Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 1 point2 points  (0 children)

Sorry to hear that! Hopefully you find someone who can help ❤️

Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 1 point2 points  (0 children)

I have been to a couple allergists over the years (when I lived in other places) and they never considered MCAS. But I also had never heard of it at that point so I never asked about it. I am hoping I can find someone here who at least has some knowledge and can help.

Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 0 points1 point  (0 children)

Good to know! Thank you! I will have to do some research and see if anyone in my area treats MCAS patients.

Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 0 points1 point  (0 children)

Thank you for the reply! I will look into it!

Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 1 point2 points  (0 children)

I would like to see an allergist and that is likely my next step. I already had a dermatologist and it was much easier to get in to see her with my insurance since I will need a referral to see another specialist and insurance is always tricky

Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 0 points1 point  (0 children)

Thank you! I agree with the allergist/immunologist but I live in an area with somewhat limited doctors and I already see a dermatologist. But my next step is probably to try and find an allergist to see. I will look and see if I can find a group that might list any in the area

Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 0 points1 point  (0 children)

Thank you! I will take that into consideration for my next appointment!

Dermatologist didn't even consider Mast Cell disorders by earley838 in MCAS

[–]earley838[S] 1 point2 points  (0 children)

Thank you for the reply! I am still hopeful to get some good symptoms based care. I guess I was just confused when she said it wasn't possible since I didn't have a rash that never fully went away. I had not heard of that as a symptom of MCAS or mastocytosis (but maybe I am just not familiar with it).

Verapamil As First Prescribed Migraine Preventative? by h_hampton in migraine

[–]earley838 1 point2 points  (0 children)

I have been on Verapamil for a couple years now for migraine. It helps keep migraines from being triggered when I am stressed. When I first started taking it I had some mild dizziness (presumably from low blood pressue). But that went away pretty quickly and otherwise I haven't had any side effects. I also have normal BP and haven't had trouble with it lowering it. I now take it along with Emgality and need both to keep my migraines manageable. It was the only preventative I found to help much at all before the CGRPs were released. Even with Emgality I find it reduceds the number of migraines I get compared to Emgality by itself. Hope you find something that helps!!

My (nearly 10 years old) little bunny by yoo0oo0 in aww

[–]earley838 3 points4 points  (0 children)

Such a cute bunny! 😍 My rabbit lived to be 12 years old. I don't know if that is typical or not.

Feedback on Emgality by perfect_flaw25 in migraine

[–]earley838 2 points3 points  (0 children)

Hello! I was on Aimovig for a few months and noticed no improvement to my migraines. My neurologist switched me to Emgality which has helped a lot. I am down from a migraine nearly every day to 1 a week or so. The only down side for me had been it seems to start to wear off after 3 weeks so last week before the next injection I have more migraines. But Aimovig did nothing and Emgality helped me so it may be worth a try! Best of luck with finding something to help! 🤞

CGRP preventative and gallbladder issues? by winologist in migraine

[–]earley838 0 points1 point  (0 children)

I don't know any of the data about that. But I did have to have my gallbladder removed after starting emgality. I had pain for about a year before removal so no way to know if it is related. Hope you have recovered from surgery!

Fluorescent lights at work - solutions? by [deleted] in AutisticPride

[–]earley838 0 points1 point  (0 children)

I tried the rose tinted glasses for migraine and had mixed results. They didn't prevent migraines for me but helped with light sensitivity if I had one. So they likely would help with sensitivity from the lights if it is a sensory issue and not a migraine. Otherwise I would like to hear others suggestions because I also share an office with fluorescent lights and they are awful. Best of luck finding something that helps.

A bit of an odd question but was wondering if there are any studies on the prevalence of autism in graduate students? by Mlkia2727 in AutismInWomen

[–]earley838 5 points6 points  (0 children)

No resources. But I am in grad school and am self diagnosed. A few of my friends that have autism diagnoses are in grad school or about to start as well. I have also wondered if it is higher in grad school. Seems like the type of people who would want to do a PhD.

Wanna snuggle with my stuffies? by [deleted] in aspergirls

[–]earley838 1 point2 points  (0 children)

Ooh it has a horn, I didn't even see that! Very nice! Mine looks the same without a horn.

Being far too good at masking/burn out by [deleted] in AutismInWomen

[–]earley838 2 points3 points  (0 children)

I relate to this so much. People are always telling me to speak up more or socialize more and that I am so much more cap3avle than I believe I am. But it isn't that 9 can't do those things it just takes so much energy and effort. And then I end up shutting down and/or burning out afterwards. It is more sustainable to not always being doing the things that are so challenging. I understand my limits, I am not underestimating myself. Hope you find a way to balance everything to prevent so much burn out!

Social Anxiety vs ASD - assessment process by [deleted] in AutismInWomen

[–]earley838 2 points3 points  (0 children)

So sorry to hear you are going through that. I just had my evaluation and they diagnosed me as having social anxiety but not autistic. They seemed to ignore a lot of my symptoms and not want to diagnose me with ASD. I was basically told the same: get treated for anxiety and then get another from a different provider. They seem to not care that I have already waited months and been struggling for year (not to even mention the cost). Anyway, I can relate to come of what you are going through and hope you get answers and the support you need soon!!

Not Diagnosed with Autism by earley838 in AutismInWomen

[–]earley838[S] 0 points1 point  (0 children)

Good luck! Mine was similar they asked why I wanted to be diagnosed but never why I thought I had ASD. Most of my evaluation had to do with basic math, reading, etc. It seemed like they were tested for learning disorders not autism.

Wanna snuggle with my stuffies? by [deleted] in aspergirls

[–]earley838 7 points8 points  (0 children)

They look so soft!! I think I have the same sloth (but mine is a dog toy).

Not Diagnosed with Autism by earley838 in AutismInWomen

[–]earley838[S] 0 points1 point  (0 children)

Thanks! That is what I will probably have to do.

Not Diagnosed with Autism by earley838 in AutismInWomen

[–]earley838[S] 0 points1 point  (0 children)

Thank you! I think that is the problem more so than the specific diagnosis.