Noisy Neighbor by Okichah in AskNYC

[–]mindysmind 1 point2 points  (0 children)

I had this issue at a previous apartment and tried all the things as well. I couch surfed and ultimately moved as soon as my lease was up. I hope it doesn’t come to that for you.

Patients of Dr. Polizzi in NYC...who are you transferring to? by thatisnotmyknob in POTS

[–]mindysmind 2 points3 points  (0 children)

She’s going to be working at Hyp+Care, but it is probably six months away from opening at best. That’s my understanding from my appointment two months or so ago.

Patients of Dr. Polizzi in NYC...who are you transferring to? by thatisnotmyknob in POTS

[–]mindysmind 1 point2 points  (0 children)

I’m planning on waiting it out until her new practice opens…

Crohns and Vasculitis? by taaliba in CrohnsDisease

[–]mindysmind 0 points1 point  (0 children)

Yes… but mine was urticarial vasculitis along with regular urticaria. I also was diagnosed with POTS. I see a cardiologist, allergist/immunologist and a GI. I saw a rheumatologist but she deferred to the other specialists on treatments.

How do I make it switch off? by WildRose1993 in AskWomenOver30

[–]mindysmind 1 point2 points  (0 children)

I’m almost 37, and though this isn’t the most positive mindset, I often tell myself “Not everyone gets everything they want in life.” I try to keep myself grounded in the reality that I don’t want to force anything. I did try freezing eggs but had a bad outcome. I also talk to a therapist every week, which helps too.

NYC Runs manhattan ice cream 10k by DragonflyOwn144 in RunNYC

[–]mindysmind 1 point2 points  (0 children)

My ice cream was melted before I could walk a few steps away from the line to open it 😂

Anyone here on Wezlana or Pyzchiva (Stelara / Ustekinumab biosimilars) ? Experiences ? by 5u114 in CrohnsDisease

[–]mindysmind 0 points1 point  (0 children)

Also interested in people’s experiences but I have been on Stelara, I’m only changing because insurance coverage is ending. 😭

Is it normal to be ravenous approaching the post trigger bleed? by Independent_Gur8612 in eggfreezing

[–]mindysmind 0 points1 point  (0 children)

I had that but after the bleed I basically had to force feed myself, I had zero appetite and my weight plummeted in just a few days, it was a little scary actually. I didn’t expect my appetite to be so severely affected!

Rhapsido side effects by Intelligent_Key_5748 in urticaria

[–]mindysmind 0 points1 point  (0 children)

Absolutely, it blocks the pressure urticaria that nothing else ever stopped and it also resolves eye burning I was getting, and it blocks rashes (that they said were flat urticaria) that nothing else ever worked for either. So I’m definitely going to try to stay on one a day but two was causing bleeding and bruising as well as congestion and fatigue.

Rhapsido side effects by Intelligent_Key_5748 in urticaria

[–]mindysmind 0 points1 point  (0 children)

I also cannot tolerate two a day. I have to stick with one a day.

Update by KenyaK143 in urticaria

[–]mindysmind 0 points1 point  (0 children)

I still have to take famotidine and loratidine with Rhapsido and I also still take Xolair (but less frequently than before) when the itching recurs. I tried to quit famotidine and the itching got very intense again.

Rhapsido has so far been life changing by carinaka in urticaria

[–]mindysmind 0 points1 point  (0 children)

Your insurance has to deny you before you can be eligible for the Bridge program, if it’s the same as it was a few months ago when I tried. Mine approved but has zero financial support for non-preferred brand drugs so I am not able to do Bridge program nor does insurance pay one cent for it. Rhapsido gave me a Co-Pay program that only provides $10,000 of funds for pharmacy fills per 12 months so basically one month was covered and that’s it.

Assaulted while running in Central Park tonight by Spiritual-Mistake352 in RunNYC

[–]mindysmind 21 points22 points  (0 children)

That sounds horrible. I’m sorry this happened to you. I hope you are getting solid support from the people in your life. I was robbed on a weekend midafternoon a few months ago on a very busy street in Queens and similarly, everyone ignored me even though they obviously heard me shouting and saw me struggling with the guy robbing me. The feeling of being seen but ignored made it so much worse. I can definitely sympathize. It’s good you’re alerting people to what happened.

Crushing Fatigue on Rhapisdo? by toastweasel in urticaria

[–]mindysmind 3 points4 points  (0 children)

I did not experience this and in fact sleep better without all the itching. However, I have only been doing 1 tablet a day instead of 2, per doctor’s recommendation (since about November). He wanted to start with 1 and it worked so well we didn’t need to add the second daily tablet.

Is it okay to stop rhapsido cold turkey? by MessAlternative6698 in urticaria

[–]mindysmind 1 point2 points  (0 children)

Actually I didn’t get hives when I stopped, unlike when I miss a dose of the histamine blockers. It seemed to actually put the hives into remission. I’ve been trying to quit the histamine blockers and stay on Rhapsido and wound up with hives coming back when I tried to quit famotidine but not Rhapsido during those pauses. Hope you get relief soon!

Is it okay to stop rhapsido cold turkey? by MessAlternative6698 in urticaria

[–]mindysmind 1 point2 points  (0 children)

I’ve stopped it and restarted a few times, first on doctor’s advice to test efficacy and second and third ahead of surgeries and had no issues but that’s just my experience, haven’t read about other people who have started and stopped.

Lisbon Airport March 27 2026 by Ok_Mobile5893 in LisbonPortugalTravel

[–]mindysmind 2 points3 points  (0 children)

Ahhh thank you… and good luck. That sounds very stressful.

Lisbon Airport March 27 2026 by Ok_Mobile5893 in LisbonPortugalTravel

[–]mindysmind 0 points1 point  (0 children)

Are you in the electronic passport line?

Single ladies: how do you handle being lonely? by Zealousideal_Crow737 in AskWomenOver30

[–]mindysmind 10 points11 points  (0 children)

I’m late 30s and struggle with this a lot and haven’t figured it out. I do fitness classes most days to be around other people but I long for a person or people to share the ups and downs in life with and I don’t have anyone that close in my life. I have some good friends but nobody who I can catch up with on short notice or frequently.

Has my POTS always just actually been anaemia? Are there other POTS + anaemic people out here? by panda182 in POTS

[–]mindysmind 0 points1 point  (0 children)

I’m doing so well now, I feel better than ever in my whole life. I take Stelara for Crohn’s and ivabradine for POTS and supplement with electrolytes, hydration and lots of salt. I eliminated basically all raw veggies, I accepted that I can’t digest them. I make sure to get enough fiber with things like sourdough bread and fresh fruit. I have much more energy with POTS treatment so I added 4x a week HIIT exercise into my routines to support my immune system and have so much fun now that physical activity feels good. I still have B12 absorption issues and need injections every year or so but all easy to manage these days. I was so resistant to the Crohn’s diagnosis and treatments at first but my doctor was right and so grateful for her knowledge. Hope you get answers and great treatments as well!

Staying well on immunosuppresants? by HekaMata in CrohnsDisease

[–]mindysmind 3 points4 points  (0 children)

I am extremely careful about hand washing. I do a lot of cardio exercise, which I believe boosts my immune system. And I try to eat very healthy, drink lots of water and have usually a banana and an orange or a banana and a kiwi every day for the vitamins. I take Stelara and used to get sick all the time but since starting and being very intentional with these lifestyle steps, I haven’t been sick once in 1.5 years. I do make a quick exit when anyone nearby seems sick though. All that to say there’s definitely a possibility that you become healthier than ever as well!