u/TzwTzw

Hello guys once again, quick tldr I got diagnosed 2 years ago failed remicade like 3 months ago did my 3rd skyrizi infusion and now I'm gonna do the treatment thru injections in my house. My worst symptom is crippling fatigue and when I'm on my period I feel the whole going to the toilet multiple times a day. When I tell this to my doctor about the fatigue he says he can't really explain why I'm feeling like this due to my blood work being just fine and can't know why I feel like this, also when I tell him about my period symptoms he says I have to go to a gynecologist WHICH I WENT and he told me my Crohn's needs to get better for me to get better when I'm on my period but my doctor said that I have to get a second opinion. What should I do I'm pretty lost.

Hey everyone, fellow Crohnie here. I'm in the final stretch of my Master's in Applied Informatics and I'm choosing a thesis topic. Since I've been living with Crohn's myself, I want to combine that with my ML background and work on something like "Deep Learning-Based Pattern Recognition for Classification of Gastrointestinal Diseases and Inflammatory Activity in Endoscopic Images" basically training models to help classify GI diseases and flag inflammation severity from colonoscopy/endoscopy images. Has anyone here been part of a study using their scope images for research, or know of any public datasets I could use? Also curious if any of you work in ML or Data science or Software engineering and have thoughts on this from the patient side, like what would actually be useful for doctors or patients, versus what's just an interesting technical exercise. Appreciate any input, and thanks for reading this far!

In my case I have a bachelors in economics science and I'm finishing my applied informatics masters degree soon and I was wondering the strength of it in the job market.

Hey everyone, fellow Crohnie here. I'm in the final stretch of my Master's in Applied Informatics and I'm choosing a thesis topic. Since I've been living with Crohn's myself, I want to combine that with my ML background and work on something like "Deep Learning-Based Pattern Recognition for Classification of Gastrointestinal Diseases and Inflammatory Activity in Endoscopic Images" basically training models to help classify GI diseases and flag inflammation severity from colonoscopy/endoscopy images. Has anyone here been part of a study using their scope images for research, or know of any public datasets I could use? Also curious if any of you work in ML or Data science or Software engineering and have thoughts on this from the patient side, like what would actually be useful for doctors or patients, versus what's just an interesting technical exercise. Appreciate any input, and thanks for reading this far!

I got diagnosed 2 years ago, not in remission yet which saddens me a lot... I want to ask anyone else feels like they got stupider, like cant literally think, cant remember, cant keep up as they used to? Is it permanent? Is it gonna get better?

edit: it's important to point out that I have no deficiencies, it's just the stupid disease.

I started taking it a couple of days ago 40 mins before I sleep. At around the afternoon I have terrible abdominal pain but I'm not sure if it's from the magnesium, anyone else?

hello guys, I bought an RX 9060 XT 16GB some months back, I upgraded it from a 1650. The thing is when I open cyberpunk or deadlock my performance is just slightly better from the 1650. Cyberpunk for some reason regardless of setting my presets on low, medium or high or even tinkering with them, my fps reaches just 60 fps, most time even slightly below the 60 fps mark. Same thing with deadlock. My specs are:

Computer Type: Desktop

GPU: 16304MB ATI AMD Radeon RX 9060 XT (Gigabyte)

CPU: AMD Ryzen 5 3600

Motherboard: Micro-Star International Co., Ltd B450 TOMAHAWK MAX (MS-7C02) (AM4)

BIOS Version: American Megatrends International, LLC. 3.L0, 9/3/2025

RAM: 16.0GB Dual-Channel DDR4 @ 3200 MHz (16-18-18-38)

PSU: EVGA B5 650W 80+ BRONZE FULLY MODULAR

Case: 

Operating System & Version: Microsoft Windows 11 Home 10.0.26200 Build 26200

GPU Drivers: 26.6.4

Chipset Drivers: AMD B550 CHIPSET DRIVERS VERSION 8.05.04.516

Background Applications: DISCORD, HELIUM

Description of Original Problem: Low performance

Καλησπερα, έχω 70% αναπηρια και προκειται να κανω μια συνεντευξη για πρακτικη, καποιες μερες λόγω της αναπηριας μου δυσκολευομαι να σηκωθω απο τον πονο...κυριως τις μερες που εχω περιοδο που το κανει μη βιωσιμο εντελως μαζι με την παθηση μου. Αρα θα έχω σιγουρα μια φορα τον μηνα αδεια για να κανω την θεραπεια μου στο νοσοκομειο +2-3 τον μηνα... Πως μπορω να το συζητησω?

Καλησπέρα σας, είμαι γυναίκα 25 χρονών με 70% αναπηρία. Τελειώνω το μεταπτυχιακό μου στην εφαρμοσμένη πληροφορική και έχω προπτυχιακό οικονομικών επιστημών, θεωρείτε αξίζει να κάνω εισαγωγή με το 5% σε μια σχολή πληροφορικής, καθώς νιώθω πως δεν με κάλυψε το μεταπτυχιακό και δεν μου έδωσε αρκετά εργαλεία για να βγω στον τομέα εργασίας.

Καλησπέρα σας, είμαι γυναίκα 25 χρονών με 70% αναπηρία. Τελειώνω το μεταπτυχιακό μου στην εφαρμοσμένη πληροφορική και έχω προπτυχιακό οικονομικών επιστημών, θεωρείτε αξίζει να κάνω εισαγωγή με το 5% σε μια σχολή πληροφορικής, καθώς νιώθω πως δεν με κάλυψε το μεταπτυχιακό και δεν μου έδωσε αρκετά εργαλεία για να βγω στον τομέα εργασίας.

Just had a colonoscopy today, i failed remicade and im gonna start skyrizi any side effects i should know about?

Έχουμε κανεναν που να έχει? Αν ναι πως ακριβως την παλεύεται στην Ελλαδα με το συγκεκριμενο αυτοανοσο? Θα ηθελα κυριως να ρωτησω για το πως το διαχειρίζεστε στην δουλεια, ειναι μεγαλο μου αγχος τωρα που θα πρεπει σιγα σιγα να πηγαινω στο επομενο σταδιο.

Unfortunately after 1.5 year, remicade isnt really working for me and my doctor is gonna change my medicine to stellara what should I be expecting from the side effects?

my period has always been okayish, a lot of blood and a lot of days but not a lot of pain, I've been diagnosed with crohns nearly 2 years ago and my period has become more painful and its making me feel like my crohns is 1000 times worse. So I'm thinking of going to my gynecologist and start talking about BC, is it worth it with the side effects, i dont have acne and my period is coming precisely every month, am I gonna fuck over my hormones?