▲ 51 r/galaxyzflip
Spigen Neo one case on flip 8
Love this case ! Makes the color pop, fits well and feels nice. Maybe not the grippiest case but with a PopSocket it doesn’t really matter 😬
u/Secret_Donut_8051 — 11 hours ago
▲ 136 r/puppies
Meet Sudden 🥰 14 weeks old
We have been without a dog for 2,5 years, and it’s been awful. 😞 I’ve always had dogs in my life so it’s been so empty.
My son who’s 7 also got epilepsy 1,5 year ago and last year was a nightmare for us both. On top of that he got bullied in school and was excluded all the time.
And I was exhausted and worried and everything was just revolving around these things.
Finally decided to start LIVING again, and now we have a little happy pill on four paws again❤️😍🥰. And my son will always have a friend , on rough days he can come home and just snuggle and feel that he’s been missed by his best friend ❤️
Sudden is a Maltese/yorkshire terrier/toy poodle mix ❤️
And to make things even more awesome one of my closest friends who live a few minutes walk away got his brother 😃
u/Secret_Donut_8051 — 19 days ago
▲ 1 r/Epilepsy
Sodium valproate side effects in kids
What side effects have you seen in your children from valproate ?
I’m interested in all but in particular those involving tiredness, exhaustion, bad sleep, and cognitive slowing, as well as behaviour that looks like ADHD.
Also VERY interested in anyone has gotten a lot of myoclonic jerk while sleeping from it, and or automatism looking movements that weren’t ?
My 7 y o son had his diagnosis 1,5 year ago. When they started him om AED he got way worse , we went through a number of them but he just got worse and had rough side effects , but then settled on valproate due to the least probable side effects, but since starting meds from the beginning, his not who he used to be completely. I had a very bright little guy who spoke very fast but clear, who had no problem concentrating, who wasn’t hyperactive , who didn’t have myoclonic jerks etc.
those are hard though because they Are definitely linked to how his epilepsy is doing , but I have a feeling that meds aren’t helping.
He’s absolutely exhausted most of the time when he wakes up, sleep sucks. And now after increased evening dose a week ago it’s even worse. Today increased morning dose and it’s been a mix of falling asleep and hyperactive deluxe 😳
His medication and epilepsy is really lowering quality of life. It ruins so much to be exhausted from so little all the time 😔
Can anyone recognise any of this, and what has your experience been?
u/Secret_Donut_8051 — 2 months ago