My MS Story| Symptoms| Diagnosis| Treatment| Feelings
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- Опубликовано: 7 сен 2024
- Hi! My name is Sierra. I was diagnosed with Relapsing-Remitting Multiple Sclerosis (RRMS) in April 2016. My MS Journey has allowed me to learn about the disease and how MS affects my body. I will discuss my initial symptoms of MS and how it affected my feelings and thoughts. I'm sharing my MS story to inspire, uplift, motivate, and advocate for people living with MS.
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Thank you for sharing your testimony. I was diagnosed in February 2021 at the age of 61, after 25➕ years of symptoms with no diagnosis. God carried me all those years and I know HE will continue to carry me! You continue to stay strong and to stay focused on God! I look forward to hearing about your progress!
Thank you so much for your support and blessings!! Yes ma’am, God will continue to carry you. 🙂 I could not imagine going through my MS journey without God. He is my Rock! 🙌🏾
I'm 62 and I have a feeling that I have MS. I'll be going to the doctor "again" and insisting on tests. I think they don't even think about MS for older people, but it can happen.
@@sierrachairston dope content. Thank you for sharing your story
Hi! Advocating for your health concerns and needs is essential in getting your answers and hopefully feeling better. I hope your healthcare team will listen and be supportive as you discover what is going on with your body. What symptoms are you experiencing? Yes, MS diagnosis can happen at any age. I am sending you well wishes and a hug! 🙂❤️
Thank you so much for watching my videos and your support! 🙂❤️
Thank you. Diagnosed in 2010 at 44 years old. I have never met anyone else with MS so it's been REALLY TOUGH but you strap up your boots and modify your life so you can survive. Without my faith I probably wouldn't be here today.
Hi! Thank you for reaching out and sharing! How are you doing? How is your MS? Do you need any MS resources? I agree! Strap up your boots and modify your life so you can survive! 🧡Faith carried me in toughest moments. I’m thankful for the Holy Spirit and the Word of God for guiding my path.
@@sierrachairston yes and Amen. I have RRMS. Been dealing with severe spinal pain daily for 3.5 yeaes. I have had 76 falls last year and as a result the VA is supplying a power wheelchair so I can attempt to reclaim some of my life again. I would appreciate any helpful info that you have learned and or resources that have helped you. I know I'm older but it hits harder when you alone have this desease
Disease and no one has this challenge but you. I just want to survive this and thrive thoiugh it. 🙏🏽🙏🏽🙏🏽
Thank you for sharing! I understand. You can, You will!! We are fighters! We are Warriors! 😌❤️❤️
Hi! 🙂 I understand. I'm glad you will receive a power wheelchair and are working towards reclaiming your life again. MS can take so much out of you, so having self-determination to reclaim your life is outstanding. What I found helpful in my situation was engaging in the MS Community, prayer, incorporating self-care and energy conservation, learning about MS and ways to manage my health and care. I hope these resources below ⬇️ are helpful. 🧡
This is a helpful article from MS Focus Magazine (Multiple Sclerosis Foundation)
msfocusmagazine.org/Magazine/Magazine-Items/Posted/Alone-with-MS-The-Symptom-People-Don-t-Talk-About
Below are some helpful resources from the National Multiple Sclerosis Society that specifically talk about reclaiming your life. You will find articles from the Momentum Magazine and other helpful resources.
www.nationalmssociety.org/Living-Well-With-MS/Mobility-and-Accessibility
***Some of the Articles**
momentummagazineonline.com/roll-with-it/
momentummagazineonline.com/on-the-move/
momentummagazineonline.com/awesome-aliases/
Living Well with MS Resources from the National Multiple Sclerosis Society
www.nationalmssociety.org/Living-Well-With-MS
Resources and Support from the National Multiple Sclerosis Society
www.nationalmssociety.org/Resources-Support
MS Society's Library & Education programs website link, which consists of the online Program Series, brochures, educational videos, momentum magazines, webcasts, and more.
