Genetic testing eg Ataxia or Hypertrophic cardio... - Ataxia UK

Ataxia UK

4,037 members4,576 posts

Genetic testing eg Ataxia or Hypertrophic cardiomyopathy

scruffycat profile image
10 Replies

Who has had it? who did it? Do you need other family members? How were you put forward?

Written by
scruffycat profile image
scruffycat
To view profiles and participate in discussions please or .
Read more about...
10 Replies
wobblybee profile image
wobblybee

Hi Scruffycat :-)

I had to Google the second one :-) no-one in my family has been tested for this.

At the point of diagnosis of SCA, I was asked if I'd like to donate DNA for research

purposes, and I did. That was in 2011 and I was considered Idiopathic at the time.

Last week I was told a connection had been made with a rare gene. So, proof that we can put faith in research :-) xB

eileen200271 profile image
eileen200271

Hiya Scruffycat. My son has been tested. His grandad and dad have been diagnosed with SCA6. He saw his GP who sent a referral letter to a clinic in Leeds. The letter was sent last August. His appt was in January. They would not do the test that day - they sent him away to think about it!!! Got an appointment in March and the took blood, said it would be 4/6 weeks. After 8 wks he rang and asked the result but they wouldn't tell him over the phone. He received a letter in the post telling him the result was positive. Not really the best experience in the world but as my son said - I knew it would be positive, just needed the confirmation!! Hope this answers some of your queries.

Take care, x

scruffycat profile image
scruffycat in reply to eileen200271

sounds like a journey full of pitfalls and twists'n'turns but,if you last that long, you get there in the end. Maybe.

Thanks

eileen200271 profile image
eileen200271 in reply to scruffycat

Yr welcome 🎉🎉🎉

scruffycat profile image
scruffycat in reply to eileen200271

Were any other family members involved?

eileen200271 profile image
eileen200271 in reply to scruffycat

Hiya. No. He just went to his GP and asked to be referred as for any other medical problem. E 💜

eileen200271 profile image
eileen200271

Hiya Scruffycat. My son has been tested. His grandad and dad have been diagnosed with SCA6. He saw his GP who sent a referral letter to a clinic in Leeds. The letter was sent last August. His appt was in January. They would not do the test that day - they sent him away to think about it!!! Got an appointment in March and the took blood, said it would be 4/6 weeks. After 8 wks he rang and asked the result but they wouldn't tell him over the phone. He received a letter in the post telling him the result was positive. Not really the best experience in the world but as my son said - I knew it would be positive, just needed the confirmation!! Hope this answers some of your queries.

Take care, x

Litty profile image
Litty

A long time ago my Dad, I and my sister were tested. It was back in 1995 and they had just discovered the test. At St Thomas Hospital they discovered my Dad had SCA1. I wanted to know if I had it because I had a young family. I was referred by my GP to

geneticalliance.org.uk/serv...

they are excellent and gave me and my husband several months of counselling (which you need. It is hard knowing you have it coming for definite) before they tested me.

I now go to the London Ataxia Centre and they offer testing. My kids are in their 20s and since my ataxia will not affect them until they are in their 40s their view is that there is nothing they can do and get on and live their lives to full. They may die of something else before anyway.

Hope this helps : )

scruffycat profile image
scruffycat in reply to Litty

As you say, 1995 was early days. The trouble is Ataxia remains a bit of dark art.

Life,as they say, is a bit like a box of chocolates. You never know what y're going to get!

scruffycat profile image
scruffycat

The post code lottery is alive and well, in this  country. Often lead by silly things like budget, rather than actual need.

You may also like...

Genetic Ataxia

My daughter who is 11 years old has been ataxic since she was 13 months old. She attends a...

Non Genetic Cerebellar Ataxia

experiences with their Ataxia. I look forward to hearing from you all. Thanks

Genetic testing and family planning

a right to be here and you have to die of something. Also IF our families had known about ataxia and

Spinocerebellar ataxia type 6 test

advice. My Aunt has just been tested positive for spinocerebellar ataxia type 6, and my Mum has all...

ataxia

as you do, I am now 61 and was told the same as you its very progressive even through it has...