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appalachiablue

(42,913 posts)
Mon Nov 18, 2019, 10:25 PM Nov 2019

Woman Who Inherited Huntington's Disease Sues NHS: Another Asks 'Do I Test?'

-- BBC News, 'Huntington's disease: Woman who inherited gene sues NHS,' Nov. 18, 2019.

A woman who was not informed that her father had a fatal, inherited brain disorder has told the High Court that she would have had an abortion if she'd known at the time of her pregnancy. She is suing three NHS trusts saying they owed a duty of care to tell her about her dad's Huntington's disease. Any child of someone with the condition has a 50% chance of inheriting it. Doctors suspected the diagnosis after her father shot dead her mother and was detained under the Mental Health Act.

The father tested positive for Huntington's Disease, which is caused by a faulty gene and leads to the progressive loss of brain cells, affecting movement, mood and thinking skills. It can also cause aggressive behaviour. He told doctors he did not want his daughter told about his diagnosis, fearing she might kill herself or have an abortion if she found out.

50:50 chance: The claimant is known as ABC in order to protect the identity of her own daughter, who is now nine. ABC only found out that her father had Huntington's Disease, a progressive, incurable condition, four months after giving birth..

Read More, https://www.bbc.com/news/health-50425039
_______________________________________



- Jackie with her brother Mark.

-- BBC, 'There's A 50% Chance I Have A Fatal; Disease.' If you could see how the rest of your life might play out would you want to? *Jan. 23, 2018. Jackie Harrison has a 50-50 chance of a disease that has killed her mother, uncle and grandfather. Should she take a test to find out whether she will get it too - and could she cope with the result? The BBC's Sarah Bowen has been following her story.

It's rare for a day to pass when Jackie Harrison doesn't wonder if she's inherited the faulty gene that could lead to her developing Huntington's disease, a condition that causes certain nerve cells in the brain to waste away and slowly robs you of the ability to talk, to walk, to move, to think, to swallow. There is no treatment for Huntington's and no cure.

Jackie is 51 and lives in Brighouse, a small, industrial town in West Yorkshire, with her partner of 30 years, Tony, and younger brother, Mark. When Jackie was 12 her mother, Jean, who'd been a teacher, died from the disease at the age of just 48. Her father left the children to be brought up by their grandmother, 78-year-old Edith, who had already lost her husband to Huntington's. Within two years Edith's son, Barry - Jackie's uncle - had also died.

"I've not had a normal life, it's taken everything from me," Jackie says. "I don't know what it's like to have a mum and dad, to have that stability." Jackie wanted to become a teacher like her mum and grandmother, but when Edith died it was up to Jackie to run the house and look after her brother. She got a job and managed to keep a roof over their heads while Mark took his exams at school. Then, when Mark went to university, Jackie was able to work part-time and study herself - gaining a degree and doing a teaching diploma.

But then Mark developed Huntington's and for the past 10 years Jackie has been his full-time carer...

Read More, https://www.bbc.com/news/stories-42627782

5 replies = new reply since forum marked as read
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Woman Who Inherited Huntington's Disease Sues NHS: Another Asks 'Do I Test?' (Original Post) appalachiablue Nov 2019 OP
That is so very tragic. Laffy Kat Nov 2019 #1
Beyond words. In reading about this months ago I came across appalachiablue Nov 2019 #2
Well the article above does have as happy an ending as possible. Laffy Kat Nov 2019 #3
Yeah, Huntington's is brutal. That's what killed Woody Guthrie. Clash City Rocker Nov 2019 #4
It will be interesting to see if the privacy laws are compromised by this case. Chemisse Jan 2020 #5

appalachiablue

(42,913 posts)
2. Beyond words. In reading about this months ago I came across
Mon Nov 18, 2019, 10:46 PM
Nov 2019

the work of a prominent scientist researcher whose family has this condition. She's made excellent progress and is devoted to the issue, naturally. 'The thread is finally broken her family.' I'll post the info. if I can find it.

Laffy Kat

(16,524 posts)
3. Well the article above does have as happy an ending as possible.
Mon Nov 18, 2019, 10:51 PM
Nov 2019

Even though neurological diseases are almost always sad, I do find them fascinating to read about.

Clash City Rocker

(3,541 posts)
4. Yeah, Huntington's is brutal. That's what killed Woody Guthrie.
Mon Nov 18, 2019, 11:58 PM
Nov 2019

I read a fascinating biography called “Woody Guthrie: A Life” many years ago. It mentioned that Huntington’s accentuates the mental qualities of the person who has it, and therefore, it may be why Woody was such a prolific songwriter.

Chemisse

(30,999 posts)
5. It will be interesting to see if the privacy laws are compromised by this case.
Wed Jan 1, 2020, 06:53 PM
Jan 2020

Clearly the organization could not tell her about her father's disease against his wishes. To rule in her favor would have a big impact on the privacy laws covering a person's medical records.

Sad though this is, I don't think I'd like to see the privacy protections weakened.

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