Below are the Library and education resources ⬇️
www.nationalmssociety.org/Resources-Support/Library-Education-Programs
Thank you for sharing your testimony. I was diagnosed in 2018 after decades of headaches ( bad migraines). I research what my symptoms could be and I went to the neurologist and told him that it was either MS or Lupus, he dismissed what I was telling him, I kept having these symptoms and when I went back he decided to do the test for MS and it came back positive, once I was diagnosed. I changed doctors. Now 2022 I’m having spasms and numbness and more but I know that God is a healer of all.
Hi! 🧡 You're welcome! I'm so glad to hear that you advocated for your health despite your challenges. I'm glad you got the answers that you needed. You are so right; regardless of our symptoms, God is a healer! 🙌🏾😇
Thank you!! I am 48 and have felt so alone and embarrassed about how bad I feel and look when walking and talking. Just got diagnosed with MS last month, they think I have had it 20-25 years. You have given me hope!❤❤❤❤❤
Hi Lynn!! Thank you for sharing your story! I’m sending you a hug and positivity!🤗❤️❤️ I understand. For years, I hid my symptoms because I was embarrassed of being judged and I was too invested on what others thought about you. Although, you live with MS, you are not your MS. When you are ready show yourself to everyone, use it as an opportunity to educate others on what MS is and how it affects you. I’m sure someone is waiting to hear your story so they will feel uplifted and supported too! ❤️❤️❤️
I’m
Scared too I just found out I start infusions soon her story helped me and I’m praying for you Lynn
61 and dx last week
“How could someone like me get something like this?” Exactly! Thank you for sharing your story… and a book, congrats!
Hi! My pleasure! I’m glad you can relate to this statement. How are doing? How is your MS going? Thank you so much!! 😊
Thank you for sharing your story! This resonates deeply with me as a Black woman that was recently diagnosed with MS. Your spirit is so beautiful and you’re definitely inspiring people. ❤
My pleasure! I appreciate your comment and support!🧡😊 Thank you for sharing! How are you doing now?
@@sierrachairston I’m doing okay. I was diagnosed a few months ago and I start Ocrevus next week. I’m nervous but optimistic and I’ll be sharing my journey here too. 🫶🏾
Okay, I understand. Stay positive and optimistic, rest, and incorporate self-care in your health journey. I’m happy that you will be sharing your journey too! People living with MS need inspiration and encouragement throughout their health journey. 🧡
I have everything that you are talking about. This happened to me in 2016 I go to the doctor every 3 to 6 months they tells me something is wrong with you. I can’t believe it I fall down my leg shakes at night the numbness, the heart hurts the spasticity , the shaking can’t get an answer. They tell me I need to go see a therapist. I’m . so tired nobody can tell me or give me an answer but your story I got it all. Thank you for sharing it.
Hi! It's my pleasure! I understand. I was misdiagnosed for years, and my primary care doctor told me at the time that it was in my head. Unfortunately, by the time I arrived back at her office, I was walking with a limp, and she referred me to a neurologist. Months later, I was diagnosed with Multiple Sclerosis. After that experience, I learned the importance of advocating for my health. Getting a second opinion is okay if you believe it will benefit your health. Always advocate for your health and keep a record (video and written). I hope you will get the support you need and a second opinion. It's not in your head.
I just got diagnosed last week. RRMS. I just turned 41. Started feeling bad last Spring, nothing before that. Thanks for sharing your story. 😢❤
Hi! My pleasure! Thank you for sharing! I understand. I have RRMS, too. A year before receiving my diagnosis, I started to feel bad; my symptoms worsened; I began to fall and experienced vertigo, headaches, weakness, and numbness. I know this is a difficult time for you, but know that you are not alone, and support is available. How are you doing now? How is your MS going?
P.S. I’m sending you positivity and a virtual hug! 🤗🧡
@@sierrachairston So far I’ve just had the 5 rounds of steroid infusions. Spent 4 days in the hospital. Feeing overall horrible right now and I’m really scared and angry. I’ve got some deep rattling coming from my diaphragm that I don’t understand when I breathe, tingling in my diaphragm, arms and legs, and not really balanced when I walk with heavy legs. I think they caught it early but I don’t know.
