Sorry it's taking me so long to come back and reply to comments. TBH it's been very emotional (in a great way), and I needed time to get myself together to go through the comments. I'm met with gratitude and joy that God blessed me with such an amazing community. Words can't express how thankful I am for all your uplifting prayers, the success stories of you guys dealing w/ MS and the health suggestions overall. My family and I appreciate you all, and I can't wait to connect with you all again later down the road. I started treatment already, and I have already began a new diet and added exercise to the mix. I feel myself doing much better everyday, but I'm also taking my time as well. Just want to broadly thank everyone again. I love ya'll for real. ANDDDDD AS ALWAYS NINJASSSSS, I GOT THE SLICE, GLORY GOT THE RICE - HA HA HAHA HA ✌🏽 - Matt
I am so very sorry! As a chronic pain sufferer, I have CRPS and Acute Hepatic Porphyria, it is so important to stay positive mindset. You’ll quickly find that being an advocate for yourself and your care. It’s rough but thankfully there are treatments. You and your family are in my prayers.
I've been watching you guys since day one and to see you in this state, my heart goes out to you. No one should go through this. I pray God heals your spirit. I love you guys and hope and pray you get through this, Matt ❤ You're strong 🙏🏼
I was diagnosed with RRMS 20 years ago, I had symptoms since I was a teenager. Long story short, I ended up waking with a cane, unable to remember how to drive at one point. The best thing I did for myself was to eat for my health. I have been in remission for 18 years now just from eating organic, homemade, diet. Research shows a Mediterranean diet is excellent for MS, you can do further research into that and you will find the studies and research. Omega 3’s help to repair. Trust me, you don’t need to be scared if you get into remission. Blessing to you Matt. Take it easy. Relaxation helps a lot. Also going into ketosis is beneficial to recovery as well. And don’t listen to them saying you aren’t going to be at your best. Do yourself a favor and look up success stories of even the most advanced cases and keep moving forward. You’ve got this.
I think vitamin d supplementation would be good as well ....me an him are around the same skin tone so I can tell he rarely gets any sun ...an us black folk need way more vitamin d than the average person due to more melanin....vitamin d is huge in the immune system and inflammation department
Matt you have a strong faith in Our Creator, our Holy Father, please listen to this mannnnnn & above else keep God FIRST! GO HARD I SWEAR YOU GOT THIS! YOU ARE COVERED IN THE BLOOD OF CHRIST YOU ARE UN TOUCHABLE! YOU HAVE AUTHORITY LETS GET IT ! THIS IS NOT YOUR CROSS ! ✝️🔥🕊️🫶🏽
Matt,my husband was diagnosed with MS over 10 years ago and with proper diet and exercise, he lives a relatively normal life. You need to take care of yourself. Pushing yourself too hard will only make you worse. Your videos don't always have to be funny and happy. You and glory are REAL. That is why we all love you. Share whatever you want and we'll watch!
@@Stefunny-e6q My partner has MS and when it comes to exercise, he goes to the gym twice a week. That way he gets the training he needs to ease his back pain without overdoing it. We also go for a walk every weekend. When it comes to diet, that is my job, since I am the one who cooks. I try to make meat dishes twice - third times a week, with a lot of veggies, and the rest are vegetarian dishes. And I cook with less oil. That is something that I grew up with, my mum has always cooked with less oil. That is what we do, but at the end, you have to find it out for yourself what works for you.
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclipsMay God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Today I tested positive for ALS after having a horrible hard times, and feel the same way you described in your interview. Listening to you share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤❤
Thank you for this tip it’s also a double win for me because binge watching them is like a therapy ❤️ let’s pray for them and help them reach out to more audience, they deserve so much more!
I was diagnosed 20 yrs ago. It's definitely scary & overwhelming at first. The brain fog & fatigue are my worse symptoms but I've had more goods days than bad ones. Still working over 40 hrs a week. Im on occrevus 2x a yr. That's what I could commit to. Recently, my neurologist said some of my brain lessions have disappeared. Which is amazing.. you got this!!
@@lydializ2705how are you dealing with ocrevus? I am currently on Tectidera and my neurologist has suggested switching to Rituxan (kind of like Ocrevus) But I feel like I can’t decide whether or not to switch I am scared of becoming even more inmune compromised.
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤
Wow. That hit hard. On some level, I can relate. I was diagnosed with cancer just this week. No family history, out of the clear, blue sky. So many people, family, friends, coworkers, have reached out to say they're praying for me. It does feel amazing to hear that. So, let me say this, I am praying for you and your family. ❤
Sending prayers for healing, strength and so much love. With God all things are possible through he who strengthens us. I pray it was caught early and that you beat this! You’ve got this. 🥹🥹🤎🤎
”Do not be anxious about anything, but in every situation, by prayer and petition, with thanksgiving, present your requests to God. And the peace of God, which transcends all understanding, will guard your hearts and your minds in Christ Jesus.“ - Philippians 4:6-7 🙏🙏🙏thank you for sharing with us. Continue to put your faith and hope in the Lord during the valleys. God’s got you!
My 1st diagnosed with MS, I was 26 yrs old with my twins at 1 year old. 1 . Was paralyzed from my waist down. 2. Then, lose sensations in my hands, neck 3. Lose my sight (just saw an outline of people and things) 4. Lost my balance Taken medications and once did IVv treatments. I have been in remission since 1995 with no medications. Fatigue and mood is a big one that I dealt with. You have to try and live a stress free life as one of MS triggers is stress. I didn't miss work much and drove during my years of MS I am now 63 and going strong. With God all things are possible.
My grandma was diagnosed when she was in her thirties. She lived to be 98. She had a happy life and was very happy. As long as you surround yourself with people who truly love and care for you. You’ll be fine!
@@FullyLovingYourself my mom has had it for almost 30 years now. Physical therapy and assistance is key. It won't be immediate, but responsibilities may shift. My mom had to stop driving completely by year 4. There has been advancement in treatment and if they had now what they had back then, my mom might be a little better off. She's 70+ and even pneumonia from covid didn't take her out.
People sometimes criticise Glory for 'doing the most' or whatever but, in this video, knowing she's sitting at the back and letting Matt get through his story the way he intends, supporting him silently, and with what he's shared about what she does for him and the family without publicising it or asking for credit... Man, Glory's the best. Lots of love to you Matt, and you too Glory x
Glory is amazing!! We've been going through this together and if it wasn't for her Idk where I would be physically and emotionally. One of my biggest prayers is that God blesses her w/ more than she can imagine because she honestly deserves it. She doesn't complain, always wants to help and is always smiling even through the rough times. I love her so much ❤-Matt
Glory is amazing and you’re amazing 🥲 from the moment I seen your videos I was glued to the both of you! My girls are grown now and at times miss them not being home. Your videos bring that spark back to my life. Honestly my heart broke hearing you talk about your diagnose with MS. I grew up with my dad having MS and he pushed and tried very hard to make his life as normal as possible for us! He was a man of faith and thinking positive! Prayers to you ❤
I have had a diagnosis of RRMS for 20 years. I also live within 2 hrs of Baltimore. If you need friends or to talk about it let me know know man! Prayers!
.Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo.
Matt (slice), I have a book of prayer that I have been keeping for years. I will be adding you to this book because I pray for everyone in my book everyday. I will also be adding Glory for continued strength and live in helping you. Love to you both.
I saw the title and started crying. I have Lupus and melanoma. God will bless you, your family and give you the strength to bring you through this. My prayers for you and your family coming from my family. 🙏
Matt, my heart goes out to you. In 2020 I was diagnosed with NMO which is a sister of MS but more severe. I've been blinded in 1 eye and semi paralyzed needing a cane and grocery shopping with an electric cart. By the grace of God through faith, I regained 90% of my vision back and I got my mobility back. I've been IV medication for 3 yrs and has been relaspe free. God has been so good. Hold onto your faith. Your story will inspire so many people. God will use you beyond measures. You're in good hands. If God is for you, who can stand against you? Blessings Brother.
WRONG INFORMATION MS is more severe ℹ️ because with NMO it often affects only the optic nerves and spinal cord but with MS Lesions occur in the brain as well as the spinal cord & optic nerves.
I have Neurological problems too but have been refusing to see my doc for over a year (scared of the diagnosis). This video has given me the encouragement I need to go back and be seen and face the answers I fear I'll hear. Thank you for inspiring me, Matt, and best of luck in your future!
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
@@Holly.Brewer I think you mistakenly replied to me in your post LOL. But I'm very happy for your negative diagnosis and am praying for your continued good health.
I’m literally wearing my Slice n Rice hoodie omw home from the gym in tears rn. This channel has been such a light to me and you’ve been through so much recently, bro. I’m praying and believing for complete healing in every area of your life, in Jesus name 🙏🏽
Hi Matt, fellow MS warrior here, diagnosed in 2021!👋🏾. I've been a fan for almost a decade. I just want to let you know that it's ok to grieve for the old you and your future you. It's okay to be sad. All hope is not lost. There will be really good days and really bad days. Those who dont have MS really don't get how debilitating the fatigue can truly be. It may take a while with this new diagnosis to find your footing, but you will eventually find your way back to yourself. Take it a little bit at a time. New advancements are being made all time, and the trajectory of the disease is not what it once was. Keep the faith and lean on Glory and your beautiful sons when it seems all hope is lost. You've got this!!! I can't wait to see what's in store for you next!
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
I was diagnosed with RRMS 11 years ago. Life will be challenging. It can be hard to stay positive, but finding reasons to smile every day has helped me get through the hard days. You've got this. 🤗
First and foremost, thank you for sharing. Matt, you didn't have to share your diagnosis in detail with us, but you did. Sharing your experience and testimony will not be in vain, because when you're young you don't think something like this could happen to you. Someone is going to hear this and get themselves checked out or advocate for further testing from their doctor. Praying for you and Glory and the boys as you all go through this journey. It is a journey, not only for you , but for everyone that loves and cares for you. I see you haven't lost your sense or humor. Keep that, it will serve you well when some days are just a bit too much. Sending all of you much love and prayers.
