I was diagnosed with Multiple Sclerosis
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- Опубліковано 7 лют 2025
- Thank you guys for the prayers and stopping in to check on us ❤️
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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.
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
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 UA-camMay 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 UA-cam
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
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?
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
🙏🏿
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 ❤
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 UA-cam❤
”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❤
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 UA-cam
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.
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.
🎉 personally I think you're smart to stay out of medical mill. They just put you on poisonous meds that usually make you worse in the long run. If you're doing okay on your own personally I would just continue. Body is designed to heal itself if given all the right components.
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 ❤
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 UA-cam❤
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.
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.
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!
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 UA-cam❤
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 UA-cam
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 🤗.
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 UA-cam...
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 UA-cam
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 UA-cam
Thank you for your profession!!
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!
Hi. I have been living with MS for 20+ yrs. Pressing Forward and taking one day at the time.
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 UA-cam.
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 UA-cam
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.
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 UA-cam
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 UA-cam😊
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!
I'm praying for you, Slice. I'm so sorry to hear about this. God bless you.
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!!!
Just saw this Feb 7, 2025. Hang in there! Prayers and ❤️ love!
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..
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 UA-cam❤❤❤.
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.
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😊😊
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
This is my first time watching your channel. I know you may not even see this post since this was awhile ago. But I wanted to share with you my pastor was diagnosed with MS (not sure the type he has) at age 27, he is 78 now. He looks great, and walks amazingly well. Only recently he's been limping on occasion and I think it's when he goes off his strict diet. I think a strict diet and exercise with a lot of faith and prayer and daily bible study so you get closer to God will really help throughout you long life. It's also such a blessing to have an amazing strong loving wife, the support of family and friends and try your best to allow any stress roll off you. God Bless you.
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 UA-cam❤❤
Stopped in the middle of the video just to pray for you and your family Matt. GOD IS A HEALER ❤.
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 still in control. I'll be keepig you in my prayers.
Amen ! 🙏🏽
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 been diagnosed since 2001 I’m keeping you in my prayers
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'm so glad you have Glory.
God please hear their prayers.
thank you for sharing
it was important to share this with my boyfriend who is also Black who doesn’t know how to handle this yet. We found out today
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.
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.
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 🙏🏾❤️
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.
Thanks for this. I was just diagnosed during a 7 day hospital stay for numbness on my legs on 1/19/2024. I could use some support. Especially not knowing anything about the condition. I've been doing research like crazy. I AM SCARED! But I want to win! The fatigue is horrible I feel so so tired but I be just telling myself 'just fight it'! I just had my appointment on 4/3 with neuro. I do have another appointment with another neuro in May because I felt the same just need another confirmation to start treatment.
Making a doctors appointment now. Thank you for being vulnerable and honest about this.
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.
I have RRMS, diagnosed a couple of years ago. I think the best thing I did for my MS was to get on a high efficacy treatment immediately. I laughed when you were talking about this being a older white woman's disease, since that's me now. We got this, sending you love and support!
I am sorry to hear that Slice. I will keep you and the family in my prayers. 🙏🏽
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.
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.
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 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.
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.
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
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 🙏🏽 ❤
You nailed it. I was recently (recently for me) diagnosed with MS, 2021. I had an attack. Woke up dizzy and throwing up, and it didn't stop for months, it still hasn't.. I still am very imbalanced, and the sedentary lifestyle after the attack has kicked my butt. I have good days and bad days. Some days I feel like I got this, most days I am defeated. I am letting it get to me, and I don't know how to not allow it to do so. Wishing you the best and sending very positive thoughts your way. You seem to be taking it with grace. Just remember (I don't say this enough to myself...) You have MS, MS doesnt have you.
Hey brother,
Stay strong. God's got big plans for you man.
Thank you for sharing this video.
I'll be praying for you and Glory
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 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.
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 didn't think a video on UA-cam 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.
Thank you for sharing about your experience with MS. Your transparency will help so many people. 🙏🏽
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.🙏🏽✨
I think the roughest part about your first year with a chronic illness is mourning your old life and having to let go of this societal programming of how we are "supposed" to handle our day to day life and not being able to live up to that a lot of times as a "spoonie" (spoon theory reference). You are not alone, find your community that you can vent to that get it; it is very helpful to vent to people that KNOW what it feels like to have a day like yours. I know it is scary but a lot of people with MS live pretty able but know that the grief and all is expected and normal. You do feel like your healthy self died but you are strong enough and you've got this.