@@Gigiroo Okay, I understand. It seems like your health care team is trying to help stabilize your MS symptoms with different forms of treatment. I can’t imagine what you are going through. I know it is breaking your heart, and you are really scared and angry. How you are feeling is normal. I want to encourage you that you are still valuable and needed, and it’s alright to be upset, but keep fighting because you will overcome this life challenge. This is a big life adjustment; sometimes, it takes time to understand. It may seem impossible now but try to rest and relax your mind and body because stress and worrying can further impact your MS symptoms. Try to journal to get your thoughts out, listen to some relaxing music, play your favorite music or podcast, or watch something that will relax you or make you laugh. 🧡
When you are ready, I can send you some helpful MS resources. My email is info@sierrachairston.com.
I haven't finished your video yet but I don't want to forget - I'm so glad that your professors were so understanding and accommodated you! And also thank you for being a social worker!🥰 We need more amazing people like you.😘 💐 Back to the video.🤓❤️
This comment made my day!! ❤️ I appreciate your support and kind words. Thank God for sending excellent professors my way. I love being a social worker and using my transferable skills to live out my purpose. Sending you hugs 🤗😘
Thanks for sharing!
I'm a MS Warrior as well. Keep Pressing Forward 🙌🏾🙏🏾
Thank you for your support! 😊 I wish you many blessings in your MS Journey! 🧡🙌🏾
I'm a Millennial with MS as well. I was diagnosed in 2013 in my early 20s. Thank you for sharing your story. It really helps to hear from others affected by this chronic illnesses
Hi!! 🙂🧡 Thank you for watching and your support! I’m glad this video was helpful! It is my hope to
uplift and encourage others affected by chronic illness. How are you doing? How is your MS doing?
@@sierrachairston I'm hanging in there. Not doing the best as i usually have my relapse in the summer months because of extreme heat but I'm good. Trying to diet and exercise to help. Thank you for asking. How are you doing this season?
I definitely understand!!🧡 I’m so glad you are hanging in there. Take one day at a time. You have a good plan! You’re welcome! The summer months are tough for me too. If I spent too much time outside in the sun and don’t get enough shade, cool air, and hydration, I feel horrible. I feel completely exhausted. Some things that help me in the summer season is relaxing and resting, using cooling towels, staying hydrated, staying cool as much as possible, and diet & exercise. I had an MS relapse one summer and it was no fun, I experienced the worst discomfort and pain in my life. Sending positivity and a hug 🙂!
Great testimony! I'm experiencing symptoms now. Going to doctor soon. You are a inspiration. God 🙌
Thank you Carla! I hope your doctor’s appointment goes well and you find out what is causing your symptoms. I’m sending you positivity and a hug! 😊❤️God is so good and faithful!! 🙌🏾
Thank you for sharing your story. 😊 I was diagnosed with MS in November of 2023 I'm 46 years old. I really didn't understand the 😊 progression of how this disease works. All I did was Google it and read the definition. One night while at work I decided to get on RUclips and see what someone had to say. The only sounds and symptoms I'm having is double vision when I read small handwriting on my phone or on paper and every now and then I will get spasms in my arm or it would last I would say 1 to 2 days at a time. The pain feels like a needle just poking me and then a couple of days later the pain which is go away. I started wondering what was that all about. As a matter of fact I'm going to mention these episodes to my primary physician. Looking forward to more videos. I came across your channel. I did like and subscribe thank you.😊
@@precious2511 Hi Precious! Thank you for sharing! I understand. MS symptoms and progression are different for everyone. I Googled information about MS, too, lol! Different MS organizations offer a lot of information and resources: the National Multiple Sclerosis Society, the Multiple Sclerosis Foundation, and the Multiple Sclerosis Association of America, to name a few. I've experienced spasms in my arms and sharp needle pain that comes and goes. You should mention the episodes to your neurologist; it helps them manage your MS symptoms. Thank you for your support and for watching my videos! I appreciate you subscribing to my RUclips Channel, too!
