
Sally Jackson
Co-founder and Honorary Board Member of KIF1A.ORG, the patient-led foundation advancing treatment for KIF1A-Associated Neurological Disorder, which she and her husband Luke Rosen founded after daughter Susannah's diagnosis.
1
APPEARANCES
1
PODCASTS
012
DEC 30
JAN 6
JAN 13
JAN 20
JAN 27
FEB 3
FEB 10
FEB 17
FEB 24
MAR 3
MAR 10
MAR 17
MAR 24
MAR 31
APR 7
APR 14
APR 21
APR 28
MAY 5
MAY 12
MAY 19
MAY 26
JUN 2
JUN 9
JUN 16
JUN 23
JUN 30
JUL 7
JUL 14
JUL 21
JUL 28
AUG 4
AUG 11
AUG 18
AUG 25
SEP 1
SEP 8
SEP 15
SEP 22
SEP 29
OCT 6
OCT 13
OCT 20
OCT 27
NOV 3
NOV 10
NOV 17
NOV 24
DEC 1
DEC 8
DEC 15
DEC 22
DEC 29
JAN 5
JAN 12
JAN 19
JAN 26
FEB 2
FEB 9
FEB 16
FEB 23
MAR 2
MAR 9
MAR 16
MAR 23
MAR 30
APR 6
APR 13
APR 20
APR 27
MAY 4
MAY 11
MAY 18
MAY 25
JUN 1
JUN 8
JUN 15
JUN 22
JUN 29
JUL 6
JUL 13
JUL 20
JUL 27
AUG 3
AUG 10
AUG 17
AUG 24
AUG 31
SEP 7
SEP 14
SEP 21
SEP 28
Aug 26, 2026
Realities of the Nano-rare: Siblings, Unfairness and Hard Truths with Sally Jackson
17:36
17:49
17:54
18:08
18:13

Sally JacksonGUEST
Um, and we had a lot of sort of moments where it was, um, oh, she was just, just scraping by for those milestones.

Sally JacksonGUEST
And then, oh, like, you know, three days into the point where I was like, "Oh, I wonder if she would do it.

Sally JacksonGUEST
She would roll." Or we, you know, we even had a, a, you know, PT come in and do an evaluation, and she goes, "Well, let's just try putting this toy in this direction and see if we can get her to roll that way and actually make it happen." And before we could get worried, she was there and she made it.

Sally JacksonGUEST
So we had a lot of these sort of, great, I think we're gonna, I think we're gonna be okay.

Sally JacksonGUEST
You know, I, I, we'd done, um- With some research into this, uh, re- RIE, Resources and Infant Education, that was really about sort of, um, empowering your baby and talking to them all the time and making sure that they were doing things on their own timeline.