Thank you for this comment, I couldn’t have said it any better. I’ve been dealing with back issues for some time and have had issues but put them in the backburner and have tried to push through them. This video made me feel emotional, is def making me consider looking into my back health again. Thank you Matt for sharing 🙏🤍
@torresguzman94 Life sometimes gets away from us that we forget to take care of ourselves. Please see a doctor about your back and make sure to advocate for yourself. I've been their too many times when a doctor doesn't always listen. You know your body. Praying for you.
As a PA who specializes in multiple sclerosis, I understand how difficult this diagnosis can be. I’m glad that you got on treatment, and you are on one of the best medications. You got this!! ❤️
Man, I was watching this and at one point I thought “man this guy seems like a Christian” and then he said “I’ve been reading the Bible more and praying more”, and I was like awe yay! It’s so nice to find other brothers and sisters and be reminded that we are all going through something
God is a healer, By His stripes we are healed...We love you Matt, my brother in Christ! Trust in the Lord, no matter what anyone says. He has the final word. We will be praying for you and the kids!
@@SomeFrenchDudeFirst it's obvious that you have no knowledge and no relationship with God. Fortunately for you, God is forgiving enough to give you time to repent from this bogus lie you are spreading. Jesus came to give life and give it to the full, focus on that..Read your Bible and learn about who God really is .
@@SomeFrenchDude So sorry that you don't understand this. I pray God will touch your heart and mind at some point and you get knowledge and understanding. Peace and blessings in Jesus name I pray
@@SomeFrenchDudethis isn’t Gods doing it’s an attack of the devil happens all the time to everyone and especially believers to test our faith in God this is a Christian channel try to be respectful even if you don’t believe ❤
Literally wept after I watched this video. Especially as a scientist, I am soo motivated every time I hear stories like yours to work even harder towards cures for these diseases. Matt just know that your followers are all praying so hard for you. I hope every day you feel our love and support and it comforts you. You and Glory have got this!
My sister was diagnosed with MS when she was 18, and has been living with it for the past 20 years. She has spots on her brain & spinal cord, but her relapses have thankfully been more mild. Her symptoms started with her eyes, but during relapses she would get tingles in her arms/legs and her vision would blur more. She deals with MS fatigue daily and brain fog, but she can still walk without a walker or cane. She presents as someone who has an “invisible disability” which can be hard because she looks like a typical 38 y/o, but really deals with this chronic disease underneath the surface. About 4ish years ago, she started IV medication and some of her spots/lesions have gotten smaller! I hope this will be the case for you too. Sending love & good thoughts to your family & you!
Hi Matt, it feels weird to care so much about a stranger who doesn't even know of my existence, but I guess that's what a parasocial friendship feels like. It really shook me to the core to hear about your diagnosis! You and Glory have grown to my heart since the early days when you started making couples videos! And I'm sure I'm not the only one who cares so strongly about you guys! There's probably at least THOUSANDS right now, coming together before God praying deeply for you! "For where two or three are gathered in my name, there am I among them.” Matthew 18,20 There's probably an ARMY of prayer warriors out there right now, of whose existence you don't even know. Just remember that! I love you guys so much and keep praying for you!!
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips...
I was just diagnosed with MS today 😖relatively new to it too, this video helped me understand it a bit more… im a 26 year old woman , and I really wanna say.. hearing you be open about this really helped me kind of ease my mind to know im not alone . Thank you for this video and i send prayers your way! we will fight this !
We will get through this ❤️ I’m doing much better and more confident that it will not define my path moving forward. I’m more aware of myself better than ever. Sending prayers to you!
I pray all is going well for you. Hang in there, stay positive & stay active! You’re young & you have your entire life waiting on you to live it to your fullest!! Blessings from Texas 🤗.
I was diagnosed with MS in 2006. I had to retire from teaching because I went from 3 lesions on my brain to being fulled of lesions. Once I stop working the progression slowed completely down. God is how I get through this and prayer. I still drive, walk, and love being a wife and mom to 3 . Believe that by His stripes you are healed. I will pray for you and your family . Nothing is too hard for God. I’m living proof that miracles still happen.
I'm sorry you are going through this. I was diagnosed with Neuromyolitis Optica spectrum disorder. It is very similar to MS. They are in the same family. My spine and my eyes are affected, specifically my right eye, which is now blind. I've been in remission from it for over 10 years. I was diagnosed with Systemic Lupus Erythematosus at the same time as the NMOSD. You're not alone it's life changing, but I've learned to pace myself, find my quiet places, eat better, and stay focused on my relationship with God. Stay in the word and in prayer. God's got this. Be blessed.
Hi Matt, I appreciate it has taken a lot to make this video. I am a doctor and whenever I see patients with MS, I see the impact it has on the whole family. Prayers with you all ❤
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
@@slicenrice I pray you get through this Matt I heard your story wishing you well and want you to get through this it sucks I know that you’ll get back on your feet and connect with us all!!!
This is crazy I feel like the universe is giving me hope. Ive had multiple of my favorite youtubers either mention, donate or in your case say they have multiple sclerosis. I have had half my body (mostly affected my face) go numb or the nerves go haywire and twitch. Ive gone temporarily blind. So many crazy symptoms. Took me a long time to get diagnosed. I got diagnosed very young too at 22 years old but dealt with symptoms for a long time. I was so stressed and telling myself I was just lazy and needed to push harder. That was not the answer, I lost chunks of my hair from the stress on my body. Ive also been on that crazy rollercoaster of emotions. Ranging from euphoria to deep turmoil. Memory loss (I thought I was losing my mind). Spasms and numbness. Extreme heat intolerance. I also had phantom smells and weird deja vu. I deal with a lot of nerve pain as well, hand eye coordination, weakness . It helps a lot when I see others coming out with their diagnoses, although I wish you weren't going through it. It just helps me feel less alone in my journey with this illness. I was scared when I got diagnosed but also incredibly relieved because I went so long thinking I was just a worthless pos, lazy, a complainer, not enough willpower and strength. I also was grateful it could be treated and not necessarily a death sentence. I also agree with the fatigue. It comes on so strong and fast. Thats the one thing I find hardest having 3 young kids and limited energy. You guys are amazing and Im here for both of you. ❤ I relate so much and you dont know how much this has helped me.
I can see the sadness in his eyes 😞 i wish you recovery and strong mental health to deal with all this going on. You have a beautiful family that will always be by your side❤
😊Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤
I was diagnosed with MS at the age of 22 . I went to the hospital because i had lost vision in one of my eyes. turns out i had an optic neuritis. They did an MRI and found sclerosis in my brain. I was so scared. Started with self injections for the first 3 years.. didn't go that well, so they put me on IV treatment instead. I've been on Tysabri for the last 7 years and my MS hasn't progress one bit! so there is hope. You got this!
...May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Dear God, please be with Matt and everyone dealing with any illness. Heal Matt and grant him many more years to take care of his family and see his kids grow. We love you Matt and will continue to pray for you. Trust in the Lord. He's got you. Glory, God's got you and your family. I pray that you grow old together no matter what. Your love story inspires me so much. I'm 35 and single because I refuse to settle for anything that God isn't blessing. But seeing love stories like yours gives me hope that I will meet a man who will truly love me and with whom I'll grow old. Cheers.
Hey buddy, first off let me say that I'm sorry to hear about your diagnosis. I was diagnosed with Relapsing Remitting Multiple Sclerosis in 2020 and I want you to know that you will be alright. A good balance of diet, exercise, and regular medicinal treatment is your best bet. My neurologist told me that with all of the research, medication, and everything that we know about MS now, there's never been a better time for those of us with it. You aren't alone. You'll be alright. 🙏🏽
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo😊😊
I was diagnosed in September after partially losing my vision in one eye. My vision has been completely restored and I am so grateful. I am slowly learning what triggers my symptoms or helps relieve them. I definitely forget at times, and it takes time for me to process like I use to. I've learned it happens when I am doing too much at once. Cutting things out of my life that I can deal without and readjusting has been helpful. I believe that God is a healer and praying for your healing as you are on treatment.
..,May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips😊
Matt! My dad has had MS since I was 13! I’m 26 now and he’s doing well and just turned 69 on Valentine’s Day! We all have so much faith in you, you are gonna rock this new chapter in your life. We’re all rooting for you! ❤️❤️
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo..
I also have Multiple Sclerosis. Getting that diagnose was devastating at first but you get used to the idea that MS is just as unpredictable as life it self. I also uploaded a video to my MS story if that helps! I wish you the best Matt!
Hi slice I was diagnosed with MS as well when I was 26 years old I am now 31 . It’s tough at times and it’s also frustrating when I feel like I can’t control my body . I will pray for you because I know how hard it can be !
It sucks. I have RA. It's not the same but we are all going through the same thing..... out temples, bodies are betraying us and we can't do anything to stop it.😢
.Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo..
I had a ischemic stroke at 21 years old. I went from playing basketball to being confined to a hospital bed for a month. Since then I haven’t been able to live life like I want to. So I feel you 100 percent. You have my prayers and my sympathy. I love you man. You guys brought a lot of joy during my life at that time.
I was diagnosed going on almost 11 years. It took them about 3 years to finally get a diagnosis. Super scary at first I went through all kinds of crazy thoughts and emotions. The way medicine has gotten so much better and things have developed so much you can live your life with some obstacles but it isn't life ending. Stay strong and have faith.
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips❤❤❤.
