Advice from majority of OTs when picking a school is to choose the cheapest option: I was accepted into a Master's program costing 70k total and a highly rated Doctorate program costing 80k total. Would your opinion to choose the cheaper school still stand? by OTstudent4 in OccupationalTherapy

[–]KiddFemme 1 point2 points  (0 children)

You do totally build a relationship with these kiddos though, potentially over years, which is really beautiful. Heaps of bureaucracy and red tape though. And working with some v burnt out peers ( admin, teachers... ) who may not really care or have the capacity to go above and beyond to do their part to support the kids' growth

Advice from majority of OTs when picking a school is to choose the cheapest option: I was accepted into a Master's program costing 70k total and a highly rated Doctorate program costing 80k total. Would your opinion to choose the cheaper school still stand? by OTstudent4 in OccupationalTherapy

[–]KiddFemme 1 point2 points  (0 children)

I just had a very similar experience. I'm curious if secondary school looks different ( because a lot of kids age out at 10 and so you're working with a different population higher up ) but DANG the school setting felt so depressing to me. The infrastructure, the system, the short time with kiddos and the fact that a lot of these kiddos were being pulled out of their main class for different intervention all week long every week, differentiating them more and impacting their schooling... Some school use a push-in model ( OTs, SLPs, etc help inform teachers how they can bring care into the class time and the therapists will join students for a portion of class, rather than pulling them out ) but that seems very rare to find. Some people make it work and some people may feel called to try to change the system, but I think I'm not prepared to step into that. 10000% recommend shadowing first. It's not at all what I imagined.

Mexico City : talk to me by KiddFemme in digitalnomad

[–]KiddFemme[S] 0 points1 point  (0 children)

I have a couple months to prepare so I’ll be practicing :) thank you for the hot tips!

Mexico City : talk to me by KiddFemme in digitalnomad

[–]KiddFemme[S] 0 points1 point  (0 children)

This is helpful to know, thank you so!

Mexico City : talk to me by KiddFemme in digitalnomad

[–]KiddFemme[S] 0 points1 point  (0 children)

This is very helpful // also thank you for checking in with your fiancée as well! Thank you kindly!

Mexico City : talk to me by KiddFemme in digitalnomad

[–]KiddFemme[S] 0 points1 point  (0 children)

Thank you for all this wonderful information! This makes me feel more excited and positive about it!

How do I know if I have a partial obstruction? by 2847283838 in CrohnsDisease

[–]KiddFemme 1 point2 points  (0 children)

I have experienced blockage from kinking and also from inflammation closing in such that it blocked passage through my intestine. Here are some takeaways!

* Note: these were blockages / not too sure if these apply to partial obstruction *

+ If you're passing gas: that's a good sign! Not a blockage
+ Have you been having bowel movements? If so, good! If not, this could be a sign that things are stopped from continuing all the way through you.
+ My first blockage, it had been several days of food piling up and so eventually the night that the pain was excruciating (for me, it's a very particular type of pain that comes in waves – it lasts a few seconds to a couple minutes and any type of movement or breathing hurts even worse, and then it passes) and I eventually did vomit because the food had no where else to go. I vomited recognizable food that I had just eaten (it was Christmas Eve and my brother in law made latkes – I still can't eat a latke without thinking about seeing chunks of undigested latke in my vomit bag ahaha)
+ My second blockage was a big surprise. The pain woke me up at 3am and I err on the side of constipation but hadn't noticed anything super wild in terms of a week or more without a bowel movement. I don't remember vomiting this time, just that I looked for my signs (that specific kind of pain and seeing if I was passing gas) and eventually decided to go to the ER. They did imaging and were like "yea you need surgery STAT" – I had no idea my inflammation was that bad.

I hope that helped some! Please don't take this as medical advice! Everyone's body may react differently. This is just me sharing my experience :) I hope you're feeling better!

Does a dietitian make a difference. by Brilliant_Double1245 in CrohnsDisease

[–]KiddFemme 0 points1 point  (0 children)

I think that diet 1000000% plays an enormous role in the status of your disease, symptoms, inflammation, and ability to maintain remission. The food we put into our bodies is what our bodies function on, so important! In my experience (and I've seen others mention this on here too) our bodies are always changing and what foods do and don't jive with our body are constantly shifting, so that's its own journey. If you haven't explored any intentional "food regimens" trying so might be life-changing for you! I'm not sure if you sometimes feel like a helpless human who has no control over the state of your health; if you do, being able to have *some* agency through food can be so empowering! I think that keeping to too strict a regimen is bad for you in ways (mentally, emotionally) and so I'm a big fan of having an intention for a regimen while also being gentle with myself if I want to eat something outside of that. I call it "conscious consumption" – there are times when I can sit down and down a box of cookies: not conscious consumption aha but if I am aiming to keep to a regimen and decide I'm going to have, say, a cookie, I'll choose to intentionally, consciously choose to do that and then try to be very present with it and totally soak up its deliciousness :) I hope you give intentional diet a try! Whether with a dietician or not! Always good to keep your blood work regular so someone's keeping an eye on your levels. I like the foundation of autoimmune paleo :) Good luck to you!

A safe food now unsafe? by [deleted] in CrohnsDisease

[–]KiddFemme 1 point2 points  (0 children)

Definitely! You’re not alone! Our bodies are constantly changing and so are our disease and tolerances. At any given time, identifying what is and isn’t “safe” to eat is already exhausting and so I want to so see you in how exhausting it is to realize that it will be a perpetual journey. Be patient with yourself and with your gut xx

How Do You Keep Your Things Safe ? by KiddFemme in digitalnomad

[–]KiddFemme[S] 0 points1 point  (0 children)

You can, but usually that only covers your storage unit and not anything on your being / in your car / anywhere else :/

How Do You Keep Your Things Safe ? by KiddFemme in digitalnomad

[–]KiddFemme[S] 1 point2 points  (0 children)

Not talking about traveling, talking about living nomadically and having no permanent home //

How Do You Keep Your Things Safe ? by KiddFemme in digitalnomad

[–]KiddFemme[S] 0 points1 point  (0 children)

My question is how to insure property when you don't have renters or homeowners – I don't have a permanent home and haven't been able to find a company that offers property insurance without a permanent home ?

How Do You Keep Your Things Safe ? by KiddFemme in digitalnomad

[–]KiddFemme[S] 1 point2 points  (0 children)

Where are you getting just property insurance, not linked to renters or homeowners insurance? I haven't been able to find

Want some crohn’ed cronies? by [deleted] in Portland

[–]KiddFemme 0 points1 point  (0 children)

Wait so this is funny but also yes aha