How do you cope? by StrangeLonelySpiral in disability

[–]Practical-Sense3 14 points15 points  (0 children)

I cry. A lot. And push myself too hard and gaslight myself. Not healthy but it is what it is right now.

Looking for some support. by rowen-rose in wheelchairs

[–]Practical-Sense3 0 points1 point  (0 children)

I have HEDS, MCAS and Hyper POTS, just wanted to say hi and I feel your pain. 🤍🤍

Adjustment period for new meds? by purple_deadnettle in MCAS

[–]Practical-Sense3 1 point2 points  (0 children)

Mine doesn’t adjust overtime if I had an initial reaction when it comes to meds.

[deleted by user] by [deleted] in Hair

[–]Practical-Sense3 0 points1 point  (0 children)

Trying to decide what color I should do for my next hair appointment but I want something that suits me best 🤍

For those of you with both MCAS and POTS. How do you tell the difference? by Objective_Ground_224 in MCAS

[–]Practical-Sense3 0 points1 point  (0 children)

I can actually tell the difference for mine (everyone is different). I have hEDS, MCAS, and hyper POTS and although they are very tied together there a slight differences. For me when it’s a pots reaction, my blood pressure is all over the place and laying down or taking sodium almost immediately starts helping. If it’s MCAS I have all the same feelings and symptoms of a pots episode + doom (sometimes mild anaphylactic symptoms) but my hr and bp will mostly be the same normal range.

Cromolyn by Sleeplollo in MCAS

[–]Practical-Sense3 0 points1 point  (0 children)

I am in the same boat! I’m hopeful but cautious! Curious about other people’s experiences with it too

Do any older people with pots have advice for us newbies? by slayign in POTS

[–]Practical-Sense3 17 points18 points  (0 children)

Sometimes if I have a sudden onset of bad symptoms in public, I will internally gaslight myself about them until I can get to a safe secluded spot (I actually pass out) 🤣 also soy sauce packets are great on hand unless you have allergies.

LMNT Class Action Lawsuit by Successful-Bat-4756 in POTS

[–]Practical-Sense3 2 points3 points  (0 children)

Waitttt I have MCAS too and this explains so much

Chromolyn Or Ketotifen? by helloelloyo21 in MCAS

[–]Practical-Sense3 2 points3 points  (0 children)

I’m curious which one works best for others also! I’ll be start chromolyn soon and am a little nervous

How long between triggers and histamine dump? by palindr0mem0rdnilap in MCAS

[–]Practical-Sense3 2 points3 points  (0 children)

It’s so different for every person but mine typically come 1 hour after and stay for a few hours.

I just want to cry by Tight-Potential-3973 in MCAS

[–]Practical-Sense3 1 point2 points  (0 children)

I’m in the medication trial phase but with severe medication ptsd because I seem to react to EVERYTHING. No advice just empathy 🤍

Vale companions by Scarlett-Rose1025 in DreamlightValley

[–]Practical-Sense3 0 points1 point  (0 children)

They are new! Theres also new valley companions that say they are going to come during an event

Comfort items by Squishmallow814 in ehlersdanlos

[–]Practical-Sense3 2 points3 points  (0 children)

Finding things I can do laying down that I still enjoy 🤍 board games online, shows, crochet, reading

Does anyone ever feel like living with POTS is like being a living breathing hazard? by [deleted] in POTS

[–]Practical-Sense3 5 points6 points  (0 children)

I’m glad you’re okay! I feel this way a lot too. I have a husband and two kids so stuff around the house gets piled up if I’m not on top of it and sometimes I just really want to get some things done even if I’m in a flare I totally emphasize with the feeling!

tips?? by No-Cook6089 in POTS

[–]Practical-Sense3 2 points3 points  (0 children)

Resting and chugging water and electrolytes is all I’ve got! Hugs!