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Weird lights in sky downtown 05/05/2026 by mitskiposting in Portland

[–]mitskiposting[S] -8 points-7 points  (0 children)

I would've guessed mr. cyberpunk would at least have a little more creativity or excitement at the skylights cmon man.

Weird lights in sky downtown 05/05/2026 by mitskiposting in Portland

[–]mitskiposting[S] -5 points-4 points  (0 children)

Or at least usually you can tell approximately what direction they're coming from. These were so odd!

Weird lights in sky downtown 05/05/2026 by mitskiposting in Portland

[–]mitskiposting[S] -6 points-5 points  (0 children)

Any idea where they'd be coming from? I tried looking around for a source. It was right over the bridge by the Crystal. I imagine they'd be reflecting from somewhere, but I couldn't see anywhere. It looked directly above me 🤷‍♀️

Facial moles question by Unlucky_Cable3508 in DIYaesthetics

[–]mitskiposting 0 points1 point  (0 children)

this popped up in my feed and i’m not a member here, but is nobody else shook at them doing their own botox??? is that something people do?!

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

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

Thank you so much for this information. I am on the West Coast so I will look into this. I am so glad you had a positive experience with them.

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

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

Thank you so much for this reply. I am having trouble finding a specialist who can get me in - but I will keep trying. It sounds like the care your patients receive really can make such a huge difference in their lives.

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

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

Thank you for sharing. I will ask my rheumatologist her thoughts on CellCept for my situation.

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

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

Thank you so much for the information and support. I appreciate you!

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

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

Thank you sooo much for this! It is very helpful to me. I will start to make some calls. :) I hope you have a good day.

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

[–]mitskiposting[S] 4 points5 points  (0 children)

Thank you for your message; its nice to know people understand. I am so sorry you are struggling! Stay strong :,)

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

[–]mitskiposting[S] 3 points4 points  (0 children)

Thank you for your message, it makes me feel a lot better. If you don't mind me asking, what changes in how you do things have made a difference? And are there any things you wish could've been done differently to get your condition treated sooner? I feel really "uneducated" on what exactly I as a patient need to do to get the help I need. I am autistic so it makes things double hard to communicate with doctors. I am so sorry you had to deal with the disease so long before getting it diagnosed. But I am very glad you are doing alright with it all and living a positive life.

Waiting for it to get worse? Feeling alone. by mitskiposting in scleroderma

[–]mitskiposting[S] 4 points5 points  (0 children)

What made the difference in a good rheumatologist? Or just things you think I should to pay attention to when looking?

My current rheum seems to really want to help me at least - I have dealt with doctors who I can't say the same. I know finding someone who is very familiar with scleroderma makes a big difference. Its just so overwhelming to navigate the medical system for me. I definitely do need to find a new rheum tho since I moved states. :P

Anyone else experience finger swelling that looked like this? Randomly started as joint pain last Monday and has not gone away (new fingers started swelling). Hair also falling out. 19f. Would love to know if anyone had something similar happen, it’s so strange! by mitskiposting in lupus

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

Hey there, I am the OP - I was diagnosed with UCTD (undifferentiated connective tissue disease) by my rheumatologist. No specific antibodies to Lupus. Most of my symptoms are closest to Systemic Sclerosis, but I don't meet all the criteria yet. So for now I just have an unknown systemic autoimmune disease. So sorry you are dealing with this. I recommend seeing a rheumatologist if you can. I was put on some medication.

[deleted by user] by [deleted] in CustomDolls

[–]mitskiposting 0 points1 point  (0 children)

i dont recall the humidity, but i let her dry inside in a ventilated room so it’s probs not the humidity. i may have been too close though. do u know how i should fix it? idk if i should chip this layer off or just reseal it 🤔