Hi Matt, I know you will get lots of responses and support for this video. As Black female, healthcare provider, and a person with immune issues… I hear you and I want you to know that you are not alone! In this life, we are given assignments to confirm our strength in the lord… a higher power. Lean on your faith, family and the wisdom to know that God has your problem in control… it’s being worked out right now! Do not stop being… do not stop doing things that bring you joy, and whatever you do… don’t worry(I know that hard to do sometimes, but stress is not good). I never post anything, but it was put on my heart to reach out to you. I am praying for you and your family because you are blessed and highly favored! Stay strong 🙏🏽 ❤
I was diagnosed with multiple sclerosis at 21, I am 25 now. I have ADHD and MS. I did not know what MS was before I got it, I remember telling my school healthcare that I walk from my room to kitchen and I feel like I went for a jog, they laughed and said even 85 years old don’t have that. I felt embarrassed. Me and my mom went to gym together and my mom said how can you be more tired than me everytime? I remember after MRI and getting diagnosed with MS and spending a whole month in hospital, I asked thenurse 3 times and said I get better right how long till I feel better, or does it go away and thought to myself how rude of them, now I know why they ignored that question. The day I was planning to go out with my friends and all of sudden right in the call with my friend I got so dizzy I had to stop the call and could not stand, which I believe stopped me from going, thank God. I believed it was unfair and hated God and felt like why me, I know I hate for saying this and I cry still, but I needed it, God had a better plan for me, and knows me better that this was the best way to protect me, because nothing else would have stopped me from not going. This slowed me down with my ADHD, and I took better care of my health and will never take it for granted every since. I have watched you and your wife before you had a baby❤️ You guys always made me happy, thank you for that. I know MS can be very hard with its cognitive side and physical side, for that reason when you have people you love beside you who understand and believe you, it will make you feel better. With MS it is an disease that is hidden, because you are not missing any body parts, but you have it. I wish you all the best and stay strong🦾 Your baby needs a superhero dad🫶🏼 BTW GOOD NEWS! I was pescatarian for 4 years, starting meat my lesions got smaller in my new MRI scan. Nobody told me they can get smaller so let’s fight this together meat is not “unhealthy” sorry vegans, fight the matrix, no more veganism and more carnivore😮💨Remember you might have MS, but that just means the game called life that we all playing right now, we just have it on hardcore GOD mode difficulty, we are not weak the game difficulty is next lvl bro😂 Hahah God bless you!
Speaking supernatural healing over you in the name of Jesus, from your sis in Wellington, New Zealand. Much love and blessings to you and Glory and the babies. Keep moving in faith 🩵
I was diagnosed with MS 2 years ago! I exercise and try to eat the best I can. I have not had any major flare ups since my diagnosis and no new lesions have been found. You got this! Definitely shakes you up a bit but continue to live. Thank you for sharing your story and continue to surround yourself with love and support. I will keep you in my prayers. 🧡
I was diagnosed with MS in 2018. Won’t lie, when I just got the results and being in the healthcare industry, I fell into a depression. My family , church mentors and friends pulled me through. And my mom being a physician herself, completely helped me change my eating habits (juicing anti inflammatory fruits and veggies) and incorporated yoga for MS into my daily exercise routine. And it’s been a game changer. I haven’t had a new lesion since being diagnosed. And I thank God all mighty for that. I surprise my Neurologist every single time. Praying for you and your journey in Jesus name 🙏🏾❤️
We love you Slice. I love your energy and your positivity energy, and I’m glad you have your loving family support. You’ll go through this as a champion ❤
Oh my gosh!! When I saw this notification, I clicked soo fast. I have RRMS as well and I was diagnosed in 2017. Multiple sclerosis is a very scary and difficult disease to deal with, but you got this! I currently take, Ocrevus and it helps me soo much and maybe it can help you as well because everything you said in this video is literally what I deal with! Just say “I have MS and I’m not going to let it control me“ ✊🏾💯🔥
they thought i had cancer for a few months. couldn’t figure anything out, but with the right doctors, right support, and right medication it’ll help. if you don’t want to do the IV medicine ask about Kesimpta! I’m on that and it’s a once a month self injected needle pen. i still struggle a lot with symptoms sometimes, especially when getting hot! it’s important to try to stay cool and LISTEN TO YOUR BODY. if your body tells you to rest then REST. you’ll get through it. I’m only 24 and i never imagined this would happen to me. i feel your pain.
Hi Matt, I Was Diagnosed in my 20s with MS, and I've been living with multiple sclerosis and have secondary progressive in a wheelchair, and Slowly losing Going blind. but I work hard every day they, it's not easy. I tried to go to the gym.I try to socialize with family and there is MS groups out there to help you if you need it.I am a warrior.Never give up, no matter what..We all pray.❤
@jaredgable390 Not everybody goes through the same things. It just depends on if you're on the right medications. Or taking care of yourself. Their days , it will be hard but you don't Give up on yourself. No matter what..
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
I watched every ad in this video. I will continue to watch EVERY video and watch ALL of the ads for support. As well as send prayers for healing 🙌🏼 God bless your family 🤍
.Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo🎉
My cousin has the same type of MS and she did HSCT treatment in Mexico 8 years ago (we live in Australia) and it completely halted her MS. She got the treatment a couple of years after first being diagnosed. She’s had no more relapses and doesn’t take any medications anymore either. Apparently it doesn’t work for everyone but since you are newly diagnosed I think it would be worth looking into! She has a fb page documenting her HSCT journey and still does yearly updates on her anniversary of her new birthday as she likes to call it 😊 Happy to share if you’re interested.
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
I've had an autoimmune disease for almost twenty years. Eating wholesome foods is an absolute must--it has helped my condition tremendously. I never eat processed foods, dairy and added sugar. Best of luck to you and family.
You're a breath of fresh air homie. I'm a black and have been in Cali for the past 2 years and I still look strong like bull, but I walk with a walker, and there's not a lot of people that look like me around here, so i feel that people, subtly view me as a con man, just a lazy con man. Then I think of Muhammed Ali, when he said,"I'ma show you, how great I am". So I'm knuckling up with this. I see the neurologist soon and up to right now here in Cali, the doc brought up possible NMO and in Florida, a couple of years ago, brought up possible MS. Whatever it is I've gotten drastically worse...so it's good to see someone that looks like me, talking about this. I'll pray for you and your fam, that y'all will be valiant. Stay up homie, you got this, and whatever I got, one thing is for sure, I got this...so may we fight, like there is no tomorrow...I was born for this , word up😊
The first 6 months of an MS diagnosis I think is the hardest (it was the hardest for me). But, I'm proud to say I've been on my IV medication for over 4 years and I've had no new lesions. I wish there was more of a community for us out here too. Especially us younger folk. It's hard having these discussions with people who aren't facing similar day to days.
My grandma was diagnosed when she was 21!! She lived a long fulfilling life. She passed away in May 2023 at the beautiful age of 69. I love that lady to pieces!! Everyone who knew her did. She was the mom/ grandma of our neighborhood.
My wife got diagnosed with MS in 2018. It truly has been life changing especially because we wanted kids. She has been taking the weakest MS medication because that's the only one that's safe for pregnancy. Now we have 2 kids and we couldn't be happier. It's not easy, but people like you and my wife are the strongest humans out there.
I didn't think a video on RUclips could make me cry, damn. I'm sorry for what you're going through, Matt, it must feel scary and overwhelming. But you're an amazing and strong individual, and I wholeheartedly hope that this condition won't impact your life too negatively. I'm happy that you have Glory by your side, there's no doubt in my mind that she loves you unconditionally and will support you through this. And thank you so, so much for sharing this with us. Whatever you do, don't deal with it alone. Keep being honest and ask for a helping hand when you need it. I love y'all, take care of yourselves and each other.
I just wanted to say that If you have suicidal thoughts or mental trauma or even if you don’t or just going through a thought time or neither just know that I love you and your loved by many and people and if you think that might not be loved by your family or people you know or just anyone just know they might even love you even more than your think. You have a purpose you are beautiful, kind, just be yourself and go after what you want to do. You are amazing, you got this, and things will get better in your life, you will do great things, and so many people and I are proud of you. Your future is bigger than your past and your past does not define you are awesome and a warrior. Don’t hate yourself simply because of your past, forgive yourself, love yourself no matter what because you deserve the world and the great things in it. I love you Have a wonderful beautiful nice day. Also how are you and your family doing today? Hope you feel better and your family.❤️ Be yourself no matter what you are, have, or what to be you are still amazing and you kind and beautiful always you are the light of the world. Stay safe. 💪🏽❤️. Have a beautiful day.💯❤️❤️💪🏽
Doctors just tell us what to go to God about!!! You must not give in to illness. Your boys and Glory need you. You need you! And you deserve the joys of life. You have to make up your mind that you’re gonna seek Joy and live happy and do and see as much as you can. Even on your sickest and worst physically challenging days you have to keep your hope, continue to seek Joy and hold on to your faith. Believe God and pray for him to allow you to know him personally as HEALER. I ask God to return your faithfulness with more and more grace.
Bro!! As a believer I am standing in prayer with you! My wife and I have love popping in and seeing your families journey over the years!! Brother rest in the fact that God holds your future and your family is in his hands! S&R4L!
You haven’t been “you” for a while, so while I am sad/shocked at the news, it’s nice to know what’s been wrong. This makes sense now. If you want to make a video, but don’t feel that you have anything to contribute, please know we are happy to see you both just as you are. Just have as much fun as you can, and we’ll like and comment. Sending prayers your way! Don’t try to make sense of it all. Just give God the glory through it all. Prayers 🙏🏻🙏🏻 Thank you for the update 🙏🏻🙏🏻
Wow, Cousin, my heart dropped when I read the caption of your video. And then I watched. Glad you went to the doctors and got checked out and a second opinion for confirmation. Thank you for sharing. This video may help someone. You, Glory, and those beautiful boys are uplifted in my prayers 🙏🏾🙏🏾 God is healer and way maker. Stay strong in your faith, take care of yourself, and remember God got this and you!!! Love to you and the family 🙏🏾💙🙏🏾
.May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips..💯
Matt, creating this video takes a lot of courage. To be this open and vulnerable about your recent diagnosis just shows how strong you are already. It’s also beautiful knowing how many people are in your corner who care and love you unconditionally. I will be praying for you and your new journey you are about to embark. I have watched you and Glory from the very beginning and will continue to support 😊
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclipsToday I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤❤❤
I hate that you’re going through this. I am so proud of you for going to the doctor and checking up on your health. Luckily, it is multiple sclerosis awareness month. My auntie passed away from it. You are one of my favorite RUclipsrs and I hate that you and your family are going through this. I am praying for y’all.
