Introduction

[Suefromwakey]

If only we were not all under house arrest!!

[richard]

Hi Sue. Yes I am still able to eat, drink and chat just fine and no immediate concerns there but my legs and walking are gone. Is this a precursor to you inviting me for a drink, dinner and a chat?😂

Richard

[Lynne K]

Hi Peter, a warm welcome. Everybody will get a big shock when they’re diagnosed and it sure does take time to get your head around. I hope that you have a
s good services down under as we do here.

Our retirement plans were thwarted by my MND but we do whatever we can to stay upbeat. Take care, Lynne

[Suefromwakey]

Hi Richard,
your symptoms sound remarkably like my husbands - he started falling 2016, started seeing consultants in 2019, had loads and loads of tests, but still awaits a true diagnosis - we have been on a merry go round of "maybe its this that or other" his legs practically gone now

Are you able to eat/drink and speak as normal? My husband is ok on that score

Sue

[denise]

Hi Peter
it's a shock I know. I thought something was wrong with my husband. We had retired to Portugal. Now I just want us to get back to the UK so we can be close to friends and family. I have made some wonderful friends here. This forum is not just for you but your family and friends. I hope we can be there for you.
Denise xx

[Deb]

A warm welcome to the forum from me Peter,

The diagnosis is such a shock and I found all the well meaning advice from professionals overwhelming. I couldn't believe they were talking about me and I spent ages googling alternative explanationfor my symptoms.. I guess its a denial and I wasn't ready to accept things.

Things do get better as you adapt both physically and mentally. There are still good times to be had.!

Take care of yourself,
Love Debbie x

[Ellie]

Welcome to the Forum, Peter.

[Shaun]

Hello Peter and welcome,
it is a shock but given a bit of time you will come to terms with it, all my retirement plans changed, so we have adapted them, it was always our plan to move to the coast , so instead we bought a holiday home now, so we can enjoy it whilst we can, rather than in 5 years or so, plans can change just think a little differently. Don’t let this change who you are, do what you want, as best you can.
shaun

[Barry52]

Hello and welcome Peter,

We have a few Australians on this forum and the collaboration with the UK and Australian scientists over the past few years has brought hope of new treatments. Ask any questions here and someone will offer advice.

[matthew55]

Hi Peter. It is a great shock not just for you but everyone who knows you. I deal with it by just saying it is what it is. On the plus side you get more time to arrange things than others. Stay Strong Matthew 😁x

[Peter Carty]

Thanks jd

[jd58]

Welcome to the group Peter

[Peter Carty]

Thanks Richard
it’s heartening you are still ticking along!
one of the scariest parts is how short a life it can be. I’ve had a limp on right side since May this year but other symptoms since lots of tests which just eliminated everything else.

[richard]

No. My first symptoms were five years ago this month. I was having trouble walking. I was told in early 2016 that is was most likely to be MND and then embarked on to loads of tests. I was formally diagnosed in 2018. I have slow progressive MND. I can no longer walk as my legs are useless. Occasional severe cramps in arms and upper body. The fist part is to accept you have this horrible disease , presently there is no cure but over the last 12 months there have been loads of advances.

Remember keep smiling and that whilst you are the patient your family are also suffering with you.

Richard

[Peter Carty]

Thanks Richard
you're newly diagnosed too?