*Some MS Resources
www.nationalmssociety.org
msfocus.org/Home.aspx
mymsaa.org
Information and Resources for People Affected by MS
(Click on View Flyer link to Download PDF- National MS Society)
www.nationalmssociety.org/for-professionals/for-healthcare-professionals/patient-resources
Carepartner Support Resources for People Affected by MS
(PDF Handout- National MS Society)
nms2cdn.azureedge.net/cmssite/nationalmssociety/media/msnationalfiles/documents/calls-carepartner-support-resource-list.pdf
National MS Society Education Programs and Library
www.nationalmssociety.org/resources/get-support/education-programs-and-library
@@precious2511 😊🧡
Fellow MS Warrior here since 2005
Hi Fellow MS Warrior!! That is amazing!! 🙂🧡 Sending you positivity and a hug! How are you doing? How is your MS?
MAY GOD CONTINUE TO BLESS AND KEEP YOU IS MY PRAYER!!!! MANY BLESSINGS TO YOU 🙏🏽 🙏🏽🙏🏽 AND MUCH ❤❤❤❤ TO YOU AND YOUR FAMILY
Thank you so much for your prayers and well wishes!! ❤️❤️❤️😊
Thank you for sharing! I have a similar story of my doctor dismissing my symptoms. I wasn’t surprised when I found out because I too had looked it up. lol Thank you again for sharing!
You are such a wonderful inspiration. I am awaiting my first mri in about a month. I have been falling dizzy tunnel vision shaky hands and twitching in my legs. I'm scared but I know God has a plan for me. I'm so thankful for your page.
Hi Kelly! Thank you for watching and your support! I understand how you may feel. I hope your mri goes well. No matter what challenge or difficulty you face in any season, God will always have a plan for you. 🙂❤️
I just want to say thank you I have to share this with my husband is 2023 and you to the doctor. Never heard the story but I got everything you talking about.
My pleasure!
Thanks for sharing your story. I am going through a period now where I am struggling to swallow. It's unpleasant, but I had the same issues about 15 years ago and it eventually went away, so I am hopeful that within a month or two it will not be so bad. Just got to be patient. I wish you all the best and hope your future is bright 😎
Hi Atana! I’m sending you well wishes, positivity, and a virtual hug. I hope that your swallowing challenges will resolve soon. You are right; being patient is the key. Thank you so much for your kind words and support! Hoping that you have a bright future too! 🙂🧡
Thanks for your VDO. I was diagnosed MS in January 2021 when my half right from head to toe lose of sensation; temperature and pain. I'm now finding more information about diets and everything that would slow down the relapsing.
Hi Chaweewan! 🙂 Wow, I could not imagine how you felt when the side of your right head to your toe lost sensation and other symptoms you experienced. I know you were very concerned. It sounds like you have a plan in place. Educating yourself about Multiple Sclerosis, MS diets, and more will be helpful, and working with your neurologist and healthcare team to support you along the way. Are you currently on any treatment for your MS? How have your MS symptoms been?
@@sierrachairston Hi Sierra! My condition right now is getting better my right part of my body can feel temperature and pain ~90% compare to the left side. The doctor considered to stop prescribe a steroid for me since last month but I still need to have an immunosuppressant everyday. I think I will take notes when notice anything abnormal in a daily life before seeing doctor in 3 months ahead. Hope your condition stay calm as well.
Hi Chaweewan! Okay, great! I'm glad you are feeling better. It sounds like you have a good plan in place! I wish you all the best in your MS journey. I hope your doctor’s appointment goes well. I'm doing good. I do have my good and bad days though. My MS treatment is going well. I've been staying active. I have my follow-up appointment with my neurologist next month. Thank you so much! 🙂🧡
Hello there! I don’t have ms but your story encouraged me. I have been struggling with digestive problems erosive gastritis and colitis unspecified to be specific. And I have really struggled for years but sometimes we just have to be grateful because no matter where you are you are better than someone out there. Thanks for your encouraging message
Hi Mary!! 🙂❤️Thank you for your support! I'm so happy that my story encouraged you! How are you doing now? I agree with you! I had to learn to be grateful and give thanks despite my health challenges. When I have a terrible day, I always see something that reminds me that I'm doing better than someone out there, and I get back focused on what is important.
