain, just in time for it to get cold and my winter flare to start all over again 🙃

#Lupus #HealthSky #Spoonie #UCTD #SmallFiberNeuropathy #Dysautonomia #Arthritis
a woman standing next to a couch with the words where 's my heating pad written on it
ALT: a woman standing next to a couch with the words where 's my heating pad written on it
media.tenor.com
August 31, 2025 at 12:21 AM
Absolutely insane that it’s 90 out and I’m wrapped in heating pads inside.
#Lupus #UCTD #Spoonie
August 12, 2025 at 5:04 PM
I went for a walk today! Just a short one, and I came back with a headache from the sun and crashed, but I got that D 😈🙌🏼
#Lupus #HealthSky #UCTD #SmallFiberNeuropathy #Dysautonomia
August 9, 2025 at 6:05 PM
I'm still getting my neuro workup. My neurologist thought from the jump that we're looking at small fiber neuropathy and dysautonomia caused by my UCTD lupus, and tests so far line up with her suspicion. The final test I need to confirm it is a table tilt.
July 30, 2025 at 8:46 PM
Characterizing circulating microparticles (MPs) in both symp. & asymp. ANA+ individuals revealed similarly elevated # of MP immune complexes, but with IgGs significantly less pro-inflammatory, suggesting instead differences in altered IgG sialylation

Arthritis & Rheumatology
doi.org/10.1002/art....
July 25, 2025 at 8:32 PM
Forgot to report back, but I'm loving my shower chair! I took my first everything shower in forever and it was glorious.

#Spoonie #HealthSky #Lupus #UCTD #Dysautonomia
It fits!! I sits!!

I'm already excited for shower time, which says a lot, considering it's usually my most daunting task.

#FuckLupus #SmallFiberNeuropathy #Dysautonomia #Spoonie #HealthSky
July 13, 2025 at 6:39 PM
I used to love summer - I worked at a camp, I went hiking with my dogs, I spent afternoons in my parents’ pool. But now if I spend time outside between 10am and 5pm, I need a full day of rest afterwards. It’s so frustrating being sick and it’s not something that’s just going to go away. #uctd #lupus
July 8, 2025 at 3:26 PM
Had the audacity to spend time with my friends and family in the sun this weekend and now I’m flaring. Just when I was starting to feel a bit better too 😞 #uctd #lupus
July 8, 2025 at 2:40 PM
Really? I often don't try with ER docs anymore. The EDS scares them enough that I don't want to explain how UCTD is not MCTD.
July 3, 2025 at 6:53 PM
oddly I’ve not had that happen (yet 🥴), but I have had to explain what UCTD is to literally every non-rheumatologist I’ve ever seen 🥲
July 3, 2025 at 6:48 PM
I’ve never come across someone else with UCTD before seeing this post 🥲 (and yeah it’s never an available option in systems 🫠)
July 3, 2025 at 6:29 PM
But the symptoms of UCTD vs. Ehlers-Danlos Syndrome, which is also a connective tissue disease, are different. We've currently got my UCTD under control via my immunosuppressants. My EDS.... *laughs until laughter turns to crying in the corner humming Smiths' songs*
July 3, 2025 at 6:27 PM