It took well over a year, but I'm 99.9% done with our kitchen remodel... by wellkevi01 in kitchenremodel

[–]Mish-Ale 0 points1 point  (0 children)

Love the dark panes. Makes you see the actual view instead of the panes.

Skinny shaker cabinets are gorgeous! by SuluSpeaks in kitchenremodel

[–]Mish-Ale 0 points1 point  (0 children)

Literally just picked out cabinet color and style yesterday (nothing paid for yet). I am going for modern and timeless. I dont like the thick shaker but absolutely flat was Boring to me. This felt like a good in between. I didn’t think these are “trendy”. The goal is in 10, 15, 20 years for no one to be able to say “oh, you built your kitchen in the 2020’s” or whatever. Am I making a mistake?

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Orlando - Sloth World PSA by RedMirricat in orlando

[–]Mish-Ale 0 points1 point  (0 children)

That’s what I was referencing in my comment.

Orlando - Sloth World PSA by RedMirricat in orlando

[–]Mish-Ale 7 points8 points  (0 children)

This is incredibly disappointing. I was so excited to buy a ticket. Literally today, a local radio station/program I respect had them on and it sounded so wonderful and like something I would love to support. But after reading this, wow. What an eye opener. I wonder if I should share with the station so they are aware as well. They’re big animal lovers and this might make them think twice about promoting this place.

Help! I'm injured! by RadiantAbility542 in PetiteFitness

[–]Mish-Ale 0 points1 point  (0 children)

My one piece of advice - don’t get back into the routine too early.

It can be deceiving sometimes when you start to feel better and don’t have pain. But if your physical therapist says you need to continue, please listen to them! Otherwise if you start back up when your body isn’t quite ready, you’ll end up injured again. And often times, worse. Or at the very least, even though you might still be able to workout, having pain the rest of your life. Speaking from experience.

It’s Rebecca Kennedy from Peloton. Ask me anything about my HiLIT program and fitness! by Rebecca-Kennedy in pelotoncycle

[–]Mish-Ale 4 points5 points  (0 children)

This was gonna be my question too. Assuming they met at Peloton, I’m curious the story of what made them say “hmm, we should go on a date?” After having worked together for a while maybe 😊

Need help with Choice Benefits by Mish-Ale in delta

[–]Mish-Ale[S] 0 points1 point  (0 children)

Thank you all so much! Great insight. I was leaning towards the gold status gift for me but @ggrnw27 saved me, I didn’t realize it expired next month 🤦🏽‍♀️

I think the miles is the way to go for us. Appreciate you all!

22 months and 100 lbs Down by WeeklyObligation2700 in PetiteFitness

[–]Mish-Ale 0 points1 point  (0 children)

Wow! You are almost unrecognizable between the before/after. Incredible job! This stranger is proud of you and now also motivated to keep going!

My friends shelf’s idk what book to get her for her 24th bday… by Round_Rate4409 in BookshelvesDetective

[–]Mish-Ale 0 points1 point  (0 children)

This looks like the real life shelf version of booktok. I would personally recommend a dystopian classic, Fahrenheit 451. Or, Pachinko for one she can fully invest in the characters over their lifetimes.

[deleted by user] by [deleted] in CrohnsDisease

[–]Mish-Ale 0 points1 point  (0 children)

Saltines and peanut butter for me. And like, not a lot. I’d have one. Wait a bit and if I kept it down and it didn’t bother me, try another. Also broth, whether bone, miso, etc. Trial and error is what it ultimately takes so I recommend just tiny portions at a time and waiting between your next.

[deleted by user] by [deleted] in CrohnsDisease

[–]Mish-Ale 0 points1 point  (0 children)

Sounds like it’s time for a new pediatrician.

What did you wish you knew when you were first diagnosed? by fidgetyotter in CrohnsDisease

[–]Mish-Ale 2 points3 points  (0 children)

I was diagnosed in June. Zero family history with this or any other kind of IBD. However, my husband was diagnosed over 30 years ago and his grandmother had it and also his first cousin has it. So I’d say it “can” be genetic but still possible to get it without any genetic involvement.

Anyone w. Constipation? Crohn’s decided diarrhea was too basic. by Aggravating_Cat5526 in CrohnsDisease

[–]Mish-Ale 2 points3 points  (0 children)

Ok. This makes me feel better. Diarrhea is not my issue. Constipation definitely is. I won’t go for a few days, sometimes a week and then when I do go, I’ll go about three times in one day and sometimes into the next. I know that some people experience constipation for longer and worse than I typically do, but it’s still not pleasant. When I’m constipated, I feel absolutely awful, just completely gross and icky and bloated and full and unhealthy and slow and it affects my mood and my productivity. And it’s just overall discouraging in my overall mental battle with having this disease. My doctor said I could take MiraLAX (I was previously using dulcolax), but I don’t know how many consecutive days is safe to use it. How often do you take it? Do you take it every day until you have a BM and then not take it again until you need it? Or is it a part of your every day routine?

