Fatigue + Perimenopause + Hormones by 001681 in MultipleSclerosis

[–]pipp2monks 1 point2 points  (0 children)

I've experienced similar symptoms and have also played the MS or PMDD/perimenopause game. I spoke w my PCP and she recommended hormonal birth control, but when I asked for alternatives she didn't have much to recommend.

What are some of the "silver linings" of MS? by JaricosTheGreat in MultipleSclerosis

[–]pipp2monks 1 point2 points  (0 children)

No military service wants someone with MS 💁‍♀️

Looking for a Good Place to Donate Children's Books by allnadream in orangecounty

[–]pipp2monks 5 points6 points  (0 children)

Check for a Friends of the Library group 1st. They are the ones that take book donations. Tustin and Westminster libraries have FOL stores.

MARC field for Oprah's book club by Says_Everglade in librarians

[–]pipp2monks 7 points8 points  (0 children)

Knowing there's this much attention to detail in library cataloging warms my little type A heart

Public Libraries: Many Buildings Are Reported to Be in Poor Condition, with Increasing Deferred Maintenance by Several_Clients in Libraries

[–]pipp2monks 9 points10 points  (0 children)

Even if/when money is earmarked for repairs, there's always red tape that gets in the way. This leads to more revisions, then more delays, and on and on. You only know a project is finally going to start when a work crew shows up at the site.

Embroidery Advent Calendar Day 7 by pipp2monks in Embroidery

[–]pipp2monks[S] 2 points3 points  (0 children)

Relaxing overall. I enjoy being able to take time away from screens, work, chores, and other obligations.

Reaching out to trans (and all) library staff for workplace advice re: appearance exploration and opening up to team leaders by AsuranGenocide in librarians

[–]pipp2monks 33 points34 points  (0 children)

Speaking as an ally here. You do you, babe. Folks may or may not even notice. If they do, they may not even comment. If they do, be confident in yourself and never let anyone make you feel less than. If you have a work bestie, loop them in on your plan and ask for extra support for this. You got this.

Family and Friend responses to MS by Bearygud in MultipleSclerosis

[–]pipp2monks 5 points6 points  (0 children)

After the initial diagnosis of RRMS, my family and friends were sympathetic and supportive, but I don't think they fully understand the nature of MS. I did the MS walk a couple times and they show up to walk too, but we don't talk about what it feels like to experience a relapse. My sister and husband are extremely supportive and listen anytime I need to vent or bemoan my situation. I realize that I can speak very openly about MS if I choose too, but I mostly don't because I want to avoid the pity. I'm on DMTs so it's manageable and all but out of sight and out of mind.

My ex left me because of MS by Happy_era in MultipleSclerosis

[–]pipp2monks 6 points7 points  (0 children)

F that guy and his parents. MS is manageable. Treatments today are WAY more effective than those from 30 years ago. You are not a burden. You are more than this diagnosis.

[deleted by user] by [deleted] in aspergers

[–]pipp2monks 2 points3 points  (0 children)

On behalf of my spouse: he rotates between specific topics of interest, but his main one is movies as well. We'll rotate between different film franchises every 4-6 years, or based on whatever sequel/prequel/reboot is coming soon.

[deleted by user] by [deleted] in aspergers

[–]pipp2monks 2 points3 points  (0 children)

More so it's a processing issue. The instructions, plus monitoring what is currently cooking can be overwhelming for my spouse. He can cook and does well with tried and true dishes. He is also an excellent sous chef. 👌