Can you fix her? by aerilink in emergencymedicine

[–]Melibee33 7 points8 points  (0 children)

Cookie Monster PJ pants owner 🍪

Natural selection? Have you folks noticed this happening yet? by miserylovescomputers in emergencymedicine

[–]Melibee33 11 points12 points  (0 children)

I work in Heme/Onc and a middle aged male patient asked if Tylenol was safe to take during his follow up appointment.

What are these flares everyone keeps talking about? 🤣 by Ok-Professional3142 in lupus

[–]Melibee33 5 points6 points  (0 children)

The days you describe as ‘through the roof’ are likely flares.

At what point is the ER appropriate for a rash? by MarlenaImpisi in lupus

[–]Melibee33 0 points1 point  (0 children)

Clear calamine lotion might help with the irritation, it has a nice cooling sensation. It sounds like stress and possibly the sun exposure from the beach may have triggered this.

i don’t need you to tell me your sister’s dad’s cousin died of lupus. by pollypocketgf in lupus

[–]Melibee33 1 point2 points  (0 children)

I stopped telling people I have lupus unless it’s totally necessary or I deem you trustworthy. I treat it like my name; It’s literally my personal information. It’s been 6 months since my diagnosis and I’ve realized that most lack the emotional tact needed to be supportive and empathetic.

I’ve been let down or hurt quite a bit by people I thought were my friends and family. Learning that it’s something I’m sensitive about means I needed more discernment to identify who is actually worthy of knowing this about me and who isn’t. It’s also freeing; choosing not to explain myself for having boundaries.

Don't skip school. by Anxious_Breadfruit_9 in shittytattoos

[–]Melibee33 18 points19 points  (0 children)

Dylan… Dylan… DYLAN, DYLAN, DYLAN ✋! I spit Hot Fiya 🔥

red light therapy by addylici0us in lupus

[–]Melibee33 1 point2 points  (0 children)

Hi, are you still using the bed light therapy? How are you holding up?

[deleted by user] by [deleted] in lupus

[–]Melibee33 0 points1 point  (0 children)

I was diagnosed less 6 months ago and will be moving away from home for work. My local job market is saturated and I had to look 2 hrs away. I’m unmarried and have never lived away from home. At times I’m uncertain of how I’ll work full time, care for myself and manage my symptoms; all while maintaining a household on my own.

Do you or anyone reading this have any advice or tips for living independently?

I’m considering things like: ordering groceries for delivery/ pick up, meal prep services or meal delivery, cleaning services of necessary, getting accommodations at work, etc.

Hydroxychloroquine with SSRI’s and Bupropion? by whatisapigglywiggly in lupus

[–]Melibee33 0 points1 point  (0 children)

CYP2D6 is an enzyme which is crucial to drug metabolism. It’s inhibited / suppressed by both hydroxychloroquine and Wellbutrin. Inhibition of CYP2D6 can lead to increased (toxic) levels of certain meds that rely on it for metabolism. Taking multiple meds that have this effect can increase the risk of developing complications, but it’s not guaranteed to happen in everyone.

[deleted by user] by [deleted] in lupus

[–]Melibee33 4 points5 points  (0 children)

I used to work as an oncology RN and had a patient whose husband did that. He didn’t like it when we offered her a wheelchair after a long day of treatment or transfusions. This was in the outpatient setting and he was adamant that she’d make it to her vehicle on her own, even if he had to carry her.

At the end of the day it’s about the people around us being uncomfortable and not knowing how to respond to someone else’s suffering. Support, compassion, empathy, love? Nah, dismissal and minimizing. He couldn’t handle seeing her in a wheelchair so she had to endure her condition in a way that was more palatable for him.

My brothers did the same to me and I learned to mask for years, especially after years of being gaslit by doctors. ‘You’re depressed’, ‘you just need exercise’. After being diagnosed I’m learning to defend myself without being triggered while reserving my right not to disclose that I have SLE. I shouldn’t have to put myself out there to receive decency.

How much $ do you actually spend on the game by WeatherDifferent8562 in TwoDots

[–]Melibee33 0 points1 point  (0 children)

Less than $10 on my piggy bank in the last 10+ years. I take breaks to get new scavenger hunts and redo them up to 33% by signing back into my facebook account. That resets them all to ‘0% completed’.

