#crohnie

[existennialmemes]

Me: [eats a food that will give me a tummy ache]

Me: [gets s tummy ache]

Me: Interesting Result.

Me: [eats it again, gets a tummy ache again]

Me: And consistent too!

Me: [eats it again, gets a tummy ache again]

Me: Well what's important here is that we're getting some very reliable data.

[dr-sunshine-md-is-me]

The horrors (tummy ache) persist yet we (me my self and I) venture forth with the power of friendship (sprite saltine crackers and tums)

[pluckedanarchist]

"This colon waits for no man."

-real thing I said to @azraeldigabriel

[progressblog]

What's your experience with Crohn's, if you don't mind (curiosity)?

Hi @hauntedmoontimetravel !! Lovely question but took me hours to write lol.

Crohns disease is chronic and an invisible illness like any other autoimmune condition and my intestines are effected by this.

On a day to day basis:

When in remission that is having no active symptoms

- i face joint aches (nowadays its ankle aches and back neck ache)

- less energy (so i sleep a lot more than people usually do typically 9 hours daily) and as someone who gets periods this gets worse during those days

- getting tired easily

- cant do any intense activity or else ill vomit

- dietary restrictions (majorly omelettes or any egg dishes other than boiled eggs but there are more like cauliflower makes me gassy and dairy except yogurt gives me pimples and sometimes rarely nowadays loose stool…) if i eat such items then i end up vomiting, having acidity or acid reflux and have stomach ache that would hurt like someones trying to rip apart my organs and even lower energy

- In general i keep in check my intake of refined/white flour and fried items although currently been eating a lot of chips because it feels good like its a stress buster.

- Another is i cant go long without eating otherwise i get stomach ache and start feeling like even more low on energy so if i had lunch at 2pm after 4hrs i need to eat at least something but more than say 2 bananas.

So you can see it isnt that severe unless i eat outside meals then I’ll get sick easily and frequently so only home cooked meals are preferred.

When Stressed:

When im stressed my appetite immediately drops also during periods which is also stressful and i literally dont feel like eating more than 1 meal a day but i do eat 3 meals just very less in quantity. Thats how i know im at my worst mentally.

Management:

So on a daily basis for management i take immuno suppresants 1gram of mesalazine (it has the least side effects of all the immuno suppressants) 3 times a day after each meal also folvite and sompraz on empty stomach each morning for stomach acid and i dont take any supplements currently but i was put on and off on vit D3 and iron tablets. Personally, i think im still low on iron lol.

Main Struggles:

The thing about autoimmune diseases is that once you get them you easily are at risk for other chronic diseases especially as a woman the list is even longer. Thankfully, i dont have any other disease other than this and some mild ent related issues.

So, my biggest struggle is with stamina, (im always out of breath climbed 1 floor of stairs out of breath…), exercise, pain tolerance and bone health. Sometimes i feel like this is regular ache and takes me time to realise theres nothing known as regular ache lol and somethings off. Its due to getting tired easily that its hard to stay consistent with exercise so i have gained a lot of weight in past 2 years (also cuz of anti depressants). This puts me at risk of other chronic illnesses as well ugh this is endless.

Anyways, due to my immune system being suppressed constantly my lymph nodes are always swollen and im at risk to catch communicable diseases easily in comparison to people with proper functioning immune system and wound healing is slow.

Check ups:

I need yearly check ups so each year i get tested for inflammation (which is never below 100 if autoimmune) mine was 300 last i checked about 2 years ago (last year i procrastinated) due to stress (that year i dropped out from law school and had a break up …) and deficiencies (blood work) and get colonoscopy to actually see how are the insides of my intestines.

About colonoscopy, it requires a prep so i prefer to get admit because it makes me feel so weak that its not possible for me to take stairs or speed walk. Essentially this laxative (of 1L horrible tasting) makes you go to bathroom for about 15 times to a minimum of 7. So to stay hydrated so that i dont pass out everything i take fluids via iv when i do get admit.

During flare ups:

There are other symptoms that show up if i not in remission or having a flare up (if i dont take my meds or the meds arent enough or have stopped working) such as weak eye sight and the white in the eyes becoming off white and even lower energy levels that even walking gets hard due to constant stomach pain many antibiotics, anti acid… and all stop working and over time due to diarrhoea and vomiting i end up losing weight and become anorexic it gets so bad that i lose 2kgs a day to 4kgs.

So ofcourse i need to get admit in such cases and be put on corticosteroids and this medicine has A LOT of side effects and makes you immunocompromised.

Vegetarian dietary nutrition taken almost everyday:

- coconut water/electrolytes especially if i exercise

- cultured plain white yogurt with lunch and dinner for probiotics

- protein like white rice (although has more carbs), lentils, split mung beans, kidney beans, pigeon peas, black chickpeas

- green tea for antioxidants unless i have brain zaps

- for fibre i take chia seeds/fibre biscuits/fruits or psyllium husk only if im constipated

- for fatty acids i take one spoon of plain non roasted flaxseeds (need to start taking them again)

- For iron 5 dates (need to start taking them again) or dates syrup as a sweetener

- others - puffed whole wheat flatbread not daily, at least 1L water but i aim for 3L, dark chocolate and meds

- cheat items been consuming recently - peach flavoured sparkled water, Vietnamese cold coffee and chips.

[bass-alien]

been a rough last few days, stayed home from work yesterday and am going into work late this morning, sending so much love to anyone who’s also dealing with chronic pain and/or not feeling so great right now

[artistatthedisco]

Crohn's Disease

click for detail

[david-goldrock]

I am happy to announce, that my last medical checkup results are in, and I am in complete remission of Crohn's disease

[diningwiththeasquiths]

6 selfies of 2024

A hike in the snow in January

A train ride in March. Read this fun and fascinating book called 'The Last Spring of the Dinosaurs' by awesome paleontologist Melanie During (also had the pleasure of attending a lecture of hers this year)

It's giving 'Girl Who Is Going To Be Okay', but in actuality the sun was shining in my eyes during this hike in April 🤣

More dinosaur shenanigans in a Hannover museum in October 🦖

My solo album cover 😝 Made during a trip to Scotland in October

And lastly, from that same trip, the kind of big dick energy that I would like to exude more often 😎😂

Started this year pretty depressed. Luckily I received help and am definitely mentally in a better place at the moment. Will continue seeing my autism life coach for at least 10 more months, because my self-esteem is still extremely low and impacts everything else.

Healthwise I finally had bowel resection surgery this year! 🙌 I really hope I'll be able to get by without any Crohn's medication for a few years at least 🙏 They told me I'll be getting an endoscopy in January, so we'll see.

(I also sought help for my excessive hair loss, and my scalp has since improved. Hopefully my hair will become a bit more full again 🥺)

And I've been thinking about dipping my toes back into fandom servers on Discord. Been avoiding it because my social anxiety is pretty severe. But I also miss it 🥺

So if anyone knows a friendly IWTV Discord server that's relatively small and low-key, please let me know! ❤️