My son was diagnosed with MS about 3 years ago. He is 34 now. He is doing well with the treatments and working out. It's different for everyone. He had issues with his eyesight and falling from leg weakness. Sending prayers and positive thoughts.
I can't imagine the courage it took to share this information with us. Thank you for your honesty and openness with such a personal matter. Medical diagnoses that change our lives are difficult to process and ultimately accept. You are blessed to have a supportive family to go through this with you and a doting fan base that only wants what's best for you. I pray that you find the path that is right for you and that whatever treatment you choose leads to long-term remission.
I was diagnosed with so many connective tissues diseases. I cried so much because I have a child with severe special needs. All I can think about is him… that keeps me in a dark place but I’m so grateful for my husband and our village. I just pray for him and not me. 😢 that god will guide him and that I will be ok.
To say that this video hit a soft spot for me would be an understatement. 🥺 I was diagnosed with an Autoimmune Disease called Mixed Connective Tissue Disease (MCTD) about a year and half ago. It is a part of the Lupus family which is also seen as an ‘incurable’ disease. For someone who has also been with their lifelong partner since I was 12 (now turning 30 this year), it broke me knowing that this could effect my future with my husband…something we have dreamed about building together since the day we met. It was also really hard coming to terms that something was ‘wrong’ with me with now the whole world seeing me as this fragile being (as if I am made of glass). My immediate family members also didn’t believe my test results or what the doctors were saying because they would state, “well, no one else in our family has this - how could she?!” I went from living a ‘normal’ life by going to the doctor thinking I had a minor kidney infection (not taking any sort of daily medications at that) to being told I have fluid surrounding the lining if both of my lungs, the lining of my heart and my kidneys were leaking protein. I was then admitted into the ER and being wheeled every which way for MRIs, ECHOs, X-Rays while being prescribed 7 different medications (some through IV; some oral) and having my blood drawn multiple times a day as if I was the main source for blood in the whole hospital… It was the most surreal moment of my life…I went through a really depressive time this past year by having to adjust to my new norm of carrying a pill organizer for my morning and night pills and having to see so many specialists every 3 months with bloodwork (some I didn’t even know existed)…if it wasn’t for the blessing of my husband though who vowed to be by my side through sickness AND in health, I wouldn’t of made it this far. I am happy to say that my mind set has changed as I have been in a remission state for almost 6 months now. I have cut my medications from 7 a day to 2 a day for my ‘maintenance medications’ and I feel as though I am getting back to feeling healthy once more (I also switched to a Mediterranean/Vegetarian Diet and have made some adjustments to fit my needs better). PRAISE GOD! I’m typing all of this to say that you are not alone in this autoimmune world and I am so happy that you felt comfortable enough to share this with us. If you or anyone else has read this this far, PLEASE DON’T BE AFRAID TO GET CHECKED OUT BY A DOCTOR! ❤ You truly never know how many people could be walking around with undiagnosed things that are just waiting to be discovered AND cured. God would never put you into a life situation that he knows you could not overcome. Do not let this Diagnosis define you. Bless you, Glory, and your beautiful family.🙏🏽✨
My mom LOVED you guys ! I started watching y’all because of her. She was diagnosed in 2012 when I was 11, and she fought it with everything in her until she passed in 2022. I’m praying for your health and sending love your way. Keep fighting 🧡!
I'm sending you much love❤ my mum has MS and was diagnosed when I was 2 I'm now 24. She's been amazing and I know you will be for your children and wife aswell! Much love 💕
I was diagnosed with MS in 2017, I was 16 at the time and my life got flipped upside down. It's a lot to take in all at once. But God is my healer and I've been calling on him more and I'm doing fine! I hope your journey is steady. I'll be praying for you🙏🏼 been watching you for years 💞
My husband was diagnosed about 5 years ago. With changing his diet( gluten free dairy free no processed sugars etc) it helped him a lot. He actually went to doctor for eye issues too and after long time they found it to be MS and it can be a struggle. Praying for God to help you. It’s a daily battle but God will be with you through it. Take one day at a time and be patient with yourself and it will be better after time. My husband tried the IV at first but changed to diet and it seemed to help him better than the medicine they gave him. However if it works for you please go for it whatever helps. I don’t want to discourage you from medicine but my husband found that diet and exercise helped him more.
I have an autoimmune disease that is sometimes debilitating and really hard to handle. It’s so important for you to go through the grief of the life you thought you’d have and embrace the life you have now. Thank you for sharing. I hope that treatment works well for you and that you can be in remission for as long as possible!! Sending love y’all’s way.
The way I sat here and cried like we're related. Even so, that is a testament to how much I care about you all and I'm so sorry to hear about your diagnosis. I appreciate your bravery and vulnerability to share your story. Even while dealing with MS and the grief, you chose to share in hopes of helping someone else; such a beautiful heart. Love ya'll 💕
I'm dealing with Ms for 6 years. It's hard. No one to talk to. People don't understand me. Hard for me. I know you can do it. Stay up, and take your time. Sending love❤
Wow....wasn't expecting that video... but here we are...Matt, I pray for healing from the inside out! You're gonna get through this! Anytime I need a good laugh, you and Glory are in my rotation of vids I watch. A lot of times, I'll watch multiple videos on the channel at a time! Y'all never fail to make me laugh! Matt, you got this because I know God's got you! Understand that He wouldn't put more on us that we can bear. And I'm waiting for the testimony that's coming from this! And there will be one! Mad love Matt and Glory! From a fellow Baltimore native! Hope to meet y'all one day!
I was diagnosed with RRMS in 2017. It's been a journey. I've been in remission for some time now. Focusing on eating healthy and being as active as I can. Prayers for you. 🙏🏾🙏🏾
Sorry it's taking me so long to come back and reply to comments. TBH it's been very emotional (in a great way), and I needed time to get myself together to go through the comments. I'm met with gratitude and joy that God blessed me with such an amazing community. Words can't express how thankful I am for all your uplifting prayers, the success stories of you guys dealing w/ MS and the health suggestions overall. My family and I appreciate you all, and I can't wait to connect with you all again later down the road. I started treatment already, and I have already began a new diet and added exercise to the mix. I feel myself doing much better everyday, but I'm also taking my time as well. Just want to broadly thank everyone again. I love ya'll for real. ANDDDDD AS ALWAYS NINJASSSSS, I GOT THE SLICE, GLORY GOT THE RICE - HA HA HAHA HA ✌🏽 - Matt
We miss yallllll! 🫶🏽 can’t wait for the comeback, we are rooting and praying for you!
I am so very sorry! As a chronic pain sufferer, I have CRPS and Acute Hepatic Porphyria, it is so important to stay positive mindset. You’ll quickly find that being an advocate for yourself and your care. It’s rough but thankfully there are treatments. You and your family are in my prayers.
I'm praying for you brother 🙏
hope ya feel better bro
I've been watching you guys since day one and to see you in this state, my heart goes out to you. No one should go through this. I pray God heals your spirit. I love you guys and hope and pray you get through this, Matt ❤ You're strong 🙏🏼
I was diagnosed with RRMS 20 years ago, I had symptoms since I was a teenager. Long story short, I ended up waking with a cane, unable to remember how to drive at one point. The best thing I did for myself was to eat for my health. I have been in remission for 18 years now just from eating organic, homemade, diet. Research shows a Mediterranean diet is excellent for MS, you can do further research into that and you will find the studies and research. Omega 3’s help to repair. Trust me, you don’t need to be scared if you get into remission. Blessing to you Matt. Take it easy. Relaxation helps a lot. Also going into ketosis is beneficial to recovery as well. And don’t listen to them saying you aren’t going to be at your best. Do yourself a favor and look up success stories of even the most advanced cases and keep moving forward. You’ve got this.
I think vitamin d supplementation would be good as well ....me an him are around the same skin tone so I can tell he rarely gets any sun ...an us black folk need way more vitamin d than the average person due to more melanin....vitamin d is huge in the immune system and inflammation department
Thank you for sharing.
I hope he sees this ❤
Matt you have a strong faith in Our Creator, our Holy Father, please listen to this mannnnnn & above else keep God FIRST! GO HARD I SWEAR YOU GOT THIS! YOU ARE COVERED IN THE BLOOD OF CHRIST YOU ARE UN TOUCHABLE! YOU HAVE AUTHORITY LETS GET IT ! THIS IS NOT YOUR CROSS ! ✝️🔥🕊️🫶🏽
Likes or not likes look into vitamin d seriously bro there's a lot of research on it , it's going to help you a lot
Matt,my husband was diagnosed with MS over 10 years ago and with proper diet and exercise, he lives a relatively normal life. You need to take care of yourself. Pushing yourself too hard will only make you worse.
Your videos don't always have to be funny and happy. You and glory are REAL. That is why we all love you. Share whatever you want and we'll watch!
@@Stefunny-e6q Trial and error. You slowly start to get acquainted with your body and it's needs.
Diet is overlooked, diet plays a hung part to your overall health
@@Stefunny-e6q My partner has MS and when it comes to exercise, he goes to the gym twice a week. That way he gets the training he needs to ease his back pain without overdoing it. We also go for a walk every weekend. When it comes to diet, that is my job, since I am the one who cooks. I try to make meat dishes twice - third times a week, with a lot of veggies, and the rest are vegetarian dishes. And I cook with less oil. That is something that I grew up with, my mum has always cooked with less oil. That is what we do, but at the end, you have to find it out for yourself what works for you.
