
Lisa Nainggolan
Contributor and Editor at Freelance
Freelance, award-winning,, medical journalist and editor. Mum of two, who values family, friends and a good book. Adult human female. Views are my own.
Articles
-
Dec 12, 2024 |
re-solveglobalhealth.com | Lisa Nainggolan
Over-medicalisation of pregnancy and childbirth has escalated in recent decades. A new approach that puts midwives at the centre of healthcare delivery is set to improve outcomes for mothers and babies. A midwife gives a baby back to the mother.
-
Sep 27, 2024 |
mdedge.com | Lisa Nainggolan
“I’d probably be a quadriplegic,” Dean J. Kereiakes, MD, an interventional cardiologist, said when asked what would have happened if two top neurosurgeons at his hospital hadn’t rushed him to the operating room (OR) for a cervical decompression in February this year. Dr. Kereiakes had orthopedic problems for years due to the heavy lead aprons he wore in the cath lab. He regularly dosed himself with steroids for disc pain so he could stand up straight and continue to do procedures.
-
Sep 3, 2024 |
re-solveglobalhealth.com | Lisa Nainggolan
Healthcare workers are on the frontlines of a global battle against abortion stigma, which lingers even as legal access expands in countries like Mexico, India, and Colombia. Educating and supporting these professionals can ensure they provide safe, non-judgmental care. Abortion stigma is pervasive for women seeking abortion and for healthcare workers conducting the procedure.
-
Aug 1, 2024 |
espanol.medscape.com | Lisa Nainggolan
HELSINKI. Se ha identificado un nuevo gen para la enfermedad de Parkinson de aparición temprana, un descubrimiento que los expertos y expertas creen que tendrá importantes implicaciones clínicas en un futuro no muy lejano.[1] Se identificó una variante en PMSF1, gen regulador del proteosoma, en 15 familias de 13 países alrededor del mundo, con 22 individuos afectados.
-
Jul 17, 2024 |
mdedge.com | Lisa Nainggolan
A new gene for early-onset Parkinson’s disease has been identified, a discovery that experts believe will have important clinical implications in the not-too-distant future. A variant in PMSF1, a proteasome regulator, was identified in 15 families from 13 countries around the world, with 22 affected individuals. “These families were ethnically diverse, and in all of them, the variant in PMSF1 correlated with the neurologic phenotype.
Try JournoFinder For Free
Search and contact over 1M+ journalist profiles, browse 100M+ articles, and unlock powerful PR tools.
Start Your 7-Day Free Trial →X (formerly Twitter)
- Followers
- 1K
- Tweets
- 2K
- DMs Open
- No

RT @DrEJBrearley: @SexMattersOrg @HouseofCommons @bphillipsonMP @UKLabour @KemiBadenoch @ForWomenScot Absolutely barnstorming speech and gl…

RT @SexMattersOrg: @HouseofCommons @bphillipsonMP @UKLabour “This is not the end of the matter, but the beginning of the end.” @KemiBade…

https://t.co/Y1OajajN05