Видео

David, we so enjoyed your account of using SpeakUnique. It is a truly worthwhile and totally helpful way to help with communication. We loved your presentation and are so proud of your contribution in encouraging other people who may be in the early stages of MND to really feel motivated to bank their voice. It's so good to know that banked voices not only help the initial banker but can also be used by other people too. We look forward to seeing your ventriloquist trick!

What you feel on your tongue before slurred your speech.

David you are lovely and so is your voice. I really enjoyed hearing what you had to say and your cheeky smile. I’m under investigation by neurology and wait to find out what tests are next to exclude things. I have symptoms of MND or symptoms mimicking MND. I would definitely get my voice banked if it comes to that. Thank you and God Bless, I’m Scottish too!

Hope you are doing well Jim. 💕

Such a tragic condition. I pray that research will find a cause - helping, if possible to prevent development. So sad. Lovely man. 💕💕

The look in the eye Is always the same. No matter the situation. God bless.

God bless you Mark my brother in law has just been diagnosed with zMND.❤

I am sure u will get a lot of likes

What a lovely guy and family x

Incredible video Mark, thanks for discussing and highlighting this horrible disease which affected a good friend of ours. You are a brave man and I wish you and all the family all the best in this moment and hopefully a long time in the future. Take care 👍

I can't imagine how tough this must be for Mark and his family, MND is a devastating disease, one which I'm currently showing symptoms of myself. Hoping for a cure ASAP. Wish you and your family all the best mark.

Praying for this man. Brings back memories of my friend David Balmer. Stay strong big man

Nice one fergie. Where this man pulls his courage from is beyond me. Sending love love mate and to your extended MND family. Legend 💪

What dates do you have

Heartbreaking 😢 Great he’s getting help and has family and friends around him though.

I’m currently doing the 15000 steps a day in January for MND Scotland. Donations are building. Keep up the great work. 🥹🏴󠁧󠁢󠁳󠁣󠁴󠁿

Hey @Gemma. My mom has same symptoms. How is your mom now.

So sorry for your diagnosis. This is a devastating disease. I lost my sister 10 months ago from ALS. Prayers for you

I am really sorry to hear this, i just been notified. Steve was and still is a very respected man who I had alot of time for while working with him in the department. Big Hearts and Scotland fan. From the only Berwick Rangers fan you knew, my heart go's out to you my friend....very brave man.

😴 Promo'SM!

So many goods was said about Doctor Madida on RUclips and i was desperate to get cured of herpes virus. My greatest joy was that Dr Madida was a genuine and safe person who did sent me the herbal medicine I requested for, I used it as he instructed me and after then all the symptoms I use to have all stopped. I went for another diagnosis and my doctor confirmed me Herpes virus Negative after so many and strictly test I undergo. I don't know about all other doctors but Dr Madida is this greatest herbalist I have ever known.

To live is more important than to die. Even with less hope or fortune. For a living dog is better than a dead lion. My name is Jennifer Garcia, I am 69 years old. It all started toward the end of the year 2018 when I was diagnosed with amyotrophic lateral sclerosis [ALS]. I became a little child who does nothing but to depend on others for everything. I barely move my feet and hands myself. My son of blessed memory Anthony who passed on last year tried all he could to see me back on my feet but all his effort seemed impossible. The doctor said I will have to live like that for the few months I will spend on earth. The pastor gave me hope and prayers but it got to a time that I lost my faith as my health deteriorated. I began to await death by installment but on a fateful day when I went out for my normal therapy at the clinic, my very first boyfriend Stanley saw me in a wheelchair as my daughter pushed me in and he came with so much expression of disappointment on his face. He promised to go on a research on the internet to find if there is an alternative cure. He stopped at nothing until he discovered a post in google page by Darren Kent testifying how he got cured from ALS by Dr. Sani natural herbal remedies. We contacted him through his Email and WhatsApp. He told me that he has herbal healing remedies to cure not only ALS but also other incurable but management diseases. I believed or trusted him because I was left with no choice. I sent him money and He prepared his herbal mixture tonic, herbal cream and healing oil and sent them across to me. He gave me instructions which my daughter took seriously. After two weeks of treatment, I began to notice some great changes like I was able to talk clearly, eat, drink and move my hands and legs gradually. The third and fourth week I got cured. THE KEY POINT IS THAT I CAN DO THINGS NOW WITHOUT NEEDING SUPPORT OR BUGGING ANYBODY. Dr. Sani never asked me to advertise him but I think it’s what I should do to make our world a favorable and disease free one. Sharing is Caring. You can contact him today by E-mail: perfectherbalcure@gmail.com or call his tel; +2348118184266. I so much love this Dr. Sani Hassan for I owe my life to him. He is so kind and polite. Thanks for viewing.

Hello everyone my dad was diagnosed with motor nurion disease Als and the told us there's no cure for it. But i want appreciate dr ehimare who reverse my dad Als with his herbs medicine treatment and i will continue to testify about your treatment and God will bless you more. And you can also reach Dr via WhatsApp +23490 2734 9748 or email (drehimareherbalremedyhome22@gmail.com)

Hello all, I am from Nepal and my father has mnd and it's been more than 2 yrs that we had known about the case. Now, he is having lots of problem in breathing and movement has become almost zero. However, my mom and me everyday we do some physical exercises in home and also help him to do some movement. We have been continuously giving a specific medicine Branton 500 and other few medicine but the situation has been worse than showing some good sign. If anyone has some idea I'd be happy and hopeful.