Does anyone know if it is possible to change my username please? I think I would rather use my proper name than Doggymama lol xx
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I was considering that too.
I seem to recall some security advice when I created my account that suggested you didn't use your real name.Hi, I'm Eddie.
Started with wobbly left ankle in Nov 2020. Diagnosed 22 Oct 2021, confirmed by 2nd opinion 4 days later.
Still walking and talking, and wondering what the future will bring.
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It doesn’t look as if it’s possible to change your user name. Suggest you ask MND Connect though.
I saw the warning about choosing an anonymous name, but just used my first name and initials (I’m not really Peter Pan!)Diagnosed October 2020 - See my blog at https://www.myneurodiary.com
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Originally posted by Doggymama View PostDoes anyone know if it is possible to change my username please? I think I would rather use my proper name than Doggymama lol xx
Btw, your dog is cute 😘Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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Hi all,
Thanks Ellie for tagging us in this post. For any problems or issues with the forum itself, it is best to post in the Forum Announcements & Help section as it sends us an email alert and we can pick it up straight away.
It is possible for a username on an existing account to be changed, but it's only something we can do ourselves. Obviously we wouldn't want to keep changing member's usernames all the time, once you're sure you definitely want it changed and what you want it changed to, send us a PM and we can action it.
Here are some top tips that we'd recommend to keep safe and secure:- Don’t use your full name or parts of your address or phone number
- Don’t use your email username
- Don’t use the same username and password combination, especially on financial accounts
- Don’t choose a super-odd username and then reuse it again and again — it makes you easier to track and find out information about you.
- Don’t choose a username that gives clues to your passwords such as a series of numbers/letters or the first part of a two-part phrase, such as knock-knock or starlight
- DO choose a username that’s appropriate, and not offensive, for the type of account, i.e., business, social or personal
Forum Admin.Our working hours are Monday to Friday 8:30am until 5pm
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Originally posted by Doggymama View PostHappy to keep my usernameDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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Haha Ellie, you made me smile, Barney has kept me going through this awful time, he just knows his mama needs lots of cuddles, he is so my boy!
We had an awful night last night, my husband was so terribly upset. Hard to know how to help him. He said he just wants to die, it's truly heart-breaking. His nurse is ringing this morning so hopefully she can offer some advice. Council coming out tomorrow to fit the rails, when I read on here that things move quickly, I had no idea just how fast they do. we already have another home vent appt, physio been and have ordered him a headmaster collar. His nurse is regularly in touch and he goes to clinic every 8 weeks. Can't fault the support it's amazing, but so sad it is needed. Love to you all, I know everyone has their own struggles and the difficult thing is knowing that this is the 'best' things will be as it will only deteriorate. Sorry for the 'woe is us' but fearful of the future and my husband's mental health as well as his physical health but it is the hand we have been dealt with and time for 'big girl's pants' I think. xxxCarer for my husband who was diagnosed with ALS on 15.12.21.
Trying to think of only today and tomorrow
Alison ♥
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Doggymama
Hi Alison
It is hard to know how to deal with the persons emotions, espeacially when your own are in a mess.
My husband refused psycholigical help but I get support calls from Hospice family support. It is just a listening ear not any advice.
I am an ex nurse and I feel alone and responsible for everything day to day.
I know that MND association has call support, I have phoned them for other advice.
Some/many people are on anti depressents. Both person with illness and the carers, I have read on a variety of forums.
I would defenately alert your GP to your carer situation, you need support too.
Have no personal experience of it for myself (yet) and Thomas refuses.
He does mention Dignatas and when I mention that some people last beyond a decade, he says he cannot do this for 10 years.
The emotions are different every day.
Best wishes
Donna
Carer for husband diagnosed July 2020, MND of Fail Arm TypeDonna
Carer for husband Thomas, diagnosed with MND of Fail Arm Type in July 2020.
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