Jack Osbourne's BBC Lifeline Appeal for the Multiple Sclerosis Society - BBC One
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- Опубліковано 12 вер 2024
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Watch the BBC first on iPlayer 👉 bbc.in/iPlayer... www.mssociety.o... TV Personality Jack Osbourne presents an appeal on behalf of the Multiple Sclerosis Society, the leading UK charity providing vital support for the thousands of people living with MS, as well as their family and carers. Jack talks from the heart about being diagnosed with MS just over a year ago and the impact it's had on his family.
The film also features Lynsey, who looks after her four year old daughter whilst also coping with MS. Some relapses can leave her barely able to move. Living with MS can put a serious strain on family relationships, but Lynsey talks about how the MS Society provided support to enable her to maintain her independence, and to live a full family life.
Please donate by going to the website mssociety.org.u... and clicking donate or by calling 0800 100 133.
Or if you'd like to post a donation please make your cheque payable to Multiple Sclerosis Society and send it to MS Society, MS National Centre, 372 Edgware Road, London. NW2 6ND
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I adore Jack. And his work raising awareness for MS is truly to be applauded.
There are several factors in reducing MS naturally . One place I discovered that succeeds in merging these is the Denelle multi care (check it out on google) definately the most helpful blueprint i've seen. Check out the great information .
Please pray for all the persons suffering MS and their family!!! I am a wife of a great man suffering this disease
Jack Osbourne has grown up and has become a pretty decent human being and a stand up guy! I hope they find a cure for MS (Multiple Sclerosis). I remember the sad decline of Annette Joanne Funicello (October 22, 1942 - April 8, 2013) an American actress & singer. Funicello began her professional career as a child performer at the age of twelve. She rose to prominence as one of the most popular "Mouseketeers" on the original Mickey Mouse Club. She finally passed away in 2013 after many long years of living life with this horrible, disabilities making disease. Slowly dying, losing her bodily functions one at a time over the years, finally, unable to walk or speak, her body completely unfunctional, all the while she inside was fully aware of what was going on outside her body.
Recently I have been counting everything steps everything I don't take anything for granted I look at flowers trees the clouds moon everything and it's a beautiful planet we are on remember that :)
Thank you. Jack you are a inspiration to me your doing so good with the awareness, an I have had MS for 20 years now an it keeps getting harder because you can't do things you use to, an it takes its toll on you an your family , I wish some people would understand, I Hope they come out with a cure soon , Thank's again for everything you do 😊
He's been helping control his symptoms with eating Paleo style. I really admire him for having the courage to share his story and raise awareness of MS.
My sister is diagnosed with this horrible illness☹️ she's currently in relapse, I wish I can take it away from her. More than 6 years ago, when she was diagnosed that's when MS hit her body hard ☹️ she lost alot of weight she looked skin and bones☹️ she was wheelchair bound and in alot of pain because I remember she was prescribed narcotics , and she never wants pain medication. It was bad. So she did therapy, they thought her how to walk again ☹️ she got better ❤️ now the ms is in full blown relapse.... Please pray for her pray 🙏🙏🙏🙏❤️❤️❤️❤️ thank yall
I have MS and I refuse to let it beat me it's hard cuz you never know what that next relapse will bring I have my good days and I have my days where I can bearly move but we live on day by day
Attitude of gratitude so many times I want to blame it on my MS and it's normal it feels awesome!!
He is brilliant on Dancing with the Stars in America watch the videos he has grown up allot. Must be hard to live with an unpredictable condition like that.
Nice job on this video & fundraiser. Best wishes Jack!
mucha luz para las personas con esta enfermedad!!..por favor, necesito que traduzcan este documental al castellano...!
I love Jack :)
I was misdiagnosed 4yrs ago. I didnt know what m.s.was but at the time neighbours was running a story and susan in it was having a relapse. Her walking was the way i was n i told my health visitor that i thought i had m.s. I eventually got sent to hospital only to be told there was nothing wrong with me! After about 2weeks in hosital i was given a lumber puncture after which i was told i had m.s. I have had quite a few relapses again being told by my specialist that i wasnt n ended up hurt mysel
Why are we still living with this? 2.5 million people are affected worldwide now, this can be passed to children and no answers have been found. We need a cure!
i just had the optic neuritis problem last week . hope i dont have ms
There has been times when i drive and I go blind but my eyes are open it's weird but I keep driving because I know my route home it's like I'm blind but I see I can't explain /:
I appreciate Jack bringing awareness to MS, but the fact of the matter is that the MS society focuses on Drug Therapy to treat MS...(which can be extremely harmful for us) I've been to MS meetings and had top MS Dr's and MS society leaders tell me that the only focus for the next few years for the MS society will be on approved MS drug therapies...I explained my story - symptom free over 10 years going with alternatives and they said they were happy for me, but the MS society as a whole will not be focusing on anything but Drug Therapy. Now why is that? People we need to wake up, the Dr's are not interested in our cure - only making life long customers. They make millions and millions off us staying sick! I've been living with MS over 25 years - if I didn't change and go with alternatives I would still be suffering, debilitated and have no quality of life! Please know there is HOPE to beating MS, no matter what your Dr's are telling you! There is overwhelming evidence as to how alternatives can heal us! Good Luck! To our health!
He is a very decent person. Bless his heart.
Which alternatives worked for you?
nice personal appeal
I Hate this disease, I would never wish it on anyone !
Jack Osborne has become a wonderful human being !! Love you jack !! Not to bring the vibe down but my mom died at 34 of MS and was completely blind at 29 and my aunte has MS 2 and now I'm going for more testing after my Hoskins lymphoma after chemotherapy and radiation they saw white matter in my brain which could be from chemo but they need more tests to make sure.. my mom committed suicide by putting a gun in her mouth but I will fight whatever comes my way !!!
Jack looks like Carson daily mixed with Russell Crowe
I hate MS
No money in the cure...sorry
Why keep quiet about the stem cell treatment you had? If it helped you why not bring that to our attention? That would help people with MS more than just awareness.
I didn't know he has HSCT which has a 90% success rate. I'm signed up to go in July but the cost is insane.
Multiple sclerosis is an illness that I wonder if it will go away just the same way it came. But I trust Jesus will heal us.