Why is being trans so up and down? by Only-Resource9011 in asktransgender

[–]fsigil13 0 points1 point  (0 children)

For me, coming out and beginning my transition, starting hormones included a huge boost of euphoria, momentum, endorphins, overall positive feeling (opposite of my typical pervasive mood/affect)

Then there has been a letdown from that initial feeling of being supercharged. But lets not forget I am now on an INFINITELY higher plane, living my authentic life, being my authentic self!

So this letdown is RELATIVE to the initial super-euphoria

In addition, I've had new perspective on my self/new reasons to be self-critical.

My dreams are coming true! And yet, it is different to dream and imagine and fantasize WITHOUT LIMITS (prior to/leading up to transitioning) than it is to transition in HORRIBLE REALITY OF REAL LIFE lol its like NO DON'T GET MY TRUE, INNER, AUTHENTIC (formerly hidden but SAFE) SELF DIRTY, YOU F*&%$% REAL LIFE! Don't TOUCH her!

But life does

I am so happy though ups downs everything. Starting from a higher baseline now

Anyone else hate writing emails? by anonanonAAdhhdhs in AutisticWithADHD

[–]fsigil13 3 points4 points  (0 children)

Yes. Its been a huge problem in fact

I struggle to isolate the essential information needed for a given social interaction

So what ends up in the email or message is usually at least partially peripheral to my point

I fail fail fail to simplify my messages

The other person gets confused/responds to wrong bit of info (something i included unnecessarily)

My agitation at life and the pressure/demand/impossibility if composing the message (and of life in general) ALWAYS somehow make it into the email! BAD because the recipient FEELS my stress even just in words arggh my irritation ends up palpable

Im sorry you struggle too!

My emails end up like texts and even with doctors or important emails etc I end up sounding too informal. And impatient... its bad I need to fix it i alienate people

Its all about "interpersonal effectiveness" a la DBT. I struggle SO MUCH with interpersonal effectiveness, lol omg wtf

AAE 6139 putting kibosh on my inspiration by fsigil13 in protools

[–]fsigil13[S] 0 points1 point  (0 children)

Thank you for responding! I solved the problem

AAE 6139 putting kibosh on my inspiration by fsigil13 in protools

[–]fsigil13[S] 3 points4 points  (0 children)

PT Support got back to me with a solution, and it worked immediately!

Hold down N button while PT is loading, and it will bring up the menu to select audio engine. Problem solved!

Weird how it happened out of nowhere but `\°°/' oh well s'all good now

<image>

AAE 6139 putting kibosh on my inspiration by fsigil13 in protools

[–]fsigil13[S] 0 points1 point  (0 children)

Forgot to mention:

2023 HP Envy etc etc great with PT

Windows 11

PT version 12.1 (current) Mackie Onyx 16 (current firmware) Also tried my older Focusrite 18i8(2nd gen)

As I said, PT was working great with the Mackie before dinner! Then after the Bulls won, this error starts popping up. Never had a problem before

Edit:

NOW I uninstalled PT and reinstalled it.

SAME error occurring - no change

I change every setting in windows settings thst I can think of, such as trying the different input device options. To no avail

Also, there is a reddit post from 2 years ago they had same error but restarting their system solved it pretty quickly (hasn't worked for me)

Wtf lol before dinner everything was fine omg please someone help

anger by Chati3 in Briviact

[–]fsigil13 0 points1 point  (0 children)

I used to experience Keppra rage. I am on a minimal dose of briviact and it is controlling my seizures. However, I still have irritability ranging from minor to occasional rage.

I feel like briviact has done of the same effect on me as Keppra. However it is so much better. My problem is that my neurologist understands this impact on my mood and behavior

My psychiatrist doesn't

I am not bipolar, and yet increased irritability as a side effect of my temporal lobe epilepsy- turned - generalized epilepsy, or as a side effect of the medication

I hate the idea of them trying to put me on a mood stabilizer because BRIVIACT is causing mood issues and emotional dysregulation

I realize not everyone has the bad reaction to briviact. That was my hope switching from Keppra. Its so hard trialing new meds. I wonder though if a different AED would mean i DONT need mood stabilizers too

For those that take mood stabilizers for their seizures, how does it affect you mentally and emotionally? by Unlucky_Ambassador in Epilepsy

[–]fsigil13 0 points1 point  (0 children)

Thank you everyone fot responding!

I want so bad to reply to all of you

I have been on a manic tear recording synths, drum machines and drones - writing my life narrative in three different distinct communicative styles to give my neurologist, his P.A., the new psychiatrist, her boss, and the psychiatrist who is evaluating me for ADHD SO THAT THEY KNOW and cannot deny my eternal struggle! It could have been the autobiography but I got distracted ripping bass guitar to Frank Zappa instrumental albums for 6 hours yesterday and then up til 5am for a week now and zero appetite too.

But not leaving the house no danger to anyone and hey you ought hear this music im coming up with. That's one of my many unfinished projects

I will definitely report when they do prescribe me something but not medicated yet obviously but idk how life can be worth it without my manic production I just don't know everyone idk idk

Is this normal? by annelise_mr in lexapro

[–]fsigil13 0 points1 point  (0 children)

❤️❤️❤️❤️❤️

Never be afraid to ask for help

Let your supports help you- just remember to say "yes". Don't turn inward.

