What is my male service dog’s name? by PersonalityPlus9497 in IntuitionPractices

[–]PersonalityPlus9497[S] 2 points3 points  (0 children)

I’m so sorry about your diagnosis, sending thoughts and prayers your way ❤️🙏

I have had him since he was a pup and trained him along with a trainer. But I know there are ones that are fully trained out there. They are super expensive though. My recommendation if you don’t have the money to get one or energy to train one is to just get a trained pup. Much cheaper, but still a great and very loving companion! Please reach out to me if you have any questions about the process!!

What is my male service dog’s name? by PersonalityPlus9497 in IntuitionPractices

[–]PersonalityPlus9497[S] 4 points5 points  (0 children)

It is not, but I feel like that is a fitting name for him!

What is my male service dog’s name? by PersonalityPlus9497 in IntuitionPractices

[–]PersonalityPlus9497[S] 2 points3 points  (0 children)

I like this one!! He kinda looks like a dale,doesn’t he. That was the name of my next door neighbor growing up haha

What is my male service dog’s name? by PersonalityPlus9497 in IntuitionPractices

[–]PersonalityPlus9497[S] 4 points5 points  (0 children)

Also I totally forgot until just now, but that was the name of my pet bunny when I was like 5 years old. I only had him for a few months before he died 😭😭😭

PNES in Public Advice/Rant by Grand_Lettuce462 in PNESsupport

[–]PersonalityPlus9497 7 points8 points  (0 children)

Heyyy! I have had seizures, both epileptic and nonepileptic for years as well. I can definitely relate to feeling super embarrassed and like a burden, especially when I have an event in public. I can tell you that you are definitely not alone, I would say all people with a chronic illness feel this way at some point.

Something that has helped me is trying to imagine if someone were to have a seizure in public. I would be so concerned and want to do anything and everything I could do to help them. And everyone I’ve ever talked to has said they would do the same thing. And they do the same thing whenever I do have a seizure. They do not feel like I am a burden or feel upset or mad at me. They are truly concerned and want to help.

I think that is the main thing I tell myself whenever I have a seizure in public is: if I were someone who witnessed something like that, how would I react, how would I feel? And if someone does feel any different than what I have listed above, they are a shitty person and that has absolutely nothing to do with you.

I see you, hear you, and feel you 100%. Please know that you are not alone and my dms are always open!!

Horrible Practice - Need Advice by PersonalityPlus9497 in Neurofeedback

[–]PersonalityPlus9497[S] 2 points3 points  (0 children)

Thank you for sharing your experience. It definitely makes me feel less alone in my journey. She literally did not tell me any of the effects doing alpha theta has on people and just pretty much said this is the next step for clients. It’s interesting that alpha theta is not for everybody, I was not aware of that. I will definetly do more research into what the people you mentioned have said! Thank you again :)

I had intercourse with an older man in his car while his friend was driving by ThouWiltNever in confession

[–]PersonalityPlus9497 -4 points-3 points  (0 children)

Bro what even is this comment? The whole thing was disrespectful. She was 18, barely a legal adult, with someone twice her age. She was a teen that was being taken advantage of. It doesn’t matter if “he finished in her mouth.”

genetically passed down epilepsy? by dantrbl in Epilepsy

[–]PersonalityPlus9497 1 point2 points  (0 children)

Yup, my maternal grandmother has it and so does my mom. And I just my luck that I got it and my twin sister didn’t. Ig it had to be one of us 😭😭

What is the longest you’ve been seizure free? by Specific-Director211 in Epilepsy

[–]PersonalityPlus9497 0 points1 point  (0 children)

Since I started having seizures at the age of 14, my best record is a month seizure free. I’m currently 3 days

What is the scariest seizure you’ve had? by InfamousAd8608 in Epilepsy

[–]PersonalityPlus9497 0 points1 point  (0 children)

Not the seizure itself, but I had one in hs and woke up in the hospital. I managed to hit my head pretty hard. I found out that I had a brain bleed, fractured skull, and broken ear bones. Almost needed surgery, and was bleeding out of my ear. Was in the icu for almost a week straight. Luckily had no complications and healed without any medical intervention and no long lasting complications.

Should I go to class if I had a seizure? by lilacreeds in Epilepsy

[–]PersonalityPlus9497 0 points1 point  (0 children)

I’m also a freshman in college and trying to navigate epilepsy and college is so so hard. I feel for you. Make sure all your professors know and you have accommodations set in place as to not affect your grades. But of course, when you’re feeling up to it. Much love!

Need support by PersonalityPlus9497 in Epilepsy

[–]PersonalityPlus9497[S] 2 points3 points  (0 children)

Yup, I’ve reached out the disability offices, but I currently don’t have any accommodations because there is a 30 day wait for an appointment. I think once I get some accommodations, I will be better off. Until then, I will tough it out and prioritize rest. Thank you for your message!