@@sierrachairston Amén to that! By His grace I am blessed to be doing way better than where I was. Thanks fully charging my diet has really really helped me and though I still have struggles at times when I eat certain foods but at least I have been able to know what I should eat and what I should stay away from. I adopted a vegan lifestyle and it’s paying off. Thanks once more my friend , I am glad we both are serving the Lord through our circumstances. Stay strong and God bless you ❤️🙏🤗🤛💪
I was diagnosed 2 years ago on my 34th birthday I lost function in my legs I had to learn to walk again my hands and feet would always tingle I had restless legs at night it got so bad I could only sleep sitting up and on the balcony in the cold for my legs to be calm my legs felt heavy even a blanket on them would feel like a ton of bricks it’s a little better now but not so much because of how I adjusted to walk I messed up my hips and now have necrosis in my hip and need surgery so I’m back on bed rest until I can get it pray for me
Hello Ciara I came across your page and I listened to your testimony of finding out you had MS it was a lot like mines. It's always good to hear someone else that is battling the same disease that your battling like some things you might go through that I have not went through so when I do end up going through I'll know it might be my Ms and I can deal with it accordingly I've been having Ms now for 18 years now I'm 41 by Gods Grace. I have my moments and my days where they're either hit or miss but I do wish you the best in going through your battle with this Ms I will continue to follow you and I am a new subscriber thank you for sharing your journey.
Hi! Thank you for listening to my testimony. I really appreciate your support! 😊I have my moments and days of hit or miss too, MS symptoms are unpredictable. I feel encouraged and motivated to keep going hearing from you. MS is a battle and we are truly MS Warriors. God is good! Thank you for subscribing and following me on my MS journey. I look forward to sharing more about my Multiple Sclerosis. 🧡
Your story sounds so so similar to the last few years of my life… wow. Even the dr dismissing me. Thanks for sharing.
Hi! 🙂You're welcome! Wow, thank you for sharing! It was challenging visiting the doctor several times and not receiving a solution, but I stayed persistent and kept going. How is your MS now?
Thank you for sharing your story. I am experiencing muscle weakness particularly in my lower extremities and at times have experienced waking up to a numb foot and leg. I’ve followed up with my pcp and neurologist but still have no diagnosis. It’s been over a year now and still no answers. Although I’m frustrated with ongoing fatigue and muscle weakness coupled with joint and muscle pain at rest, I’m encouraged by your video.
Hi Sonya! I am sorry you are experiencing those symptoms. I am sure you are very concerned and want some answers. I want to encourage you to continue advocating for your symptoms to receive tests, imaging, etc., needed to get your symptoms addressed, even if it means getting a second opinion. I hope you can find out what is causing your symptoms and start to feel better soon! I'm sending you positivity and a virtual hug! 🙂
This is the first testimonial I have seen that I can relate with the symptoms and you and you didn't sugar coat or dismiss your struggle with MS. It is a disturbance on daily life and people don't understand MS and can sometimes have many incorrect preconceived ideas. Lay it on him and he guides us.
Thank you for sharing, it will definitely help.
Hi Jessica! I’m so glad my video helped. I spoke from my heart. MS can definitely cause a disturbance in daily life and can be misunderstood. MS is one of kind and definitely needs to be acknowledged and discussed.🙂🧡 Sending you well wishes and a hug!
You are a light. Thank you for sharing your story. ✨🙏🏻
Thank you so much! I truly appreciate your support! ❤️😊
Thank you for sharing your story! I found it helpful to hear what your early symptoms were like. They sound familiar unfortunately
Hi! My pleasure! I'm glad you found my video helpful! :) Have you been diagnosed with MS?
