Three Years!

[@bhagwatshah]

My dad has had MND for 23 years. It's been a long and hard journey. BUT, with the love and support of the family, he continues to have a happy life.

[@peanuteversoj6642]

How is your dad? My dad passed only a few months after he was told he had it.

[@dingbat102]

Lucy, you are an incredible human being. You're impacting more than you know

[@darenmorley4598]

Just seen your documentary on the BBC, you are a truly amazing person, with a wicked sense of humour. The amount you have raised for MND is fantastic . Your strength is inspiring, I run for charity on a regular basis next time will be for MND! Thanks for raising awareness.

[@stephenshackleton7173]

I think you're incredible Lucy, watching your documentary left me in tears and I hope you're OK and happy x

[@johncrabtree1193]

Second time I've watched this just wow as someone with hydrocephalus thank you your challenge is so much so much greater than mine thank you. So hope that a cure is found. Lost my cousin to a brain tumour keep fighting.

[@keithhutchins8803]

I'm so very happy to see you again Lucy. I can't began to tell you how much I think, and worry about you. I also have mnd so I understand how you feel.

[@philipbrindle4283]

what a fantastic lady. It is difficult to express the admiration I have for Lucy. Her determination to live life and deal with the problems caused by MND is remarkable. I have MND but am much older than Lucy, for her to have been diagnosed at such a young age is awful, but the way she has dealt with it is just amazing.

[@MrSmid888]

The best personality and great Scottish humour on your documentary.Bless you and your family and friends X

[@soylentgreen505]

Hello lucy! I found your story very moving! I do hope you find the strength when you need it most! Keep smiling & laughing! Your amazing woman!

[@GlasgowMick50]

You're an inspiration Lucy, all the best x

[@Lazarus_Kumi]

Stay strong sweety. You are an amazing human being !

[@TheMrturn1]

Aw Lucy, to see you there battling with a disease which is taking so much from you, so cruelly at such a young age... at yet there you are shedding a tear for those who didn't last as long as you... it's amazing to watch. You have quite a good heart, and are filled with a good soul. Be proud to be such a thoroughly right person. Better to have lived your life with your heart and through your eyes for however much time you are given, than longer with another's soulless heart and blank eyes. I don't have mnd but the disease just breaks my heart and so I try to stay mindful of those like you that are hurting... so every here and there I stay current with folks fighting this wretched monster of a disease. I hope you keep defying the odds and live a long full life.

[@BlueITagain]

Lucy, you let it out, try stay strong and we will stay strong for you and support you.Two close friends and family member have been through MND.I know I need to do my bit to help raise awareness and a cure to this god awful diesease.Yhinking of you , your friends and family as always.You keep on fighting girl!xxx

[@burropoco]

Lucy I watched your documentary on the BBC. You're an inspiration. You've channeled your energy and effervescent personality into raising awareness and being proactive. I'm hoping that you're blessed in due course for this. I'm hoping for a good outcome in some way. In the meantime please keep fighting and stay positive. Best wishes to you and your loving family.

[@paulbennett4548]

Hi Lucy, just wanted to thank you for your strength and good words. Our daughter has just been diagnosed with MND the irony is that we have just found her last year after fifty years. She has had a very good life up to this point. We are very glad that we found her and will share the time we have., as you said things happen for a reason and we are just glad that we have whatever time is allowed us. Your words will help us try and understand. Much love and peace, Paul & Sue

[@calumanderson6857]

Hi Lucy. Just watched your documentary which was inspirational. Well done for all you're work in raising awareness for this awful illness. Wishing you well.

[@LucyQuinn94]

Hi Lucy, my name is Lucy too! Ive watched your videos and just wanted to say how inspirational you seriously are, im 22 and couldnt imagine going through it myself. My father got diagnosed with MND last October and over the past year hes been incredibly unlucky and has lost his ability to do many things, its heartbreaking to even live with someone going through this horrible disease so i can't even begin to imagine how you do it. I just wanted to wish you the best and hope the progression has slowed down and you continue to fight the odds!

[@kanwal158]

How is your father now dear

[@geoffperfitt6791]

The world wishes you, and others like you, well Lucy. In our thoughts. Keep fighting.

[@MarianaCamposCarvalho]

you really helped me here down in brazil to change perspective today. thank you and much energy to you!

[@abhijeetsinha7172]

Lucy life what we see is sometimes not comes to us.There are people who loose life by self just due to life problems.See yourself you are taking life as it comes.your are a true champ.you are living in present and that is the best thing we human can do.And no one can hold the life..smile and be like that.Dont get depressed because sometime life dont give us the options.I salute you Lucy.Bless u..love

[@pauldavison7105]

Lucy just watched your documentary. Your so beautiful inside and out. Stay strong , I know it's hard, please let people you meet enjoy you as Thier lives will be fuller having known you even if it may only be for a short time.

[@umarzamanuk]

Dear Lucy, you are a amazing person incredible woman stay strong

[@DW-lx9wt]

Just saw your Beeb documentary and thought I'd stop by, subscribe, and say hi. Kind regards, Dave.

[@johncrabtree1193]

third time watching this your an inspiration as someone with hydrocephalus 🙏

[@obsoletemachine80]

You are an inspiration....Keep fighting.

[@Sub-515]

Lovely inspiring girl. You are amazing. I wish I had the magic to grant your wishes.

[@Cruella-Deville]

I think the MND society has missed a opportunity when they raised so much through the Ice Bucked challenge. There should be a follow up from the society about the research that is being done. The publicity awareness would be good they have missed a window of opportunity. What do you think Lucy.

[@christellevecchio]

Hi Lucy, I've been wondering how you've been going. It's lovely to see a video from you. Glad your doing ok. Has your progression slowed? I have a friend going through this and he hasn't been very lucky soo far 😔 what are you still able to do/not do?

[@fastbeanbaglah8762]

Watching your documentary you are awesome

[@shopgirlygm]

Hi Lucy, I'm just watching your documentary and wanted to get in touch. I have cmt disease (a nerve disease with similarities to mnd), I'm 30 and have 3 young kids. I'd love to chat to you and talk about what life is like in a wheelchair. Xx

[@johncrabtree1193]

Keep fighting

[@gmdn123]

What an amazing woman! Why is life so damn unfair?

[@muggz73]

How is your condition now?

[@hemantmudgil9319]

hello lucy ,i know it sounds crazy but can we talk ?? My intention is not to spam or anything ,just need to talk .

[@meentaalmaan]

😘😘😘😘😘😘😘😘😘😘😘😘

[@kevinaroca1708]

Lucy the only thing I can tell you is set your eyes on Christ, he can heal you, believe him, there is nothing impossible for him, trust him and he will give you peace and health, I know this is hard for you, but remember there is someone who is bigger than us, he can deal with everything, don't give up and God bless you so much