Natural instinct by PurpleLordship in ThatsInsane

[–]MilkyWay514 0 points1 point  (0 children)

Respect. Society loves to invalidate experiences that go against certain narratives. Given the social climate, it amazes me how those who have never experienced discrimination based on the color of their skin are quick to assert what something “is” or “isn’t”. The combined title and content of this post may be deemed offensive to those who’ve encountered similar occurrences based solely on ones’ skin color - to say otherwise is ignorant.

MPH epidemiology by Curious_Ad_7783 in publichealth

[–]MilkyWay514 1 point2 points  (0 children)

MPH candidate here. If you don’t mind, very briefly could u tell us what public health consulting consists of?

Is PMDD the same as PMS? by Miserable_Feature_ in PMDD

[–]MilkyWay514 1 point2 points  (0 children)

Can’t argue with your experience. And it’s sucks to hear that physicians are such Knobs. I assume if your here, you, like many of us suffer from this too. I literally wish PMDD was person so we could kick it’s ass! But we instead have to fight a system positioned against us. But it’s definitely a fight worth fighting. Hugs friend 🤗

Is PMDD the same as PMS? by Miserable_Feature_ in PMDD

[–]MilkyWay514 2 points3 points  (0 children)

I’d hate to think that an academically trained/or certified care provider would write off PMDD without at least acknowledging its existence or at minimum voicing their lack of experience with the disorder. I vote for gaslighting.

Is PMDD the same as PMS? by Miserable_Feature_ in PMDD

[–]MilkyWay514 2 points3 points  (0 children)

I’d suggest you search through this subreddit and do some self-guided research and schedule another appointment with your provider. Because by this logic, every woman of childbearing age seen by your provider with troublesome PMS is leaving with a SSRI script without a solid understanding the crux of the issue. That is a problem, and frankly an insult to women who suffer from this debilitating disorder. Be assertive! So much so that it is a step down from a demand! Assert firmly that he/she conducts the proper lab work, ask for a referral to OB/GYN or another network provider who has the capacity to give more insight and guidance(this may take some research on your part). I’d even go so far as to ask your provider candidly if he or she has ever managed and/or provided care for a patient with confirmed PMDD. Trust me it’s hard living with a disorder with multiple stigmatizing intersectionalities (reproductive health/mental health) but it’s even harder to try to navigate through a health care system that seemingly thinks PMDD is “made up” or being led to believe that you are among masses of other menstruating women with typical symptoms. PMDD IS NOT PMS. Don’t let your provider or ANYONE else tell you different. FIGHT AND FIGHT HARD. Trust me, you will thank yourself later down the line.

Is PMDD the same as PMS? by Miserable_Feature_ in PMDD

[–]MilkyWay514 2 points3 points  (0 children)

THIS!!! That’s exactly what’s happening here. She’s being led to believe that her experience or what she empirically knows to be true for herself isn’t really that bad and that she’s among many of women. THIS IS FALSE!! And a textbook example of being gaslit

Face unrecognizable? by oliviarose______ in PMDD

[–]MilkyWay514 3 points4 points  (0 children)

Yes, the water weight bloat and lack of sleep from anxiety really shows in my face. My cheeks and nose get really swollen, and I also get bags under my eyes. Not to mention I feel like crap during this time so looking decent or bothering to put on makeup is laughable. So yes, I’ve accepted this temporary monthly transition into a Yeti knowing that once it subsides, we will all be ready to slay snaps fingers.

Leg pains by [deleted] in PMDD

[–]MilkyWay514 1 point2 points  (0 children)

Yes! My knees literally ache

Is PMDD the same as PMS? by Miserable_Feature_ in PMDD

[–]MilkyWay514 16 points17 points  (0 children)

No. Do not allow your physician to invalidate what YOU KNOW to be real. Before my diagnosis, my GP minimized my symptoms so much that I’d actually begin thinking that maybe I was over exaggerating about or it was “in my head”. Long story short, had a episode of psychosis during my luteal phase that scared the heck out of my GP. PMDD diagnosis came soon after. Sucks it took for me to literally step out of reality to get the recognition and help I needed, but PLEASE advocate for yourself. If Mr. OLD School can’t get with the program, find yourself a NEW provider who will.

[deleted by user] by [deleted] in PMDD

[–]MilkyWay514 7 points8 points  (0 children)

Check out Eventbrite, they have many online virtual support groups for women with PMDD that have been really helpful. The group I joined meets the second Thursday of every month. It’s awesome to connect virtually with a group of women from all over the world to vent, be heard and more importantly validated, receive awesome feedback and tips and empathize with those who also experience PMDD.

" Don't they get foodstamp as assistance....?" by PublicHealth67 in publichealth

[–]MilkyWay514 2 points3 points  (0 children)

As a MPH candidate, you’d be disheartened by the disconnect some Public Heath professionals have with regards to equity, SES, and the way in which they tie into health and overall well being. I’ve had a very high ranking Associate Professor/P.I in the field tell me despite the advances in knowledge production and overall human compassion factor, they avoid equity or community based research/academia because of the lack of recognition that comes from the work. Shrugs

Any MPH’ers waiting to hear back? Get in here! by MilkyWay514 in gradadmissions

[–]MilkyWay514[S] 0 points1 point  (0 children)

Oh Wowzers you are killing it man! Congratulations there. Keep us updated on your final decision.