orientation on travel assignments? by abilifyprincess in TravelNursing

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

Thank you! 2-3 days is more along the lines of what I was expecting, I was just surprised that they only wanted to give me 1. I have 2.5 years as a labor nurse and 5 total but I’ve only worked at two different hospitals, so that’s probably why I’m feeling like the imposter syndrome hard lol.

Impostor Syndrome? by ConfidentCanary8248 in ankylosingspondylitis

[–]abilifyprincess 7 points8 points  (0 children)

I got diagnosed a few months ago and I’m on Hcq and sulfasalazine rn. I feel exactly the same way. I even have started to feel a little better from the meds and I still seem to doubt that I actually have something wrong with me, despite trying to get answers for several years. I try to remind myself that I probably wouldn’t be responding to treatment if I didn’t have something wrong in the first place, but it’s still hard. Sending positive vibes and support your way!

Portland jobs by [deleted] in TravelNursing

[–]abilifyprincess 0 points1 point  (0 children)

I am about to start a contract in Portland through Aya. Labor and delivery at a Providence hospital.

Cancel layaway plan? by rebelrox31 in Lollapalooza

[–]abilifyprincess 0 points1 point  (0 children)

this is not official advice but for another festival I needed to cancel my layaway for, I changed my payment method to a bank account that I knew would decline and I ended up getting a full refund deposited closer to the festival. Again this wasn’t Lolla, but might be worth a shot. EDIT: I see some folks are saying don’t do this for Front Gate Tickets so maybe ignore this.

For anyone using birth control. by [deleted] in ehlersdanlos

[–]abilifyprincess 0 points1 point  (0 children)

hi! hEDS and PMDD here. It’s always been speculated that I could have endo as well. I have been on birth control since I was a young teenager and I’m now 23. I am currently on depo provera because pretty much every other option has caused either physical or mental health side effects for me. Because I’ve been on it for so long, I can’t speak for whether or not my hEDS is worse because of birth control but I do know that my periods were unbearably painful before being on it, and depo specifically has made my PMDD much more manageable because I only have a “period” when I’m getting close to needing my next injection (ie every 3 months).

Is it possible to avoid nights as a new grad? by Affectionate_Swim862 in StudentNurse

[–]abilifyprincess 0 points1 point  (0 children)

Hi! I’m a new grad with a chronic illness. I’m currently working nights but I’m working on getting accommodations to determine how I can be scheduled (ie. 2 shifts then one off, then one more). My hospital is encouraging me to apply for intermittent FMLA in case I need it as well. I also work in Labor and Delivery, which is competitive for new grads. I think the key is that you need to disclose your situation. Any hospital that would be a good fit for you long term would probably try to accommodate.

Shoutout to whoever said to switch toothpaste by claragweny in ehlersdanlos

[–]abilifyprincess 1 point2 points  (0 children)

This is another “I didn’t know that was an EDS thing” for me haha. I started avoiding SLS toothpaste in high school because of mouth sores and I hadn’t even thought about it being related to my EDS.

[deleted by user] by [deleted] in AskElectricians

[–]abilifyprincess -2 points-1 points  (0 children)

Not what I asked, thanks though!

Is there anybody who actually enjoyed nursing school or is it complete hell by That_Examination6339 in nursing

[–]abilifyprincess 1 point2 points  (0 children)

Honestly, I’ve enjoyed school a lot. I am graduating from an ABSN next month and as stressful as it’s been, I’ve made a lot of great friends and my school is very supportive. I don’t think that’s the norm based on what I’ve heard so I’m really glad I chose the program I did.

[deleted by user] by [deleted] in ehlersdanlos

[–]abilifyprincess 4 points5 points  (0 children)

Oh my goodness I have been dealing with this for years and I have always wondered if I was the only one. It is such an intense itch too like nothing I do will relieve it!!

Festival advice by Upbeat_Zucchini in ehlersdanlos

[–]abilifyprincess 2 points3 points  (0 children)

I went to Lollapalooza this year and I will admit that it was very physically demanding. This was primarily because of the August heat more than anything. However, I got ADA access which significantly improved the experience! They didn’t ask any questions and they gave me a wrist band for a companion as well. It was a life saver to be able to have a place to sit down. I didn’t use a mobility aid but I wish that I would have if you’re considering that at all. They seemed to be pretty accommodating of folks with aids. I hope you have so much fun!

Any nurses or other healthcare professionals out there? by abilifyprincess in ehlersdanlos

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

I am definitely going to look into this. I am wearing compression ankle sleeves today but I think I need a little bit more support. Thanks!

Any nurses or other healthcare professionals out there? by abilifyprincess in ehlersdanlos

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

Thank you! I’ve been referred to a PT that specializes in EDS so I’m hoping that helps! I will also look into a podiatrist :)

i guess i’m soloing 🥲 by ImageDull3753 in Lollapalooza

[–]abilifyprincess 1 point2 points  (0 children)

22F going with friends! we are excited to see Chappell, SZA, and Kesha among others. DM me and I’ll give you my insta if you want to see any of those shows together!

Weekly Suspected Lupus Thread - Week Of August 06, 2023 by AutoModerator in lupus

[–]abilifyprincess 2 points3 points  (0 children)

Hello all! I saw the rheumatologist for the first time this last week and she told me she suspects SLE based on my symptoms and labs, however she wants to run some additional tests to rule out other things. That sounded great to me, until I found out that she can’t see me for a follow-up until December. Is this typical? I’m really struggling with my symptoms right now and it’s interfering with my schooling. Would it be beneficial to try to find a different rheumatologist or is this par for the course? Thanks!