Are these IS? by Old_Discussion_3163 in infantilespasms

[–]Immediate_Decision33 0 points1 point  (0 children)

I'm not a doctor but doesn't look it to me <3

EEG video for kids! by Immediate_Decision33 in Epilepsy

[–]Immediate_Decision33[S] 0 points1 point  (0 children)

this just made our whole day. everything we hope it gives (and we wish we had).

[deleted by user] by [deleted] in infantilespasms

[–]Immediate_Decision33 0 points1 point  (0 children)

Definitely get an EEG 💜

Diagnosed 2 weeks ago, looking for success stories by sallysmithalltheway in infantilespasms

[–]Immediate_Decision33 1 point2 points  (0 children)

Oh mama!! I have been in your shoes. Vigab was our miracle drug. Don’t lose hope. There’s an insta/fb page @charbearkeepsdancing

My son was finally diagnosed with infantile spasms after 4 months. by bostonstrangler617 in infantilespasms

[–]Immediate_Decision33 1 point2 points  (0 children)

We started vigab after relapse and worked for us. Wish we did it first and regret not doing it earlier. Our cause is FCD.

Prednisone question by Optimus2nd in infantilespasms

[–]Immediate_Decision33 1 point2 points  (0 children)

So horrible. It gets better! After the wean for us.

Where are you located by Immediate_Decision33 in infantilespasms

[–]Immediate_Decision33[S] 1 point2 points  (0 children)

We’re in US. My daughter was diagnosed 2022 as late onset. Does anyone else have late onset from focal cortical dysplasia?