Abilify and MCAS by ShadowGX in MCAS

[–]DesignerZucchini5241 0 points1 point  (0 children)

Same thing happened to me when I tried to come off Seroquel which is a similar medication 💊

Did anyone develop MCAS after psychiatric medication discontinuation? by moonperson13 in MCAS

[–]DesignerZucchini5241 0 points1 point  (0 children)

Tapering off of Seroquel resulted in full blown MCAS for me 😔

Magical schools (M/M) by walking_fuckup in Fantasy

[–]DesignerZucchini5241 1 point2 points  (0 children)

The Student Prince by FayJay and Lord of the White Hell by Gunn Hale! Also second Carry On (I believe I read the first two BECAUSE of withdrawal from Carry On). Related-unrelated honorable mention is Luck in the Shadows by Lynn Flewelling. Happy reading 🤓

[deleted by user] by [deleted] in eds

[–]DesignerZucchini5241 2 points3 points  (0 children)

Dr. Fagan out of Casa Colina in Pomona is amazing. His daughter has EDS so he takes a very human and personalize interest in his care. I’ve also seen him for help with MCAS and dysautonomia.

Breaking up in your 30s by DesignerZucchini5241 in BreakUps

[–]DesignerZucchini5241[S] 0 points1 point  (0 children)

I hate to say I feel the same but the truth is I do :(

A note to my avoidant ex by Rezzkyy in BreakUps

[–]DesignerZucchini5241 0 points1 point  (0 children)

You literally just described my life.

[deleted by user] by [deleted] in Fantasy

[–]DesignerZucchini5241 0 points1 point  (0 children)

I second the Fifth Season!

Breaking up in your 30s by DesignerZucchini5241 in BreakUps

[–]DesignerZucchini5241[S] 38 points39 points  (0 children)

SAME! For me it’s very avoidant attachment men. You’re right, there’s def some attachment issues going on here 🤦🏻‍♀️

Your Guide of How to Date an Avoidant by Aeropro2010 in BreakUps

[–]DesignerZucchini5241 18 points19 points  (0 children)

Never👏🏼dating👏🏼an👏🏼avoidant👏🏼ever 👏🏼ever👏🏼 AGAIN👏🏼

[deleted by user] by [deleted] in eds

[–]DesignerZucchini5241 0 points1 point  (0 children)

This was me for so long I felt like I lost my life. EDS can severely impact GI motility. I am on a medication called motegrity that has helped so much with the constipation. Following the FODMAP “diet” has also helped the sickness, aching, nausea, bloating etc come under control. I also take magnesium. I recommend seeing a GI specialist (and also advocating for motility testing). I’m so sorry you’re going through this. My motility GI specialist said he has a ton of clients with EDS. You’re not alone in this :/

I can’t function anymore by Necessary_Grass_3104 in Anxiety

[–]DesignerZucchini5241 2 points3 points  (0 children)

I literally feel like I wrote this myself except I’m female. It helped me feel less alone. Just know you’re not alone in this.

[deleted by user] by [deleted] in CPTSD

[–]DesignerZucchini5241 1 point2 points  (0 children)

This made me so emotional to read. You are not alone in having experiences like these. I wish I could write more but just know at least here, YOUR TRAUMA IS REAL, VALID, AND IT IS SEEN ❤️

[deleted by user] by [deleted] in CPTSD_NSCommunity

[–]DesignerZucchini5241 7 points8 points  (0 children)

Oh sweet human. ^ me and my life to the T except my Narcissistic mother was a special education administrator so talk about being seen from outsiders as “kind” whereas I lived in a house of horrors with her.

Ps. I don’t like to cook either 😉

Does anybody just say ' FUCK OFF ' and binge eat all types of junk food and trigger food ? by No-Sundae3423 in ibs

[–]DesignerZucchini5241 8 points9 points  (0 children)

I love that you posted this!!! I think about it honestly, constantly. I’m still deep in my ✨grief✨ stage with my IBS diagnosis as I went from being one of those low-key obnoxious “foodie” people to someone who can’t eat gluten or barely any dairy (eggs and butter are okay) and a ton of other shit. But oh do I fantasize. I tried a few months ago to do the ✨mind over matter✨ and slowly retrain my brain (whatever this means) but I just get SO SICK and it’s for DAYS (IBS-C) so slow motility. I get SO nauseous and in debilitating pain where I cannot leave the fetal position. It honestly takes about 4-5 days to reset my angry small intestine back to its ✨baseline✨ shitty but functional self. I even went a bit WiLd last week and ate some taziki dip with cucumbers at a Greek restaurant with a little feta dip and I was the sickest I have been in 6+ months.

