DallasMiranda
Region: US
Thursday 09 July 2026 23:50:00 GMT
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ManderAlden :
Do you have a P.O Box we can send cards to Tati while she is away?
2026-07-10 03:43:39
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jeanna :
so glad she has a new doctor that is more attentive to her needs!! sending all the good vibes y’all’s way ❤️❤️
2026-07-09 23:58:19
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ireadthemanual :
My dad has a neuropace stimulator implanted into his brain under his skull for his seizures. It has helped SO much. They didn’t go away but they have significantly reduced them. He was part of a research study so he was one of the first few people to get it
2026-07-10 00:59:27
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Bbybrie27 :
I don’t blame her for being scared. This procedure is extremely scary. I will keep you guys in my prayers and Tati is extremely strong and will get thru this and you will too. I send nothing but love and support
2026-07-10 00:15:26
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morenita28 :
My brother went through that. The results are worth it. They are quick to respond to when they get seizures
2026-07-10 00:02:28
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Roe :
make it like a fun girls adventure with her.. get matching pj's for each day, do self care things face masks small things like that or games, do stuff that she likes and with gma at night certain snacks or movie themed snacks n have movie type nights n in the meantime plan it with her so it doesnt stress her so much plus it'll help from being so bored between procedures just sitting in a bed
2026-07-10 19:59:22
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Minikin Petz LPS :
Hang in there queens❤️
2026-07-09 23:56:59
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jess :
Its very stressful but if they can figure it out and do something this can be a tiny blimp that leads to an even better quality of life for her. I hope it works out.
2026-07-10 00:12:35
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TinaJ :
my daughter has pcdh19 epilepsy. nobody understands. the medicine is so hard on the liver. my thoughts are with you both
2026-07-10 00:05:51
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Allison :
I have epilepsy & also go for EEG monitoring once a year. I’m on Keppra & it’s been the best med I’ve been on. I’m 45 & got diagnosed @2. Hope it goes well!
2026-07-10 00:56:56
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pepitabonita :
Aww, Tati 🥺 I hope all goes well Dallas ❤️🩹
2026-07-09 23:56:49
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falilatu(fa-lee-la-t :
I’m a neuro nurse in an Neurology/Neurosurgery/Epilepsy monitoring unit! Because Tati’s events are so frequent, I imagine they will capture what the need fairly quickly! Hopefully she’s only there for 4-5 days. Sending you so much love 🫶🏿
2026-07-10 04:04:32
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Carluch :
sending hugs to your family 🙏🏼❤️
2026-07-09 23:53:33
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Stephanie Christine :
I had this study about 10 years ago. I only ended up staying for 24 hours and they told me I could go home. It depends on the hospital and the individual but if they see what they need to see within a shorter timeframe they can let her go home within a shorter timeframe! You can also contact the hospital prior to her stay and see if someone (yourself, gma, etc.) can stay with her overnight since she has a developmental/mental disability. EMU’s (Epilepsy Monitoring Units) are typically accommodating!
2026-07-10 00:52:18
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Maddy☀️🌊💗 :
I hope her hospital visit goes well! 💗
2026-07-10 00:10:07
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Gypsy Soul :
You’re an AMAZING sister
2026-07-10 01:08:47
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meatballstewenthusiast :
i hope this is helpful for you guys y’all deserve to have answers i’m glad y’all found a doctor willing to do more for her ❤️
2026-07-10 00:31:12
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☆mwah :
ur such a good sister always continuing to do the most for her! yall are so blessed to have each other
2026-07-10 04:12:11
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R A C H E L 🌻 :
I’m glad you went and talked and hopefully now everyone is on the same page and can’t help her as well 🫶
2026-07-10 00:24:08
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Hbro23 :
Poor Tati I hope everything goes good and the stay doesn't feel long for her🫶🏻
2026-07-10 01:17:52
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Laura{ₘₐₘₐ} :
Oh sweet girl. Everything will be okay.
2026-07-10 00:34:29
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Temp :
That is a big scary transition I will keep Tati and you guys in my prayers … I have a special needs daughter with a brain condition and you definitely teach me a lot with your openness thank you ❤️🙏 🥰
2026-07-10 00:10:20
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Alyssa Klaczynski :
Tati got this! I’ve done the stay and yes it’s hard but it’s worth it. Tati is a strong young women!
2026-07-10 00:14:31
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LauraLou22 :
My daughter got the VNS in 2012 when she was 5, it was the absolute best decision ever. Shes off all seizure medications (she would have up to 30 seizures some days). If you need someone to talk to about anything let me know ❤️
2026-07-10 02:42:51
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