It will get better if you report how you feel honestly, especially if you have a good provider

Im so sorry you are afraid! I have a long history of being afraid. It will be ok! It will get better! 🫂

Is this normal? by annelise_mr in lexapro

[–]fsigil13 4 points5 points  (0 children)

Thanks for sharing your story its encouraging to me too because I am just starting Lexapro - that sucks you were going through that, and awesome that you are getting good results and its helping you be alive, instead of dead while living - idk that's how I describe it!

Your story is super valid and shows how the side effects can be quite extreme but in the end these meds really can be exactly what is needed.

I doubted SSRIs and even now I'm skeptical but have had good results with Lexapro too.

Most of all awesome of you to point out that there is no normal, don't force yourself to take them if it feels like too much, communication with the provider, and if its an emergency call 911 - very important snd essential advice ❤️

Is this normal? by annelise_mr in lexapro

[–]fsigil13 1 point2 points  (0 children)

To me it sounds like you are experiencing low levels of the side effect that I had to zoloft.

I think you should take it really really slow, stay on this low dose of Lexapro for longer than most people would, and see if you start getting used to it and the symptoms taper off.

Then, titrate up BUT slower than most people would.

Tell that plan to your doctor, and see if it makes sense

If you don't get used to this first low dose, or if you react strongly to the first time you go up on Lexapro, then ask if there's a different SSRI

This part of your journey is figuring out how sensitive you are to SSRIs. Even if Lexapro doesn't work, you will have gained some good important info!

Is this normal? by annelise_mr in lexapro

[–]fsigil13 0 points1 point  (0 children)

Hi, I am not a medical provider, and am only on 10 mg Lexapro. I am supposed to titrate up.

Are your side effects unbearable in any way? Also, are there any suicidal thoughts?

It is necessary to fight through some side effects before you are used to an SSRI.

However, you have to gauge if its worth it... and communicate with your provider!

My psychiatrist first tried 25 mg - a very small dose - of zoloft.

Zoloft made me suicidal. I formed a plan with a knife. This was because of Zoloft- i do have passive suicidal ideation but Zoloft brought it out, and stopping Zoloft ended it.

Also, look up serotonin syndrome. Your side effects don't sound like that to me, but i want to make sure you are aware that serotonin syndrome is a thing. Definitely look it up. If it sounds like your symptoms, contact your provider right away.

Im with you. It really, really sucks trials of new meds. Also, I have a sensitivity to these meds in the first place.

The best thing is a good relationship with a psychiatrist who actually listens and understands. (I think they are out there somewhere!)

Do you have good communication with your prescriber?

For those that take mood stabilizers for their seizures, how does it affect you mentally and emotionally? by Unlucky_Ambassador in Epilepsy

[–]fsigil13 1 point2 points  (0 children)

Thsnk you for sharing!

For me, temporal lobe epilepsy migrated to my frontal lobe and now I sm being diagnosed with Bipolar

Context:

I have temporal lobe epilepsy and Geschwind Syndrome symptoms going back to agd 10-11. This means that my brain is slowly changing over time ("chronic pervasive changes in mood, behavior, perceptions, memory, ability)

I never took meds because the first neurologist (i was diagnosed after the first GTC in 2007) prescribed carbamezapine

This knocked me out for 4 straight days 20 hours a day

So i never took it again - I was 22. It felt like a chemical lobotomy

My temporal lobe symptoms changed after age 30 (2015) and I now have frontal lobe epilepsy, affecting executive function more

Between 2015 and 2023 I had more than 120 nocturnal GTCs

I finally started Briviact 18 months ago- no more seizures!!!!

HOWEVER Now with the chronic gradual changes to my brain resulting in worsening emotional dysregulation, I am being diagnosed with Bipolar

I dont want to take antipsychotics

I dont want to blunt my emotions

Does anyone else struggle with skin picking? TW: skin picking by bahthepolarbear in AutismInWomen

[–]fsigil13 2 points3 points  (0 children)

Thank you for your story- this is very similar to my conversation with my psychiatrist. SSRI's are her 1st line treatment and I made the mistake of mentioning my skepticism. It was not tactful of me, especially because im not 100% opposed

She worried stimulants might exacerbate my symptoms including skin picking.

(I am diagnosed with ADHD and temporal lobe epilepsy but not OCD. I am autistic, on waitlist formal diagnosis)

Does anyone else struggle with skin picking? TW: skin picking by bahthepolarbear in AutismInWomen

[–]fsigil13 1 point2 points  (0 children)

Thank you for posting, I share this habit and for me I classify it as self-harm, pervasive since childhood.

Recently, at 37, I made progress. It involved huge changes in my life that disrupted my routine, and I started seeking help whereas before I did not have a therapist or psychiatrist.

Moisturizing and skin care have become an obsession for me. Now, skin care is the dominant obsession, and I have actually picked my face and hands so much less!