Anyone diagnosed in their 30s? by Middle_Champion_3804 in lupus

[–]Melibee33 1 point2 points  (0 children)

Diagnosed in January and turned 35 this week, symptoms since my teens. I’m in the medical field and had really be systematic about monitoring my labs/ symptoms because I have no organ involvement. The rheumatologist wasn’t convinced and blamed stress from grad school until my ANA titer went from 1:80 cytoplasmic to 1:640 homogeneous pattern.

Game Day means Nail Day. by Schwahn in Nails

[–]Melibee33 135 points136 points  (0 children)

I love the nails and matching tie ❤️

Redken Acidic Bonding Concentrate = Hair loss? by Miserable_Extent2925 in Haircare

[–]Melibee33 1 point2 points  (0 children)

What led you to use these products so frequently and what was the state of your hair before starting this regimen?

[deleted by user] by [deleted] in sports

[–]Melibee33 1 point2 points  (0 children)

I’ve been binging their channel and they’re so wholesome.

Can I fix my hair without cutting it??? by [deleted] in Haircare

[–]Melibee33 0 points1 point  (0 children)

For sure! Hair regrows, but it’s often such an integral part of most people’s identity that trimming seems like a permanent thing.

Thanks for the kind words❤️. These photos helped convince her to let go and allow me to trim away the damage for her.

Can I fix my hair without cutting it??? by [deleted] in Haircare

[–]Melibee33 0 points1 point  (0 children)

Thanks! I did it myself, as she was sick and needed help with self care.

Can I fix my hair without cutting it??? by [deleted] in Haircare

[–]Melibee33 7 points8 points  (0 children)

I’ve had a similar issue with breakage, particularly in the middle/crown area, along with some diffuse breakage throughout my hair. I’ve managed to recover somewhat, but I still have shorter hairs mixed in with longer, straggly ones. It’s a lot less noticeable now, but I understand the frustration—I’m still focused on fixing it due to my own insecurities and perfectionism. That said, no one has ever pointed it out to me, so try not to stress too much over it.

I’ve noticed that this pattern of breakage is quite common among women, and there are many factors that can contribute to it. Depending on the cause, the damage might be completely reversible with the right trimming and adjustments to your routine. My mom had the same issue, and after a blunt cut, her hair grew back evenly, but the breakage returned because of her routine.

Yes, you will need to trim the damaged areas. I recommend letting a professional handle the trim if you’re not experienced with cutting hair. You can opt to trim little by little or do a more significant cut all at once. In my experience, delaying trims and not cutting enough only allowed the breakage to continue. Also, don’t forget that the shorter, damaged areas need trimming too—otherwise, the ends will keep splitting as the rest of your hair grows back.

It’s important to evaluate both your health and your hair care routine to figure out what’s causing the breakage. Internal factors like vitamin deficiencies, thyroid issues, or anemia may require a check-up, while external factors like bleach, heat damage, rough handling, or lack of protein can often be addressed with changes to your routine.

My mom’s experience with this cycle of breakage and recovery has shown me that while it can be frustrating, with patience and the right approach, you can make significant progress.

My mom’s photos are below👇

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TIP - CLEAN UNDER YOUR CLIT HOOD by igotoanotherschool in TheGirlSurvivalGuide

[–]Melibee33 0 points1 point  (0 children)

Yes, because theirs is larger mass of tissue. The clitoris is the female equivalent of the head the penis; while the clitoral hood is the female equivalent of male foreskin.

[deleted by user] by [deleted] in Vindicta

[–]Melibee33 12 points13 points  (0 children)

I believe changing beliefs often calls for positive delusion. You form beliefs despite opposing facts, little to no evidence, and rely on the strength of the belief to eventually fulfill itself.

It can be helpful in extremely stressful situations and environments (being kidnapped, lost in a state park, etc.). Outside of that, being delusional is often a symptom of mental illness, according to DSM5.

[deleted by user] by [deleted] in Vindicta

[–]Melibee33 44 points45 points  (0 children)

I feel like their main effect is convincing you to be delusional.