This is sooo true and I know they would appreciate this ❤
Montel Williams. He’s been juicing for decades.
My mother has had MS for forty years. She is 72 now. She still drives, walks etc. You are in my prayers. Gods got you.
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclipsMay God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Today I tested positive for ALS after having a horrible hard times, and feel the same way you described in your interview. Listening to you share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤❤
@user-hg1qu4hv2m brother what does he do to not trigger the ms
Community let's help them out and keep them in the algorithm, replay their videos. We are praying for you and Glory.
Thank you for this tip it’s also a double win for me because binge watching them is like a therapy ❤️ let’s pray for them and help them reach out to more audience, they deserve so much more!
Great suggestion! I watched it through once then hit replay and read the comments while it played!
yesss! i kind of stopped watching them for some reason but now i'ma watch em everytime i eat hehe
Yess fully agree!!!!
Yes please
Thanks for this suggestion
I was diagnosed 20 yrs ago. It's definitely scary & overwhelming at first. The brain fog & fatigue are my worse symptoms but I've had more goods days than bad ones. Still working over 40 hrs a week. Im on occrevus 2x a yr. That's what I could commit to. Recently, my neurologist said some of my brain lessions have disappeared. Which is amazing.. you got this!!
that’s beautiful i wish you the best ❤
This is so nice to hear thanks for mentioning this that’s awesome! I was diagnosed 9 years ago and also on ocrevus. I work 40 hrs a week too ❤
@@lydializ2705how are you dealing with ocrevus? I am currently on Tectidera and my neurologist has suggested switching to Rituxan (kind of like Ocrevus)
But I feel like I can’t decide whether or not to switch I am scared of becoming even more inmune compromised.
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Wow. That hit hard. On some level, I can relate. I was diagnosed with cancer just this week. No family history, out of the clear, blue sky. So many people, family, friends, coworkers, have reached out to say they're praying for me. It does feel amazing to hear that. So, let me say this, I am praying for you and your family. ❤
Saying a prayer for you. 🤍
Hun I’m sorry to hear this! I was diagnosed in January with Cancer as well. Praying for Matt and us both!! 😢😢😢
Sending prayers for healing, strength and so much love. With God all things are possible through he who strengthens us. I pray it was caught early and that you beat this! You’ve got this. 🥹🥹🤎🤎
just know that you’re not alone ❤ you’re gonna beat it sis
🙏🏿
”Do not be anxious about anything, but in every situation, by prayer and petition, with thanksgiving, present your requests to God. And the peace of God, which transcends all understanding, will guard your hearts and your minds in Christ Jesus.“ - Philippians 4:6-7
🙏🙏🙏thank you for sharing with us. Continue to put your faith and hope in the Lord during the valleys. God’s got you!
Amen!! 🔥 ❤🕊️
AMEN 🙏🏽
Amen 🩸🙏
In Jesus holy name
Amen❤
My 1st diagnosed with MS, I was 26 yrs old with my twins at 1 year old.
1 . Was paralyzed from my waist down.
2. Then, lose sensations in my hands, neck
3. Lose my sight (just saw an outline of people and things)
4. Lost my balance
Taken medications and once did IVv treatments.
I have been in remission since 1995 with no medications.
Fatigue and mood is a big one that I dealt with.
You have to try and live a stress free life as one of MS triggers is stress.
I didn't miss work much and drove during my years of MS
I am now 63 and going strong.
With God all things are possible.
Great, idk I've MS symptoms but I'm not diagnosed yet, pray for me, I'm 20.
@@JaedenRaine Same too Im 20y old we dont have enough money to get diagnose 😢
@@athleticguts you've got this, just be strong and be happy as much as you can, we don't know when our lives would take a hard turn.
@@JaedenRainei 19
@@JaedenRaine how are you now
My grandma was diagnosed when she was in her thirties. She lived to be 98. She had a happy life and was very happy. As long as you surround yourself with people who truly love and care for you. You’ll be fine!
I love to hear stories of people who are living, surviving and thriving with MS. Thank you for sharing. I’m looking to live like your grandmother
Wow, that's incredible!! My family has been great and honestly they helped this hiccup in my life become really manageable!
What treatments did she do?
@@hibiscusflower5911I’m not sure. I’ll have to ask my dad. I’ll get back to you on that.
@@KanezaMacDid you ask your Dad?
Man, as a child of someone with MS, you got this man. It's not bad news, it's a new chapter
Is your parent living well? My husband was diagnosed with MS we often times wonder about our children
@@FullyLovingYourself my mom has had it for almost 30 years now. Physical therapy and assistance is key. It won't be immediate, but responsibilities may shift. My mom had to stop driving completely by year 4. There has been advancement in treatment and if they had now what they had back then, my mom might be a little better off. She's 70+ and even pneumonia from covid didn't take her out.
Amen, Very true!
Absolutely love your outlook!! ❤
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips❤
People sometimes criticise Glory for 'doing the most' or whatever but, in this video, knowing she's sitting at the back and letting Matt get through his story the way he intends, supporting him silently, and with what he's shared about what she does for him and the family without publicising it or asking for credit... Man, Glory's the best. Lots of love to you Matt, and you too Glory x
Glory is amazing!! We've been going through this together and if it wasn't for her Idk where I would be physically and emotionally. One of my biggest prayers is that God blesses her w/ more than she can imagine because she honestly deserves it. She doesn't complain, always wants to help and is always smiling even through the rough times. I love her so much ❤-Matt
Doing the most? She’s hilarious!
Glory is amazing and you’re amazing 🥲 from the moment I seen your videos I was glued to the both of you! My girls are grown now and at times miss them not being home. Your videos bring that spark back to my life. Honestly my heart broke hearing you talk about your diagnose with MS. I grew up with my dad having MS and he pushed and tried very hard to make his life as normal as possible for us!
He was a man of faith and thinking positive!
Prayers to you ❤
I have had a diagnosis of RRMS for 20 years. I also live within 2 hrs of Baltimore. If you need friends or to talk about it let me know know man! Prayers!
.Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo.
Matt (slice), I have a book of prayer that I have been keeping for years. I will be adding you to this book because I pray for everyone in my book everyday. I will also be adding Glory for continued strength and live in helping you. Love to you both.
God bless you, prayers definitely help. ✝️
I saw the title and started crying. I have Lupus and melanoma. God will bless you, your family and give you the strength to bring you through this. My prayers for you and your family coming from my family. 🙏
God bless you!!! I have Lupus's TWIN SISTER SJOGRENS AND FIBROMYALGIA... BUT GOD!!!! GOD'S GOT US IN HIS HANDS!!!!
Same, I was diagnosed with lupus with mix connective tissue disease a year ago. Prayers for you and for all the loved ones around you
Prayers to you!
I was diagnosed with Lupus SLE stage 4 last December been in and out the hospital ever since.
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips❤
Matt, my heart goes out to you. In 2020 I was diagnosed with NMO which is a sister of MS but more severe. I've been blinded in 1 eye and semi paralyzed needing a cane and grocery shopping with an electric cart. By the grace of God through faith, I regained 90% of my vision back and I got my mobility back. I've been IV medication for 3 yrs and has been relaspe free. God has been so good. Hold onto your faith. Your story will inspire so many people. God will use you beyond measures. You're in good hands. If God is for you, who can stand against you? Blessings Brother.
@infotinav I love this message thank you for posting this positive and motivational message God bless you.
❤❤ God is good
Amen!
Amen!!
WRONG INFORMATION MS is more severe ℹ️ because with NMO it often affects only the optic nerves and spinal cord but with MS Lesions occur in the brain as well as the spinal cord & optic nerves.
NOOO WHAT? my heart DROPPED when i saw the notification
sinked lol
Right!!
Me too :(
Mine did too:(
Me too, heartbreaking honestly
I have Neurological problems too but have been refusing to see my doc for over a year (scared of the diagnosis). This video has given me the encouragement I need to go back and be seen and face the answers I fear I'll hear. Thank you for inspiring me, Matt, and best of luck in your future!
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
@@Holly.Brewer I think you mistakenly replied to me in your post LOL. But I'm very happy for your negative diagnosis and am praying for your continued good health.
I’m literally wearing my Slice n Rice hoodie omw home from the gym in tears rn. This channel has been such a light to me and you’ve been through so much recently, bro. I’m praying and believing for complete healing in every area of your life, in Jesus name 🙏🏽
Amen
..May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Hi Matt, fellow MS warrior here, diagnosed in 2021!👋🏾. I've been a fan for almost a decade. I just want to let you know that it's ok to grieve for the old you and your future you. It's okay to be sad. All hope is not lost. There will be really good days and really bad days. Those who dont have MS really don't get how debilitating the fatigue can truly be. It may take a while with this new diagnosis to find your footing, but you will eventually find your way back to yourself. Take it a little bit at a time. New advancements are being made all time, and the trajectory of the disease is not what it once was. Keep the faith and lean on Glory and your beautiful sons when it seems all hope is lost. You've got this!!! I can't wait to see what's in store for you next!
Praying for you Matt and the family!!
Beautiful comment to our friend Matt...very encouraging ---We luv u Matt!!
Same may of 2021! Rrms. I’m currently on Tysabri and I have had little to no symptoms
Praying for you and you family beautiful family❤.
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
I was diagnosed with RRMS 11 years ago. Life will be challenging. It can be hard to stay positive, but finding reasons to smile every day has helped me get through the hard days. You've got this. 🤗
I pray that God eases your burden so that life isn't as challenging and that you receive a big blessing with your health :)
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
First and foremost, thank you for sharing. Matt, you didn't have to share your diagnosis in detail with us, but you did. Sharing your experience and testimony will not be in vain, because when you're young you don't think something like this could happen to you. Someone is going to hear this and get themselves checked out or advocate for further testing from their doctor.
Praying for you and Glory and the boys as you all go through this journey. It is a journey, not only for you , but for everyone that loves and cares for you. I see you haven't lost your sense or humor. Keep that, it will serve you well when some days are just a bit too much. Sending all of you much love and prayers.
