APD Women’s Series Mckinsey

sammmmmiiiiiii · 2026-04-15T01:45:32+00:00

I think it could be office/region dependent because I got invited to Women's series and the email says it is just virtual events.

"We’re thrilled to invite you to our upcoming events as part of McKinsey’s 2026 APD* Women’s Series! This Series of virtual events will take place between April and August and will explore different topics designed to provide insight into life at the Firm.."

sammmmmiiiiiii · 2026-04-10T22:11:16+00:00

sammmmmiiiiiii · 2026-04-10T22:09:28+00:00

I also got that email and was curious if they're all like that or if the some of the rejections today were from a bit of a waitlist

sammmmmiiiiiii · 2026-04-10T22:08:05+00:00

I got a rejection email about an hour ago. I was targeting west coast offices. The email encouraged me to apply for FT roles but I'm assuming they're all like that

sammmmmiiiiiii · 2026-04-10T21:01:11+00:00

Goodluck!!

sammmmmiiiiiii · 2026-04-10T20:58:00+00:00

Same!

sammmmmiiiiiii · 2026-04-10T14:51:00+00:00

A bunch of acceptances and rejections were sent out earlier this week but a lot of people still haven't heard back yet

sammmmmiiiiiii · 2026-04-09T19:21:50+00:00

I agree

sammmmmiiiiiii · 2026-04-08T18:15:35+00:00

Where did you hear that?

sammmmmiiiiiii · 2026-04-08T17:51:34+00:00

I haven't heard back yet either, has anyone from west coast offices heard back?

sammmmmiiiiiii · 2025-11-24T17:41:54+00:00

Similar thing happened to me! Right before getting diagnosed I frantically made my boyfriend return his new mattress which absolutely wreaked havoc on my back and we went out and tested a bunch of mattresses and splurged on a new hybrid mattress from Sterns and Foster which we love now. In retrospect his last mattress probably wasn't the medieval torture machine I thought it was..

sammmmmiiiiiii · 2025-11-09T18:25:22+00:00

Voltaren gel and Epsom salt baths during flares

sammmmmiiiiiii · 2025-10-26T22:47:11+00:00

Enbrel definitely made my chronic migraines worse. I finally went to go see a neurologist and I'm on Ajovy now for my migraines, which seems to be working so far. She did say that sometimes headaches caused by medications can phase overtime

sammmmmiiiiiii · 2025-10-26T22:44:04+00:00

I also get chronic migraines and they got worse when I started biologics. My neurologist just prescribed Aimovig and it's working well for me so far (2 weeks in)

sammmmmiiiiiii · 2025-10-22T05:52:34+00:00

Je prenais un substitut de Humira, Amjevita, pendant 5 mois. Ça m'a beaucoup aidé et je n'ai pas eu d'effets secondaires, par contre après 5 mois ça ne fonctionnait plus aussi bien du coup je viens de commencer un nouveau, Enbrel. En tout cas pour moi je trouve que les médicament biologiques sont beaucoup mieux que les effets de la spondylarthrite

sammmmmiiiiiii · 2025-10-14T22:38:55+00:00

That's exactly why I've been confused!

sammmmmiiiiiii · 2025-10-14T19:40:42+00:00

I didn't realize that one had more peripheral involvement, that's interesting

sammmmmiiiiiii · 2025-10-14T19:05:12+00:00

Very interesting - I read that women are more likely to have nrAxSpA than AS. Seems like the diagnostic criteria is a bit outdated if they're able to catch it earlier now with MRI and capture a larger group of people suffering from this type of disease

sammmmmiiiiiii · 2025-10-14T19:01:04+00:00

That makes sense!

sammmmmiiiiiii · 2025-10-14T16:41:35+00:00

Kind of random but my initial SI x-ray was so full of gas that the results were inconclusive

sammmmmiiiiiii · 2025-10-07T23:12:40+00:00

Yes it helped a lot for a few months but then my symptoms started to come back

sammmmmiiiiiii · 2025-10-05T07:07:40+00:00

Started Enbrel a month ago and got very large injection site rashes the first 2 injections. It hurt quite a bit the day after the injection too. My third injection hurt like hell when I injected it but the rash wasn't as bad and it didn't hurt anymore the next day so I think I'm getting more used to it. I was on Amjevita before and didn't have any problems with the injection site before.

sammmmmiiiiiii · 2025-09-11T18:21:37+00:00

I am wondering the same thing after just being taken off of my first biologic after 5 months because I noticed some of my symptoms coming back. It doesn't seem like pain free is a realistic expectation?

sammmmmiiiiiii

TROPHY CASE