New here. SIL has PKD, I'm worried about my children's kidney scans. Anyone been through similar?
guweeze
Community Member Posts: 1 Listener
Hi
My SIL has PKD. She is the first in her family to have it, as far as we know. Her parents had scans of their kidneys and liver which showed nothing.
Her brother, father of my children, hasn't had a kidney scan yet. I'm quite anxious about it, obviously regarding my children.
Has anyone been through anything similar? Or does anyone have any opinion on the situation?
Many thanks
Louise
0
Comments
-
Heya @guweeze and welcome to the community.
I'm afraid I don't know a great deal about PKD, but I understand your concern regarding the scans. I'd try not to worry too much as the gene mutation tends to come from parents and sometimes can just appear randomly. I'm hoping some of the community will be able to put your mind at ease with their input soon.0
Categories
- All Categories
- 16.3K Start here and say hello!
- 7.7K Coffee lounge
- 122 Games den
- 1.8K People power
- 185 Announcements and information
- 25.6K Talk about life
- 6.2K Everyday life
- 422 Current affairs
- 2.5K Families and carers
- 887 Education and skills
- 2K Work
- 610 Money and bills
- 3.8K Housing and independent living
- 1.2K Transport and travel
- 674 Relationships
- 1.6K Mental health and wellbeing
- 2.6K Talk about your impairment
- 883 Rare, invisible, & undiagnosed conditions
- 945 Neurological impairments and pain
- 2.3K Cerebral Palsy Network
- 1.3K Autism and neurodiversity
- 41.4K Talk about your benefits
- 6.2K Employment & Support Allowance (ESA)
- 20.5K PIP, DLA, ADP & AA
- 9.4K Universal Credit (UC)
- 5.4K Benefits and income