Thank you for this comment, I couldn’t have said it any better. I’ve been dealing with back issues for some time and have had issues but put them in the backburner and have tried to push through them. This video made me feel emotional, is def making me consider looking into my back health again. Thank you Matt for sharing 🙏🤍
@torresguzman94 Life sometimes gets away from us that we forget to take care of ourselves. Please see a doctor about your back and make sure to advocate for yourself. I've been their too many times when a doctor doesn't always listen. You know your body. Praying for you.
As a PA who specializes in multiple sclerosis, I understand how difficult this diagnosis can be. I’m glad that you got on treatment, and you are on one of the best medications. You got this!! ❤️
💯May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Thank you for your profession!!
Man, I was watching this and at one point I thought “man this guy seems like a Christian” and then he said “I’ve been reading the Bible more and praying more”, and I was like awe yay! It’s so nice to find other brothers and sisters and be reminded that we are all going through something
I'm praying for you, Slice. I'm so sorry to hear about this. God bless you.
God is a healer, By His stripes we are healed...We love you Matt, my brother in Christ! Trust in the Lord, no matter what anyone says. He has the final word. We will be praying for you and the kids!
God is so nice that he inflicted him with this condition.
@@SomeFrenchDudeFirst it's obvious that you have no knowledge and no relationship with God. Fortunately for you, God is forgiving enough to give you time to repent from this bogus lie you are spreading. Jesus came to give life and give it to the full, focus on that..Read your Bible and learn about who God really is .
@SomeFrenchDude God doesn't inflict disease though....😮
@@SomeFrenchDude So sorry that you don't understand this. I pray God will touch your heart and mind at some point and you get knowledge and understanding. Peace and blessings in Jesus name I pray
@@SomeFrenchDudethis isn’t Gods doing it’s an attack of the devil happens all the time to everyone and especially believers to test our faith in God this is a Christian channel try to be respectful even if you don’t believe ❤
Hi. I have been living with MS for 20+ yrs. Pressing Forward and taking one day at the time.
Literally wept after I watched this video. Especially as a scientist, I am soo motivated every time I hear stories like yours to work even harder towards cures for these diseases. Matt just know that your followers are all praying so hard for you. I hope every day you feel our love and support and it comforts you. You and Glory have got this!
My sister was diagnosed with MS when she was 18, and has been living with it for the past 20 years. She has spots on her brain & spinal cord, but her relapses have thankfully been more mild. Her symptoms started with her eyes, but during relapses she would get tingles in her arms/legs and her vision would blur more. She deals with MS fatigue daily and brain fog, but she can still walk without a walker or cane. She presents as someone who has an “invisible disability” which can be hard because she looks like a typical 38 y/o, but really deals with this chronic disease underneath the surface. About 4ish years ago, she started IV medication and some of her spots/lesions have gotten smaller! I hope this will be the case for you too. Sending love & good thoughts to your family & you!
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips❤
You are grieving the life you expected to have and like someone wrote "this is a new chapter in you life" wishing you the best.
My mom had RRMS for over 50 years and lived to 80 with very few relapses. I’ll be praying that you have a mild process like my mom. Hang in there ❤
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Hi Matt, it feels weird to care so much about a stranger who doesn't even know of my existence, but I guess that's what a parasocial friendship feels like. It really shook me to the core to hear about your diagnosis! You and Glory have grown to my heart since the early days when you started making couples videos! And I'm sure I'm not the only one who cares so strongly about you guys! There's probably at least THOUSANDS right now, coming together before God praying deeply for you! "For where two or three are gathered in my name, there am I among them.” Matthew 18,20 There's probably an ARMY of prayer warriors out there right now, of whose existence you don't even know. Just remember that! I love you guys so much and keep praying for you!!
Agreed!!! Amen!!!
You said it so perfectly!
This is such a perfect comment!! It said everything I wanted to say.
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips...
I was just diagnosed with MS today 😖relatively new to it too, this video helped me understand it a bit more… im a 26 year old woman , and I really wanna say.. hearing you be open about this really helped me kind of ease my mind to know im not alone . Thank you for this video and i send prayers your way! we will fight this !
We will get through this ❤️ I’m doing much better and more confident that it will not define my path moving forward. I’m more aware of myself better than ever. Sending prayers to you!
I pray all is going well for you. Hang in there, stay positive & stay active! You’re young & you have your entire life waiting on you to live it to your fullest!! Blessings from Texas 🤗.
Stopped in the middle of the video just to pray for you and your family Matt. GOD IS A HEALER ❤.
I was diagnosed with MS in 2006. I had to retire from teaching because I went from 3 lesions on my brain to being fulled of lesions. Once I stop working the progression slowed completely down. God is how I get through this and prayer. I still drive, walk, and love being a wife and mom to 3 . Believe that by His stripes you are healed. I will pray for you and your family . Nothing is too hard for God. I’m living proof that miracles still happen.
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips.
I'm sorry you are going through this. I was diagnosed with Neuromyolitis Optica spectrum disorder. It is very similar to MS. They are in the same family. My spine and my eyes are affected, specifically my right eye, which is now blind. I've been in remission from it for over 10 years. I was diagnosed with Systemic Lupus Erythematosus at the same time as the NMOSD. You're not alone it's life changing, but I've learned to pace myself, find my quiet places, eat better, and stay focused on my relationship with God. Stay in the word and in prayer. God's got this. Be blessed.
Hi Matt, I appreciate it has taken a lot to make this video. I am a doctor and whenever I see patients with MS, I see the impact it has on the whole family. Prayers with you all ❤
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
Sending my love Matt! Thank you so much for taking the time to make the video and update us all. Looking forward to the next time👊
My brother! I appreciate you man, thank you. Hope to run into you again this year for sure 💪🏼
@@slicenrice I pray you get through this Matt I heard your story wishing you well and want you to get through this it sucks I know that you’ll get back on your feet and connect with us all!!!
This is crazy I feel like the universe is giving me hope. Ive had multiple of my favorite youtubers either mention, donate or in your case say they have multiple sclerosis. I have had half my body (mostly affected my face) go numb or the nerves go haywire and twitch. Ive gone temporarily blind. So many crazy symptoms. Took me a long time to get diagnosed. I got diagnosed very young too at 22 years old but dealt with symptoms for a long time. I was so stressed and telling myself I was just lazy and needed to push harder. That was not the answer, I lost chunks of my hair from the stress on my body. Ive also been on that crazy rollercoaster of emotions. Ranging from euphoria to deep turmoil. Memory loss (I thought I was losing my mind). Spasms and numbness. Extreme heat intolerance. I also had phantom smells and weird deja vu. I deal with a lot of nerve pain as well, hand eye coordination, weakness . It helps a lot when I see others coming out with their diagnoses, although I wish you weren't going through it. It just helps me feel less alone in my journey with this illness. I was scared when I got diagnosed but also incredibly relieved because I went so long thinking I was just a worthless pos, lazy, a complainer, not enough willpower and strength. I also was grateful it could be treated and not necessarily a death sentence. I also agree with the fatigue. It comes on so strong and fast. Thats the one thing I find hardest having 3 young kids and limited energy. You guys are amazing and Im here for both of you. ❤ I relate so much and you dont know how much this has helped me.
I can see the sadness in his eyes 😞 i wish you recovery and strong mental health to deal with all this going on. You have a beautiful family that will always be by your side❤
😊Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤
I was diagnosed with MS at the age of 22 . I went to the hospital because i had lost vision in one of my eyes. turns out i had an optic neuritis. They did an MRI and found sclerosis in my brain. I was so scared. Started with self injections for the first 3 years.. didn't go that well, so they put me on IV treatment instead. I've been on Tysabri for the last 7 years and my MS hasn't progress one bit! so there is hope. You got this!
...May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
Dear God, please be with Matt and everyone dealing with any illness. Heal Matt and grant him many more years to take care of his family and see his kids grow. We love you Matt and will continue to pray for you. Trust in the Lord. He's got you. Glory, God's got you and your family. I pray that you grow old together no matter what. Your love story inspires me so much. I'm 35 and single because I refuse to settle for anything that God isn't blessing. But seeing love stories like yours gives me hope that I will meet a man who will truly love me and with whom I'll grow old. Cheers.
Hey buddy, first off let me say that I'm sorry to hear about your diagnosis. I was diagnosed with Relapsing Remitting Multiple Sclerosis in 2020 and I want you to know that you will be alright. A good balance of diet, exercise, and regular medicinal treatment is your best bet. My neurologist told me that with all of the research, medication, and everything that we know about MS now, there's never been a better time for those of us with it. You aren't alone. You'll be alright. 🙏🏽
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo😊😊
I was diagnosed in September after partially losing my vision in one eye. My vision has been completely restored and I am so grateful. I am slowly learning what triggers my symptoms or helps relieve them. I definitely forget at times, and it takes time for me to process like I use to. I've learned it happens when I am doing too much at once. Cutting things out of my life that I can deal without and readjusting has been helpful. I believe that God is a healer and praying for your healing as you are on treatment.
What were the things that triggered you? And the things that helped you? How could you tell?
..,May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips😊
Matt! My dad has had MS since I was 13! I’m 26 now and he’s doing well and just turned 69 on Valentine’s Day! We all have so much faith in you, you are gonna rock this new chapter in your life. We’re all rooting for you! ❤️❤️
.May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
I am sorry to hear that Slice. I will keep you and the family in my prayers. 🙏🏽
My heart dropped when I saw the notification. Hang in there Matt! Praying for you and your family
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo..
I also have Multiple Sclerosis. Getting that diagnose was devastating at first but you get used to the idea that MS is just as unpredictable as life it self. I also uploaded a video to my MS story if that helps! I wish you the best Matt!