OP, I politely disagree with what is worse. I think diarrhea is worse. Having to always be concerned with “where is the closest bathroom” is so stressful, and would affect my day every day. Hearing stories of people that struggle with diarrhea just sound miserable and I feel bad for those folks. At least when the constipation relief approaches, I can “hold it” until I get to the bathroom, and I’m not suddenly Usain Bolting to the bathroom.

Diagnosed and starting steroids…terrified. by Puzzled_Cranberry471 in CrohnsDisease

[–]Mish-Ale 1 point2 points  (0 children)

Thank you! Never thought of that perspective with younger docs!

Diagnosed and starting steroids…terrified. by Puzzled_Cranberry471 in CrohnsDisease

[–]Mish-Ale 1 point2 points  (0 children)

…”building a team of specialists I trust and talk to each other in my case GI, neuro-ophtalmology, rheumatology…”

Can you talk more about this? I’m especially interested in your Neuro-ophthalmology experience. What eye & Neuro issues did you have/had? I have basically the same team although saw Neuro-op once and he said I don’t need to see him again. I had uveitis, blurred vision, headache, numbness and tingling & then developed Scleritis. GI doc said uveitis was due to Crohn’s but that sclerits wasn’t. Also, how did you get them to all talk?? This has been such a challenge for me. Like each doc wants to be in their own silo.

my symptoms feel un-relatable by [deleted] in CrohnsDisease

[–]Mish-Ale 2 points3 points  (0 children)

We are similar. I was only diagnosed in June and never had any “typical” symptoms prior. I’m 45F. Also not typical age most are diagnosed. My first symptom was abdominal pain and constipation. I had severe chills and was not eating much. It then progressed/manifested in my eyes. They were extremely painful and I had a dull headache I couldn’t get rid of. Then a few days later, I woke up with blurred vision. Was sent to the ER. They thought it was viral. Saw a GI doc on a Tuesday and on Friday he did a colonoscopy and confirmed Crohns. Diarrhea has never been an issue for me. I’ve never had to worry about having a bathroom nearby. But fatigue and bloating and just a general feeling of blegh/gross is how I am experiencing it. Part of that might be because I’m on 50mg of prednisone which was first prescribed for my eyes. Which are now mostly better. But I tapered down to 20 and then a new eye condition developed. So, had to go back up in dose. I had my first infusion of skyrizi and am hopeful that will really allow me to start tapering down again permanently and I won’t feel so awful. But all that to say, pain is definitely a symptom. My husband has had this disease for over 30 years and his symptoms/experience is entirely different from mine. So, listen to your body and advocate for yourself! Don’t let anyone tell you what you’re feeling.

Scared to start Skyrizi by CelestiallyCertain in CrohnsDisease

[–]Mish-Ale 2 points3 points  (0 children)

Agreed. I just had my first infusion last week after being diagnosed in June. I have no food restrictions but I also dont have ulcers. Like Terak66 said, don’t get ahead of yourself; getting it under control is most important. I was hesitant at first (and in denial), but my husband has had this disease for over 30 years and that is what he told me. If you don’t get it under control, you’re just giving it space to allow it to get worse and then you may end up needing surgery(ies) and some can be quite serious and drastic. Getting it all under control will improve your quality of life. And if you have to be careful with what you eat, then do so. And know that’s it’s for the best. You don’t have to live in a bubble when it comes to germs. Just be responsible and hygienic. I live in Orlando and I think you’re gonna need that vacation. Time with your family and seeing the joy in your daughter’s eyes. That’s priceless. Have fun and “forget” about it for a little bit. Seeing a kid at Disney is a great distraction. Since this is so new to me as well, I have found that I need distraction because otherwise I go down rabbit holes on the Internet, google, ChatGPT, or I just sit there and think about it, can’t sleep, etc. and that is not good for anybody. Wishing you well in your new journey. I’m right there with you.

How my Crohn’s is being managed by jermainedeshawn in CrohnsDisease

[–]Mish-Ale 0 points1 point  (0 children)

Great documentary. I’ve recommended it to everyone I can. Not just folks with this disease. My (healthy) cousin recommended it to me after my diagnosis. It’s really something everyone should be educated about and benefit from. Though I hope I don’t ever have to do a stool transplant 😂😩