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. 💝💝💝💝💝💝
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“ ✊🏾💯🔥
Sorry for your MS diagnosis. My neice has MS and I know it can bring many challenges. She graduated from medical school and went years before antoher major rehlapse. I pray that therapy is successful in slowing down MS progression for you. I also pray that you keep that beautiful smile, your sense of humor and purpose. You got this!
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.
❤God continue to bless your family
My sister has rrms, she’s 42, we’re black British of Caribbean descent, it came as a shock when she was diagnosed about 8 years ago. I do have prior knowledge of MS, thanks for sharing your story, very educational and informative video, I wish you all the best in health and happiness x
.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 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.
Praying 🙏🏾 Coming against any negative and non-live giving words spoken over you in the name of Jesus.
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 UA-camrs and I hate that you and your family are going through this. I am praying for y’all.
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. 🙏🏾🙏🏾
Seeding you some prayers Matt.
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?
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 💞
I have MS and it took me a long time to figure out what to do about it but I just want to tell you to never give up fighting because I said I have MS but MS don’t have me so we have to keep fighting for the cure and hopefully it will come soon. GOD BLESS YOU AND THIS IS ONLY THE BEGINNING 🙏🏾🙏🏾🙏🏾😇😇😇👍🏾
My husband and I prayed for y’all tonight. God is a healer. Keep clinging to him. God’s got you! 💜💜
That's how I felt every time I got a new diagnosis. Pure denial, but after the 10th illness it no longer was denial but anger as to why I had to go through all this because I'm now over 18 different illnesses. But then it subsides and you find the fighter in you. I wish you the strength to fight and keep living as best you can with joy and peace. With the support. I have at best 20yrs left to live and that's if my heart holds out that long. You've got this and you're stronger than you give yourself credit for.
You will 😊😊😊😊
@@thebignastyone1984 that's my hope too. But it's in God's hands. I learned to let his will be done. I just always hope that people will keep fighting no matter how hard it gets. You've got a reason to fight and that's you. Whether it's for your own mental sake or for your life. Up to us to live and walk the path set before us. Can be miserable or you can choose joy and peace through the trials and tribulations. An maybe you'll be the encouragement somebody else needs to face there battle. Thank you for your kind words. Peace be upon you
@nirving26 you're welcome. You've made it this far and you will go further. You've fought this long.
Been living with it for the past 7 years, and boy is it worth having a village through it. I had headaches since I was 15, and then at 23 had my first relapse where I was also diagnosed. I joined the Ocrevus trial and it helped so much! They say MS affects men different then women, and personally, I dont know too many men, but know a lot of women with it. It would be helpful for you to document your journey as my son will have a 20% chance of having it as well in his life. Prayers to you and your family always.
..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 UA-cam
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.
Hi Matt, first and foremost I want to say my heart goes out to you and your family. My husband was diagnosed with MS in 2010. During this time (2010) his MS episode was very intense, we found a diet plan called Gods Diet. This diet made such an amazing impact on his health, mind and spirit. I know you are strong and have a strong supportive family behind you but I do recommend finding an MS support group. By doing so you will find others that will be able to relate to you and give you advice and/or guidance on how to deal with this. Please continue to smile and know that you are an amazing father and husband and that will not change just because of your diagnosis. Continue to pray and keep your faith strong. MS is not the end of your journey it’s the beginning of a new chapter in your journey.
I was diagnosed in November with MS. I often feel bad for people struggling with diseases or any health issues in their life and they dont have anyone to help them or be by their side. Just like you im so grateful for my spouse. He has been the main reason i dont break down everyday. Taking this journey one day at a time. #MSWarrior
RRMS GANG! Got diagnosed in 2013. I had my boss read the results before the neurologist could tell me. And i saw the fear in his face before he told me. And the 1st thing he said was... call the neurologist and tell her I SAID YOU NEED TO BE SEEN BY TOMORROW!!! Then he told me the diagnosis. I still haven't really come to terms with it. Every day is different! Prayers to you! Join a support group!
It’s a journey
youre so fucking strong dude. been watching u n glory for years now. U FINNA PUSH THROUGH THIS N JUST GO UP