Hi slice I was diagnosed with MS as well when I was 26 years old I am now 31 . It’s tough at times and it’s also frustrating when I feel like I can’t control my body . I will pray for you because I know how hard it can be !
Yes it is really frustrating when your body does what it does. It’s also scary because you really don’t know what to expect the next day.💯😭
It sucks. I have RA. It's not the same but we are all going through the same thing..... out temples, bodies are betraying us and we can't do anything to stop it.😢
.Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo..
You have been blessed with a Proverbs 31 woman, I will keep you in my prayers. may God continue to keep you and your family in his rest. 💝💝💝💝💝💝
I had a ischemic stroke at 21 years old. I went from playing basketball to being confined to a hospital bed for a month. Since then I haven’t been able to live life like I want to. So I feel you 100 percent. You have my prayers and my sympathy. I love you man. You guys brought a lot of joy during my life at that time.
This made me emotional i commend your strength and vulnerability
Godspeed and stay with us😊
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips❤❤
I was diagnosed going on almost 11 years. It took them about 3 years to finally get a diagnosis. Super scary at first I went through all kinds of crazy thoughts and emotions. The way medicine has gotten so much better and things have developed so much you can live your life with some obstacles but it isn't life ending. Stay strong and have faith.
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips❤❤❤.
My teenager and 7 year old are watching this and praying for you, Glory, and your kids ❤
I'm so glad you have Glory.
God please hear their prayers.
Hi Matt, I know you will get lots of responses and support for this video. As Black female, healthcare provider, and a person with immune issues… I hear you and I want you to know that you are not alone! In this life, we are given assignments to confirm our strength in the lord… a higher power. Lean on your faith, family and the wisdom to know that God has your problem in control… it’s being worked out right now! Do not stop being… do not stop doing things that bring you joy, and whatever you do… don’t worry(I know that hard to do sometimes, but stress is not good).
I never post anything, but it was put on my heart to reach out to you. I am praying for you and your family because you are blessed and highly favored! Stay strong 🙏🏽 ❤
I was diagnosed with multiple sclerosis at 21, I am 25 now. I have ADHD and MS. I did not know what MS was before I got it, I remember telling my school healthcare that I walk from my room to kitchen and I feel like I went for a jog, they laughed and said even 85 years old don’t have that. I felt embarrassed. Me and my mom went to gym together and my mom said how can you be more tired than me everytime? I remember after MRI and getting diagnosed with MS and spending a whole month in hospital, I asked thenurse 3 times and said I get better right how long till I feel better, or does it go away and thought to myself how rude of them, now I know why they ignored that question. The day I was planning to go out with my friends and all of sudden right in the call with my friend I got so dizzy I had to stop the call and could not stand, which I believe stopped me from going, thank God. I believed it was unfair and hated God and felt like why me, I know I hate for saying this and I cry still, but I needed it, God had a better plan for me, and knows me better that this was the best way to protect me, because nothing else would have stopped me from not going. This slowed me down with my ADHD, and I took better care of my health and will never take it for granted every since. I have watched you and your wife before you had a baby❤️ You guys always made me happy, thank you for that. I know MS can be very hard with its cognitive side and physical side, for that reason when you have people you love beside you who understand and believe you, it will make you feel better. With MS it is an disease that is hidden, because you are not missing any body parts, but you have it. I wish you all the best and stay strong🦾 Your baby needs a superhero dad🫶🏼
BTW GOOD NEWS! I was pescatarian for 4 years, starting meat my lesions got smaller in my new MRI scan. Nobody told me they can get smaller so let’s fight this together meat is not “unhealthy” sorry vegans, fight the matrix, no more veganism and more carnivore😮💨Remember you might have MS, but that just means the game called life that we all playing right now, we just have it on hardcore GOD mode difficulty, we are not weak the game difficulty is next lvl bro😂 Hahah God bless you!
Speaking supernatural healing over you in the name of Jesus, from your sis in Wellington, New Zealand. Much love and blessings to you and Glory and the babies. Keep moving in faith 🩵
GOD is still in control. I'll be keepig you in my prayers.
Amen ! 🙏🏽
I was diagnosed with MS 2 years ago! I exercise and try to eat the best I can. I have not had any major flare ups since my diagnosis and no new lesions have been found. You got this! Definitely shakes you up a bit but continue to live. Thank you for sharing your story and continue to surround yourself with love and support. I will keep you in my prayers. 🧡
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips😊
What medication was you out on?
Do some research with his name Dr ubarlo
@@prettymelanin4870 I take 240mg dimethyl fumarate twice a day
@@prettymelanin4870 Dimethyl Fumarate 240mg
Making a doctors appointment now. Thank you for being vulnerable and honest about this.
I was diagnosed with MS in 2018. Won’t lie, when I just got the results and being in the healthcare industry, I fell into a depression. My family , church mentors and friends pulled me through. And my mom being a physician herself, completely helped me change my eating habits (juicing anti inflammatory fruits and veggies) and incorporated yoga for MS into my daily exercise routine. And it’s been a game changer. I haven’t had a new lesion since being diagnosed. And I thank God all mighty for that. I surprise my Neurologist every single time. Praying for you and your journey in Jesus name 🙏🏾❤️
We love you Slice. I love your energy and your positivity energy, and I’m glad you have your loving family support. You’ll go through this as a champion ❤
Oh my gosh!! When I saw this notification, I clicked soo fast. I have RRMS as well and I was diagnosed in 2017. Multiple sclerosis is a very scary and difficult disease to deal with, but you got this! I currently take, Ocrevus and it helps me soo much and maybe it can help you as well because everything you said in this video is literally what I deal with! Just say “I have MS and I’m not going to let it control me“ ✊🏾💯🔥
i was diagnosed with MS back in September of last year🧡 it’ll get better and easier as you move on.
they thought i had cancer for a few months. couldn’t figure anything out, but with the right doctors, right support, and right medication it’ll help. if you don’t want to do the IV medicine ask about Kesimpta! I’m on that and it’s a once a month self injected needle pen. i still struggle a lot with symptoms sometimes, especially when getting hot! it’s important to try to stay cool and LISTEN TO YOUR BODY. if your body tells you to rest then REST. you’ll get through it. I’m only 24 and i never imagined this would happen to me. i feel your pain.
I pray that you have victory over this ailment! God bless you!
Hi Matt, I Was Diagnosed in my 20s with MS, and I've been living with multiple sclerosis and have secondary progressive in a wheelchair, and Slowly losing Going blind.
but I work hard every day they, it's not easy. I tried to go to the gym.I try to socialize with family and there is MS groups out there to help you if you need it.I am a warrior.Never give up, no matter what..We all pray.❤
Damm is that going to happen to him?
@jaredgable390 Not everybody goes through the same things. It just depends on if you're on the right medications. Or taking care of yourself. Their days , it will be hard but you don't Give up on yourself. No matter what..
Stay focus on being the best you during this time.
You are a warrior! Thank you so much for sharing your life with us. You are teaching us to never give up even when it gets tough!
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
I watched every ad in this video. I will continue to watch EVERY video and watch ALL of the ads for support. As well as send prayers for healing 🙌🏼 God bless your family 🤍
.Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo🎉
Thinking of you and your family! 🙏🏽🙏🏽🙏🏽 Sending prayers your way!! You've got this!!
My cousin has the same type of MS and she did HSCT treatment in Mexico 8 years ago (we live in Australia) and it completely halted her MS. She got the treatment a couple of years after first being diagnosed. She’s had no more relapses and doesn’t take any medications anymore either. Apparently it doesn’t work for everyone but since you are newly diagnosed I think it would be worth looking into! She has a fb page documenting her HSCT journey and still does yearly updates on her anniversary of her new birthday as she likes to call it 😊 Happy to share if you’re interested.
Damn hope he sees this 🤯anything is worth a try imo
Today I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo
I've had an autoimmune disease for almost twenty years. Eating wholesome foods is an absolute must--it has helped my condition tremendously. I never eat processed foods, dairy and added sugar. Best of luck to you and family.
You're a breath of fresh air homie. I'm a black and have been in Cali for the past 2 years and I still look strong like bull, but I walk with a walker, and there's not a lot of people that look like me around here, so i feel that people, subtly view me as a con man, just a lazy con man. Then I think of Muhammed Ali, when he said,"I'ma show you, how great I am". So I'm knuckling up with this. I see the neurologist soon and up to right now here in Cali, the doc brought up possible NMO and in Florida, a couple of years ago, brought up possible MS. Whatever it is I've gotten drastically worse...so it's good to see someone that looks like me, talking about this. I'll pray for you and your fam, that y'all will be valiant. Stay up homie, you got this, and whatever I got, one thing is for sure, I got this...so may we fight, like there is no tomorrow...I was born for this , word up😊
The first 6 months of an MS diagnosis I think is the hardest (it was the hardest for me). But, I'm proud to say I've been on my IV medication for over 4 years and I've had no new lesions. I wish there was more of a community for us out here too. Especially us younger folk. It's hard having these discussions with people who aren't facing similar day to days.
My grandma was diagnosed when she was 21!! She lived a long fulfilling life. She passed away in May 2023 at the beautiful age of 69. I love that lady to pieces!! Everyone who knew her did. She was the mom/ grandma of our neighborhood.
My wife got diagnosed with MS in 2018. It truly has been life changing especially because we wanted kids. She has been taking the weakest MS medication because that's the only one that's safe for pregnancy. Now we have 2 kids and we couldn't be happier. It's not easy, but people like you and my wife are the strongest humans out there.
My husband and I prayed for y’all tonight. God is a healer. Keep clinging to him. God’s got you! 💜💜
I didn't think a video on RUclips could make me cry, damn. I'm sorry for what you're going through, Matt, it must feel scary and overwhelming. But you're an amazing and strong individual, and I wholeheartedly hope that this condition won't impact your life too negatively. I'm happy that you have Glory by your side, there's no doubt in my mind that she loves you unconditionally and will support you through this. And thank you so, so much for sharing this with us.
