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My Grandpa died in 2013 of MND hardest thing to watch your loved one die like this infront of you eyes

He is so young. I only learned of this disease this week, and I hate it. How unfair.

A horrible disease have been watching my best friend over two years slowly deteriorate . Wouldn’t wish this on anyone stay strong and keep fighting and hopefully soon they will have a cure . Bless your wife and son ❤

Praying for you and your family in Jesus name!

Ami MND rugi kono chikissa thakle janaben

How can I contact him

Pete have you heard about MND reversal? Please have a look at a man called Mark Manchester and he’s reversal story x

Which type of motor neuron disease does he have ?

Is there an update? Sept 20,2024?

There’s an American on TH-cam with ALS.

My husband Andreas and myself went through this. Such a cruel cruel disease 😢

Davis John Martin Betty Young Mark

If you have received the vaxxcine you need to report this to the yellow card scheme ,and claim compensation .MND is a side effect of the "safe and effective" 💉

What such a beautiful family and how loving you are to each other, thank you Pete for sharing your life with MND your just up the road from me i live in Chittlehampton near Barnstaple and ive just been diagnosed with PLS my symptoms began just over 3 yrs ago very similar to yourself and now i can barely walk i use a frame & have a mobility scooter. Ive been seeing my Nurologist just over 2 years but no tests showed anything up and he was totally baffled so him wanted a second opinion and i was seen last weekend by a professor of nurology Tim Harrower infact he works mostly in Exeter but attends the NDDH at weekends well after 20 minutes of him examining me and asking about my symptoms he diagnosed me with PLS MND it's very rare it's a slower disease compared to ALS. I'm 60 and have a loving husband and our 30 yr old son who has autism, adhd it's very tough and my heart goes out to you and your family, i so hope the trial works and they soon find a cure good luck and take great care of each other God bless everyone who is fighting this devastating disease 🙏ive been put on Tizanidine to relax my muscles so less stiffness and also Levodopa which helps stiffness and twitches plus pain relief. All the very best and let's all join hands and keep fighting 💪

Prayers to you and your family .

There is an awful lot of young healthy people developing MND in the last few years in the wake of the vaccine rollout

Another Rob burrows insurbraition sorry if that's spelt wrong God bless you and your family ❤️ xx

what is the hand stimulator called, god bless

ALS is not disease of people in 60s, 70s and 80s. I don't know where they got it from. I never herd of 8O yr old developing ALS. It attacks on average late 40s, or early/mid 50s. Many times earlier. We must find damm cure for this fuckin disease. Because enough is enough, nobody should be dying like that, with no hope in today's society. And doctors among themselves say that disease is the worst❤. Please donate to ALS SOCIETY, of your choice.

Oh wow Pete teached me for a while at Exeter city school he was one of kind ❤

May god bless him for long long life and get relieved of the disease

Heartbreaking to see such a fit, active young man with his life ahead of him be physically destroyed like this. This has to be the worst disease ever.

"MND is NOT going to decide my fate" I refuse to put myself and put my family through watching me slowly die so when the time is right for me I will do VSED. VOLUNTARILY STOP EATING AND DRINKING. I will choose how and when i check out NOT MND 💪😊

His wife is amazing God bless her

I'm so utterly sorry for you and your family. This is probably one of the worst diseases to negotiate (my sister was diagnosed with it 😢😢). May God be with you all.

My friend's fit and health conscious son started to experience the signs of MND when he was cycling and found that one of his feet could not push the pedal. Who could believe that within the year he was laying in bed, paralyzed from the neck down with a tube helping him to breathe and a tube feeding him. This was a young man, who would go rock climbing, work out at the gym, swim and cycle everywhere and all before that one symptom of MND when his foot could not push the pedal. To say his death was a blessing is an understatement. i hope and pray that more money is pumped into research to help find a cure for this very cruel, brutal disease. Good Luck to Pete Eveleigh, A lovely family and a loving, strong woman by his side. Hoping things are going well for him.

How are you doing now Pete? Hope the trial is working

Ben Wetten did a great job on this season, I'm really looking forward to seeing more of his work in season 3!!!!!

What a handsome man…my heart goes out to you and your wife.

Brother you great you have a great family ❤

I have incurable motor neurone disease. My entire body is slowly becoming paralysed. I am 23 years old and my father has abandoned me. I really need helps. please someone help me. God bless you always

🙏🙏🙏

I was given a diagnosis of MND in June 2022 by my neurologist. Here in the States, the diagnosis must be confirmed by a “higher level of care”. After months of waiting, I finally got a zoom appointment with a neurologist at a prestigious ALS Clinic at a university medical center in California. Early in the zoom appointment , the neurologist, (without an in-person exam or repeat testing), declared that I didn’t have MND. As my husband broke down in sobbing relief, I asked her how she could know that? She said it was because she’s an “expert”. When I further pressed her, she said that it was because I was able to stand from the sofa without using my hands. Everyone is thrilled except me, because my symptoms continue to worsen. I feel like I’m “twisting in the wind”, without the benefit of a diagnosis (of any kind) or hope for support or treatment. No other doctor will question the opinion of the expert.

I’m sorry if this is inappropriate. I was just curious of something. My father also has Parkinson’s. I am also going through a DX process of something Neurological/muscular. I was just wondering if possible how to ask you some advice? Again I’m very sorry for bothering you. Thank you for being so inspiring.

gorgeous brave guy.

📿🕊️🤍🕊️🤍🕊️🤍📿

Is it right me saying your twitches was first symptom with no weakness ? I have cfs cramp being faciculation syndrome diagnosed September but get scared my heart goes out to you and your family

Terrible cruel disease. X

So inspiring thank you for your video my husband has MND can you please tell me where you got breathing and hand equipment from… my husband is Turkish and not entitled to any benefits because of his visa but the MND association have helped us

Is MND like ALS

the more attention that can be given to the condition to increase awareness and research funding, the better. Keep fighting! I'm glad you have a great family to keep you motivated!

God bless u and ur family, Pete hope u get a cure in the very near future,,,,,,,,,,,,,,,,

Bless your hearts, I hope they find an appropriate trial for you Pete and you can improve. I’ll keep following your progress and want to see you healthy again in the very near future. Good luck hun. 🍀

Cruel disease.

Life is so cruel what a handsome man and his lovely family a awful disease

So wish a cure can be found quickly.

Praying for a healing for him amen

I'm exactly the same. Started with muscle fasciculations around 3 months ago, now i have weakness in my left arm and right leg. Keep almost falling over and dropping everything. I'm terrified. I had two spinal surgeries last year, I'm sure it's triggered it. I'm at the consultant 15th of August. I'm 44 xxx

Life is so unfair...

This family are truly inspirational. What a cruel unforgiving disease. That little boy is a credit to you both, a little darling, eloquent and so well spoken. I pray for your recovery, and hope the interventions are positive. The mind is very powerful, stay strong and together.... God Bless you all on this journey 🙏❤️🙏