My Multiple Sclerosis Diagnosis | MS Journey | MS Story | Multiple Sclerosis Symptoms

2 years on and I’m so incredibly proud of this young man I have the privilege of calling my son. This video just came up on my feed again and it reminded me of where we were two years ago. Incredible mental and physical strength meaning for a more than normal life now. Well done buddy boy. Love you❤️

I’ve been having symptoms since 6-8 years old and family dismissed it. I am now 24 years old and symptoms are far far worse. Finally taking a stand and demanding answers. Nerve conduction test in a few weeks. Definitely a nervous system issue I have leg convulsions and tremors and all signs point to MS but we shall see. I’m scared but ready to get answers to get treated. I deserve this. Who disliked this, I’m SO grateful you shared your story!! Fight on

I had to pay for my MRI because the insurance company thought i should go to therapy first! Diagnosed January 2023 at 55! 😢 fighting it every day because MS didn't know who she was dealing with!! ❤❤😊I'll be honored to take this journey with you!

Thank you for sharing your journey on MS . My husband is 69 and his MRI indicates that he has MS. He has a neurological appointment within the next few weeks. Take care and God bless you with healing and wisdom on your journey ❤

Thank you for making this! I’m going through this now. 6 years ago I thought I had MS and my MRI came back normal, here I am 6 years later with lots of symptoms one including a numb foot for 2 months. I hate to hear you’re going through this but I feel less alone.

Inspiring. I admire your positivity and strength Mr Tom Garbett. Keep on helping others with your videos, your helping to change other people’s lives like you have had to change yours. Amazing.

Thanks so much for sharing your journey with MS. I have non-MS demyelination and a very similar picture of symptoms; the first major one being when I stepped on a long nail which almost disappeared into my heel and no pain… totally numb! I’d been experiencing intermittent loss of sensation, foot drag etc but shrugged it off and kept going. The vision, balance problems were extremely gradual and sporadic. I have had remissions lasting a year or more until recently, which have allowed me to look after my kids and my mother, thankfully. I’m no longer able to walk more than a few yards and I can’t face any more drug treatment which hasn’t helped. So I’m grateful for anything nutritional and supplements advice you find beneficial. Many, many thanks for sharing yourself and enjoy your day. 🙏🏽

Thanks for posting, Tom. Be the best you can be.

Thank you for sharing your story

Been dealing with monster for 25 years I'm still mobile but need a cane now. Stay positive

Really informative video, Tom. Thank you.

You are a warrior mate! Stay Strong

Sending you all the love brother. We’re all in this together. No one fights alone 🧡

Clear concise inspirational vid appreciate your insight, waiting on some results to see if I have Ms or not hoping for the best I’m ready to battle either way !

Hi Tom! Just found your video and it resonated a lot with me. I was just diagnosed with MS (less than a month ago) and, just like you, I kinda had been expecting it for the past 2 years. And also like you, I am 27 by the time of the diagnosis. Even though MS is not a good thing, for me, this is the biggest of motivations to get healthy like I have never been before, for sure. 💪 Thank you for your video! Will subscribe 🙌

Half the battle is your attitude, so you defiantly got a good one! You will do well🙏🙏🙏

We share very similar experiences. I'm currently in a clinical trial for Ocrevus, fingers crossed. Wish you all the best bro, stay strong!

Thank you so much for making this Tom! Really helped me to hear this as I'm currently struggling tremendously with my symptoms which have just flared up for the first time. As a 19 year old university student it has been recently been completely destructive towards my academic, social and personal life, experiencing symptoms which doctors have told me point towards MS. So I'm starting to realize how frustrating it is to be held waiting for months if not years for imaging and consultations in order to get a diagnosis. Wishing all those suffering from demyelinating diseases utmost health, awareness and mental fortitude❤️🙏

Thank you for sharing. Love the positive thoughts it’s so so important. I’m going through tests for mg or ms. I seem to have symptoms from both and I don’t know where I sit. All the best.

Hi guys, I'm also diagnosed with MS at the age of 27 too, my left aide was strange for. 3-4 months after a physiotherapy i went to neurologist and diagnosed with MS.