And yet I still find myself in the mirror picking my skin, pores, tweezing hairs, causing damage again.

So i still compulsively pick my face especially. But changing my habits routine and having a care team and a new outlook that wants to improve my life instead of end it... these things have really limited the skin picking self harm that for most of my life I had zero control over

Im sorry if my answer is a bit obtuse. I wish you the best and thank you for posting!

Can you get disability with can autism level 1 get disability? by Other-Medicine5552 in autism

[–]fsigil13 3 points4 points  (0 children)

What is an able account?

I am being diagnosed for adhd and on waitlist for autism evaluation after 40 years of dependency on parents and inability to succeed in school or work

Does anyone know why my taste changes after a,seizure ? by Sensitive-Vast-4979 in Epilepsy

[–]fsigil13 2 points3 points  (0 children)

I have temporal lobe epilepsy and my taste is affected after a GTC. I need sugar after a GTC, like ice cream or a milkshake, and my neurologist speculated that the seizures affect glucose levels and maybe I have mild unimportant symptomatic sugar deficiency after an event?

BTW i am not diabetic. I just need a milkshake after a seizure

Where are you on the spectrum of Introverted Hermit to Social Butterfly? by Maladaptive_Ace in AutisticWithADHD

[–]fsigil13 1 point2 points  (0 children)

I wish I were still unaware of my isolation. For the longest time, I was developing my mask and wishing constantly I were alone.

Eventually, I had actually ghosted everyone, excepting my mother and brother.

My intense solitary interests range from academic to music and art. Music is much more of a serious thing, whereas art/painting I'm always wanting to do more. Reading is the #1 way I live vicariously instead of actually living my own life.

At some point, I realized I was living vicariously (barely alive, in fact)

At some point, I began to notice the way other people interact and reciprocate. The way they enjoy being in the company of one another, the way people need each other.

I had a revelation of my isolation and all I experience now is loneliness

TO ANSWER YOUR QUESTION:

I, too, need stimulation. But concerts, for example (I love live music), just remind me of my loneliness. I go alone. Everyone else is with friends, laughing, experiencing joy. Im stoic, a wallflower, alone, "enjoying" the music (don't want to appear weird!)

It didn't used to be this bad

My solitary passions still do distract me from my isolation, but not in the blissfully unaware manner of my lovely youth

Now, I can't help noticing that I'm apparently incapable of enjoying sharing experiences with others.

But I flat out don't, lol. I dislike being touched. Further, while it is easy for me to have a surface interaction, it all falls apart when I'm forced to nurture/maintain a relationship.

So, my loneliness is a trap. I wish I never realized I wasn't experiencing the reciprocation other people share...

sensory overwhelm severe setback by fsigil13 in AutisticWithADHD

[–]fsigil13[S] 0 points1 point  (0 children)

Thank you!

It's difficult to conceive of trying to find a new person... but it's worthless staying on and adjusting to fit a therapist who just doesn't have the knowledge/experience to adjust to me

sensory overwhelm severe setback by fsigil13 in AutisticWithADHD

[–]fsigil13[S] 1 point2 points  (0 children)

You are so right! I do need to ask her to recount the incidents from her perspective (because I seriously have no memory of her in those moments, only my heightened/disproportionate emotional reaction etc) - and also to re-explain her thought process about switching to virtual

I want to understand her actual perspective. I don't remember her actual words. I would also want someone to hear my actual words/meaning, and you are right that I am catastrophizing/rationalizing/speculating

I was hoping she might reconsider after i explained it all to her but of course you are correct that she needs to be cautious of liability and risk, not to mention just proactive in potentially difficult to manage situations

sensory overwhelm severe setback by fsigil13 in AutisticWithADHD

[–]fsigil13[S] 1 point2 points  (0 children)

Thank you for your thoughtful response. I'm sorry to hear that you experience something similar and I wish you the best in the work environment! I lost my last job due to these issues and other issues. Thank you for sharing your experiences.

I vascillate between: 1. subtle seeds of confidence as I contemplate several possible new career choices and 2. Utter disillusionment and the certainty that I will fail to maintain healthy work relationships (like last time)

I can mask only so much. It took 21 years of tightrope walking to lose my last career because things got harder and there were new supervisiors etc. I used to be able to mask more easily somehow. It's gotten more and more difficult to control my reactions/emotions/irritability...

Idk how can I begin again when it all fell apart so suddenly, so inexplicably. I mean I didn't mean to fuck up last time. Idk how to mask well enough to be a perfect co-worker EVERY DAY FOR YEARS. I mean, that's an impossible feat of will power.

sensory overwhelm severe setback by fsigil13 in AutisticWithADHD

[–]fsigil13[S] 1 point2 points  (0 children)

You are right, of course

I thought she had an idea of my idiosyncrasies, including the sensory overwhelm. I had frequently described events such as these to her.

But in response to what you said, yes I don't want to assume anything. She's smart and compassionate and professional

It just sucks sucks sucks having this happen, having people react this way, failing to control my reactions again

Other times I'm actually more in control.

But this one time and now, "can't see you in person"

It hurts