Whatever you do, don't deal with it alone. Keep being honest and ask for a helping hand when you need it. I love y'all, take care of yourselves and each other.
I just wanted to say that If you have suicidal thoughts or mental trauma or even if you don’t or just going through a thought time or neither just know that I love you and your loved by many and people and if you think that might not be loved by your family or people you know or just anyone just know they might even love you even more than your think. You have a purpose you are beautiful, kind, just be yourself and go after what you want to do. You are amazing, you got this, and things will get better in your life, you will do great things, and so many people and I are proud of you. Your future is bigger than your past and your past does not define you are awesome and a warrior. Don’t hate yourself simply because of your past, forgive yourself, love yourself no matter what because you deserve the world and the great things in it. I love you Have a wonderful beautiful nice day. Also how are you and your family doing today? Hope you feel better and your family.❤️ Be yourself no matter what you are, have, or what to be you are still amazing and you kind and beautiful always you are the light of the world. Stay safe. 💪🏽❤️. Have a beautiful day.💯❤️❤️💪🏽
Doctors just tell us what to go to God about!!! You must not give in to illness. Your boys and Glory need you. You need you! And you deserve the joys of life. You have to make up your mind that you’re gonna seek Joy and live happy and do and see as much as you can. Even on your sickest and worst physically challenging days you have to keep your hope, continue to seek Joy and hold on to your faith.
Believe God and pray for him to allow you to know him personally as HEALER. I ask God to return your faithfulness with more and more grace.
My thoughts and prayers are with you guys! ❤ I hope you overcome all obstacles and continue to grow and conquer, you two always make my day better ❤
Bro!! As a believer I am standing in prayer with you! My wife and I have love popping in and seeing your families journey over the years!! Brother rest in the fact that God holds your future and your family is in his hands! S&R4L!
You haven’t been “you” for a while, so while I am sad/shocked at the news, it’s nice to know what’s been wrong. This makes sense now. If you want to make a video, but don’t feel that you have anything to contribute, please know we are happy to see you both just as you are. Just have as much fun as you can, and we’ll like and comment. Sending prayers your way! Don’t try to make sense of it all. Just give God the glory through it all. Prayers 🙏🏻🙏🏻 Thank you for the update 🙏🏻🙏🏻
Wow, Cousin, my heart dropped when I read the caption of your video. And then I watched. Glad you went to the doctors and got checked out and a second opinion for confirmation. Thank you for sharing. This video may help someone. You, Glory, and those beautiful boys are uplifted in my prayers 🙏🏾🙏🏾 God is healer and way maker. Stay strong in your faith, take care of yourself, and remember God got this and you!!! Love to you and the family 🙏🏾💙🙏🏾
.May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips..💯
I’m an older subscriber and I absolutely adore you guys. I am praying for complete divine healing. Much love 💕
Matt, creating this video takes a lot of courage. To be this open and vulnerable about your recent diagnosis just shows how strong you are already. It’s also beautiful knowing how many people are in your corner who care and love you unconditionally. I will be praying for you and your new journey you are about to embark. I have watched you and Glory from the very beginning and will continue to support 😊
😊May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclipsToday I was confirmed negative for Multiple Sclerosis after having a horrible hard times, and feel the same way you described in your interview. Listening to you dr ubarlo share your overcome experience gave me the glim of hope I needed to hear. I am glad that there is people like you out there who just want to help other people who are struggling with the same issues. Your words gave me the courage I needed to hear today to know that it's ok. I can still be myself and now I'm enjoy my life the way I am supposed to. it is a blessing i came across you Dr.ubarlo❤❤❤
I hate that you’re going through this. I am so proud of you for going to the doctor and checking up on your health. Luckily, it is multiple sclerosis awareness month. My auntie passed away from it. You are one of my favorite RUclipsrs and I hate that you and your family are going through this. I am praying for y’all.
I'm praying for you and your family. God is a healer, raising faith in him. No matter what any doctor says, God has the final say! 🙏
My son was diagnosed with MS about 3 years ago. He is 34 now. He is doing well with the treatments and working out. It's different for everyone. He had issues with his eyesight and falling from leg weakness. Sending prayers and positive thoughts.
I can't imagine the courage it took to share this information with us. Thank you for your honesty and openness with such a personal matter. Medical diagnoses that change our lives are difficult to process and ultimately accept. You are blessed to have a supportive family to go through this with you and a doting fan base that only wants what's best for you. I pray that you find the path that is right for you and that whatever treatment you choose leads to long-term remission.
I was diagnosed with so many connective tissues diseases. I cried so much because I have a child with severe special needs. All I can think about is him… that keeps me in a dark place but I’m so grateful for my husband and our village. I just pray for him and not me. 😢 that god will guide him and that I will be ok.
Im sorry to hear that Matt, please take it easy, don't record if you don't feel like it, your health is important.
To say that this video hit a soft spot for me would be an understatement. 🥺
I was diagnosed with an Autoimmune Disease called Mixed Connective Tissue Disease (MCTD) about a year and half ago. It is a part of the Lupus family which is also seen as an ‘incurable’ disease.
For someone who has also been with their lifelong partner since I was 12 (now turning 30 this year), it broke me knowing that this could effect my future with my husband…something we have dreamed about building together since the day we met. It was also really hard coming to terms that something was ‘wrong’ with me with now the whole world seeing me as this fragile being (as if I am made of glass). My immediate family members also didn’t believe my test results or what the doctors were saying because they would state, “well, no one else in our family has this - how could she?!”
I went from living a ‘normal’ life by going to the doctor thinking I had a minor kidney infection (not taking any sort of daily medications at that) to being told I have fluid surrounding the lining if both of my lungs, the lining of my heart and my kidneys were leaking protein. I was then admitted into the ER and being wheeled every which way for MRIs, ECHOs, X-Rays while being prescribed 7 different medications (some through IV; some oral) and having my blood drawn multiple times a day as if I was the main source for blood in the whole hospital…
It was the most surreal moment of my life…I went through a really depressive time this past year by having to adjust to my new norm of carrying a pill organizer for my morning and night pills and having to see so many specialists every 3 months with bloodwork (some I didn’t even know existed)…if it wasn’t for the blessing of my husband though who vowed to be by my side through sickness AND in health, I wouldn’t of made it this far.
I am happy to say that my mind set has changed as I have been in a remission state for almost 6 months now. I have cut my medications from 7 a day to 2 a day for my ‘maintenance medications’ and I feel as though I am getting back to feeling healthy once more (I also switched to a Mediterranean/Vegetarian Diet and have made some adjustments to fit my needs better). PRAISE GOD!
I’m typing all of this to say that you are not alone in this autoimmune world and I am so happy that you felt comfortable enough to share this with us. If you or anyone else has read this this far, PLEASE DON’T BE AFRAID TO GET CHECKED OUT BY A DOCTOR! ❤ You truly never know how many people could be walking around with undiagnosed things that are just waiting to be discovered AND cured.
God would never put you into a life situation that he knows you could not overcome. Do not let this Diagnosis define you.
Bless you, Glory, and your beautiful family.🙏🏽✨
My mom LOVED you guys ! I started watching y’all because of her. She was diagnosed in 2012 when I was 11, and she fought it with everything in her until she passed in 2022. I’m praying for your health and sending love your way. Keep fighting 🧡!
I'm sending you much love❤ my mum has MS and was diagnosed when I was 2 I'm now 24. She's been amazing and I know you will be for your children and wife aswell! Much love 💕
Wow! That’s so crazy my mom was diagnosed when I was 4 & I just turned 25
I was diagnosed with MS in 2017, I was 16 at the time and my life got flipped upside down. It's a lot to take in all at once. But God is my healer and I've been calling on him more and I'm doing fine! I hope your journey is steady. I'll be praying for you🙏🏼 been watching you for years 💞
My husband was diagnosed about 5 years ago. With changing his diet( gluten free dairy free no processed sugars etc) it helped him a lot. He actually went to doctor for eye issues too and after long time they found it to be MS and it can be a struggle. Praying for God to help you. It’s a daily battle but God will be with you through it. Take one day at a time and be patient with yourself and it will be better after time. My husband tried the IV at first but changed to diet and it seemed to help him better than the medicine they gave him. However if it works for you please go for it whatever helps. I don’t want to discourage you from medicine but my husband found that diet and exercise helped him more.
I have an autoimmune disease that is sometimes debilitating and really hard to handle. It’s so important for you to go through the grief of the life you thought you’d have and embrace the life you have now. Thank you for sharing. I hope that treatment works well for you and that you can be in remission for as long as possible!! Sending love y’all’s way.
Which one you have?
The way I sat here and cried like we're related. Even so, that is a testament to how much I care about you all and I'm so sorry to hear about your diagnosis. I appreciate your bravery and vulnerability to share your story. Even while dealing with MS and the grief, you chose to share in hopes of helping someone else; such a beautiful heart. Love ya'll 💕
May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips
I'm dealing with Ms for 6 years. It's hard. No one to talk to. People don't understand me. Hard for me. I know you can do it. Stay up, and take your time. Sending love❤
❤May God keep using you to heal more people just as you treat my multiple sclerosis disease with your herbs medicine, great work Dr.ubarlo on RUclips.
Wow....wasn't expecting that video... but here we are...Matt, I pray for healing from the inside out! You're gonna get through this! Anytime I need a good laugh, you and Glory are in my rotation of vids I watch. A lot of times, I'll watch multiple videos on the channel at a time! Y'all never fail to make me laugh! Matt, you got this because I know God's got you! Understand that He wouldn't put more on us that we can bear. And I'm waiting for the testimony that's coming from this! And there will be one! Mad love Matt and Glory! From a fellow Baltimore native! Hope to meet y'all one day!
I was diagnosed with RRMS in 2017. It's been a journey. I've been in remission for some time now. Focusing on eating healthy and being as active as I can. Prayers for you. 🙏🏾🙏🏾