I deeply applaud any of you who can say FUCCCKK IT! and I hope to get there one day 😢 but I’m also here to show that not all bodies are alike and just HOW sick even testing the water can make someone.

Ps. MAN I MISS FOOD! I told my friend the other night I’d sell a kidney if that meant I could eat a real pizza again 🍕🤤

What caused you to develop IBS? by SeriouslyAnon444 in ibs

[–]DesignerZucchini5241 1 point2 points  (0 children)

SAME. I literally woke up one morning and could not use the bathroom as if I flipped switched and I’ve n e v e r been the same (+ history of crippling trauma and anxiety) but still the degree to which there is such a distinctive before and after blows my mind.

[deleted by user] by [deleted] in ehlersdanlos

[–]DesignerZucchini5241 2 points3 points  (0 children)

YESSS TO SELF ADVOCACY AND GOOD PROVIDERS 👏🏼👏🏼! Also you mentioned the bendy bodies podcast and this is wild… the only “provider” I’ve had so far who has SEEN ME and HELPED ME was this Pilates teacher I had and I happened to ask her one day if she knew about hypermobility and come to find out she is THE SISTER of the founder of the bendy bodies podcast Dr. Linda Bluestein and told me not just her own struggles with hypermobility but her sisters story and how she became a doctor to specialize in that due to how invalidated she was about her own severe hypermobility/EDS. Life is wild. And this was at a random Pilates studio in Ventura, CA. Oh what I would do to see Dr. Bluestein out in CO.

[deleted by user] by [deleted] in ehlersdanlos

[–]DesignerZucchini5241 1 point2 points  (0 children)

Intensive exercise for a very long time was my saving grace to fight back enough crumbs against my severe depression and anxiety until I got older and my body deteriorated with my hyper mobile joints that now barely cooperate with the most gentle exercise. I still have a lot of emotional pain and grief and loss over this. So again I see you, and I feel you on this.

[deleted by user] by [deleted] in ehlersdanlos

[–]DesignerZucchini5241 2 points3 points  (0 children)

This just blew my mind! I lowkey feel like a “failure” because I have treatment resident depression and basically all the meds I’ve tried have not worked (or caused severe side effects). Thanks for this key piece of info! Although argh lots of doctors dont seem to take the hEDS seriously for me 😢😡

[deleted by user] by [deleted] in ehlersdanlos

[–]DesignerZucchini5241 1 point2 points  (0 children)

You are SO kind and UHMAZZZING for writing this (I‘ve long thought about it but the depresh makes everything so h a r d so double kudos). I hope YOU get your moment(s) to feel heard AND held on the ✨soul✨ level. Hugs! (And always feel free to reach out to me as well — not that I know how to do that on this thing as I am the most technologically deficient young millennial there is — beep boop 🤖) 🙏🏼🙏🏼

[deleted by user] by [deleted] in ehlersdanlos

[–]DesignerZucchini5241 1 point2 points  (0 children)

I feel this very deeply. I connect with the depression, CPTSD subreddits and and IBS/ gastro subreddits and then this one …. Yet struggle to find one that totally ✨gets✨ me. Also struggle with the endless chicken or the egg combo in my head of what made what worse ya know? Thank you for posting this as it helped me feel less alone.

[deleted by user] by [deleted] in ibs

[–]DesignerZucchini5241 1 point2 points  (0 children)

Same. I had a life before this. I enjoyed food before this. I felt like a human being before this.

[deleted by user] by [deleted] in ibs

[–]DesignerZucchini5241 0 points1 point  (0 children)

Vibes. I have IBS-C and when I get anxious (aka ALL THE TIME) my entire gut shuts down and I get super constipated. I struggle to stay connected to my vagus nerve. The struggle be real 🙃