polycystic ovarian syndrome

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    Spironolactone for #PCOS ?

    My endocrinologist appointment was on Monday. I was prescribed Spironolactone- she said it stopped an androgen from converting estrogen to testosterone? Has anyone else with #PolycysticOvarianSyndrome been prescribed this?
    I’m trying to be as informed as possible for myself but I can’t find anything online that matches why I was prescribed it.

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    A year ago today - My #Flashbackfriday

    This was my Instagram post just a little bit ago. Thought I might share here for all my fellow warriors in case you need a bit of hope today.

    Here is my #fbf .

    —————

    The start of my journey after diagnosis came one year ago, thanks to many, including @malsawareness - Thank you. I can’t believe how much has happened since then. Diagnosis, diagnosis confirmation, trips to meet surgeon and have a block performed, (which for anyone reading, they asked if I was nauseous, and I said no, and then looked at my mom, and said, “*That’s* what nausea feels like? I feel nauseous 24/7.” I didn’t realize I was until I wasn’t. I also ate more and faster than usual and was seeing stars so much oxygen was getting to my brain.) and just a few short months later, surgery with that same doc. Recovery is still hard, and I am still trying to piece together what is improved from surgery, and what is other conditions. But about 6 months after surgery now, and I don’t regret it a bit. #NoFilter #nofilterneeded #forreasons #likeawesomeness #Flashbackfriday

    (And, yes, I use a lot of hashtags. A new one I should add, #hashimotos.)

    #chronicbadass #Fibromyalgia #fibrowarrior #posturalorthostatictachycardia #PosturalOrthostaticTachycardiaSyndrome #PCOS #PolycysticOvarianSyndrome #Hypothyroidism #ist #InappropriateSinusTachycardia #InvisibleIllness #InvisibleChronicIllness #ifight #iwin #BeBrave #Dysautonomia #autonomicnervoussystem #rosecea #Gastroparesis #ehlersdanlossyndrometype3 #MedianArcuateLigamentSyndrome #nutcrackersyndrome #IBS

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    I just want to say I love The Mighty! 💯💯💯

    I love The Mighty and get multiple newsletters from The Mighty sent to my email. I read at least an article or two every day. I feel so inspired by it it always brightens my mood and makes me feel like no matter what I CAN get through it and I'm not alone!
    #EhlersDanlosSyndrome #Bipolar #PolycysticOvarianSyndrome #TMJ #ObsessiveCompulsiveDisorder #PostTramaticStressDisorder #ComplexPTSD #Dysautonomia #HypothyroidismUnderactiveThyroidDisease #PosturalOrthostaticTachycardiaSyndrome #ThyroidDisease #Fibromyalgia #IrritableBowelSyndromeIBS #GeneralizedAnxietyDisorder #PanicDisorder #MyofascialPainSyndrome #EDS #HighCholesterol #SocialAnxiety #BipolarDisorder

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    This is Me

    Sea breeze in my hair as I ate fish and chips on the dock..... You’d never know this was my first “major” outing after spending just shy of a week in hospital for open surgery, and being discharged this past Wednesday. It’s the little things, like the baggy clothes I had to go out and buy because nothing I packed fits from the bloating post op. The hospital band and “allergy” band still on my wrist. The visitation sticker from visiting one of my “surgery buddies” who got bumped to this week instead of this past week. The anti nausea patch behind my ear. The meds in my system, and my mom’s phone going off that the pharmacy in her purse that was filled at discharge needs some dispensing. The little “Zipper Buddies” stuffed fox I got for me and my surgery buddies clutched tightly to my chest to hold my incision in case I cough or sneeze or laugh. This is the face of someone who is fighting. It’s a long recovery, but I have been blessed with magnificent doctors, and an amazing new set of friends going on the same journey, and we are figuring this out together. From walking the hallways hunched over in walkers in pain from the 5”-ish long incision, to standing straighter day by day, and trying to breathe through the pain, as we shuffle in our “fall risk” grippy socks. And this surgery only tackles one diagnosis. But I’m just gonna keep shufflin’ in my grippy socks that say “Slay” on the bottom, and live up to what they say. This is what rare looks like. This is what MALS looks like. This is what chronic illness looks like. This is what one semi good day looks like. This is what I look like. #filter #filterneeded #forreasons #likeawesomeness #mylightingsucks #ChronicIllness #chronicbadass #Fibromyalgia #fibrowarrior #POTS #posturalorthostatictachycardia #posturalorthostatictachycardiasyndro me #PCOS #PolycysticOvarianSyndrome #Hypothyroidism #ist #InappropriateSinusTachycardia #InvisibleIllness #InvisibleChronicIllness #ifight #iwin #BeBrave #Dysautonomia #autonomicnervoussystem #rosecea #Gastroparesis #ehlersdanlossyndrometype3 #MedianArcuateLigamentSyndrome #nutcrackersyndrome #IBS

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    Sick of PCOS

    I’m so sick of PCOS. I eat lightly and never lose weight. I don’t know what to do! #PolycysticOvarySyndrome #PolycysticOvarianSyndrome

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    How do I know if I should go to the doctor for a PCOS diagnosis?

    I have not been diagnosed with PCOS however my mom's sister has. I looked up the symptoms of PCOS on Google ( I know kinda dumb but it's my only resource) and I've had most of them. Most recently a pain in my pelvic area for about 4 days. It's usually not that bad but sometimes it's really uncomfortable. Help #PolycysticOvarySyndrome #PCOS #PolycysticOvarianSyndrome

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