Thank you for sharing and keeping it real.
Hey Jeff!! I’m glad this video was helpful. I had to keep it real Jeff, lol! Transparency equals growth. 🙂
Thanks for the video. Getting my MRI on brain and spine tomorrow morning ❤
Thank you for watching my video. I hope your MRI went good. Wishing you all the best! 😊❤️
I have had that too they said it was normal but when I read the report it showed the narrowing of my spine and scoliosis and the old bruise on my brain from birth. I have cerebral palsy and was recently diagnosed with polyneuropathy
Hi Kelvianna! Thank you for sharing! How are you doing now since your polyneuropathy diagnosis? How is your cerebral palsy doing?
@@sierrachairston my cp has been overshadowed by this nerve damage
Okay, I'm sorry to hear that. What symptoms do you experience from the nerve damage?
Thank you for sharing your testimony, you are so open and honest, in addition to being a Christian, you touched me deeply.
I'm old enough to be your grandma, but she isn't a barrier with connecting.
I'm happy for you about going through grad school,
God bless you sister,
Love and prayers ✝️❤️
Hi! Thank you so much for your kind words and support! It is my privilege to represent the perspective of a Christian and woman of God. I’m touched that my story reached you! God is good! I'm sending you positivity and a virtual hug! 😊 🧡
Thank you for sharing your story❣ Best whishes to you in your MS Journey. God is absolutely amazing 🙏🙌❣
Thank you for your support!!🙂 I wish you all the best in your MS journey! 🧡God is amazing!! 🙌🏾😇
Your story is so encouraging. I was diagnosed in May and it has been scary but ive been in my word. God heals I’m very happy to hear you are feeling better
Hi Kristen! 🙂🧡 Thank you so much!! I understand. Being diagnosed with MS can be scary. Prayer and reading God’s Word continues to keep me grounded and strong! How are you doing? How is your MS doing?
What a wonderful testimony of faith . Faith is the victory that overcometh the world !
Hi! Thank you for your kind words and encouragement! Faith is essential to a believer's ability to have supernatural breakthroughs and deal with life tests. 🙏🏾 We must put our faith and trust in God, no matter what. Thank you! 😊
Thank you for sharing your story. I suspect i have MS. In 2005 i was Diagnosed with Fibromyalgia but i think it was a wrong diagnosis. You are beautiful and much appreciated. 😊
Hi Leslie! You’re welcome! How is your Fibromyalgia doing? I encourage you to advocate for yourself so you can get the exams, test, labs and imaging needed to address your symptoms and concerns. Nobody knows your body like you do. I hope all goes well for you! I’m sending you positivity and a hug! 🙂❤️
Thank you so much for sharing your experience. This helps people.
My pleasure! I’m glad this video is helpful! 🙂
Thank you for sharing your story. I have a lumbar puncture scheduled next month and my second MRI this time with contrast this month...while in nursing school 🤦🏾♀️. I'm hopeful with managing it with my diet though. Thanks again!
I wish you the very best with your lumbar puncture and second MRI. Be positive and be around people who will encourage you and uplift you in your nursing school and health journey. Advocate for yourself. Stay encouraged and keep going!❤️ Thank you for watching. 😊
It is so crazy that I have gone through all of your steps in life. Brain tumor acid reflex Gerd gallbladder removal numbness of arms heart palpitations and restless leg syndrome memory fog speech delay hip pain numbness of fingers trigger finger and more. To this day the doctor says nothing is wrong with me. 2012 to today I have been fighting myself. Thank you for sharing
Hi! 🙂My pleasure! Thank you for sharing! You have went through a lot. Did you receive any treatment for your brain tumor? Have you received imaging or other test to rule or rule out MS? How are you doing now?
Thanks for sharing! I had my MRI yesterday and the DR office called to see me Monday. I have a lot of MS symptoms . Lets see what he says.
Hi Michelle! You’re welcome! I’m sorry about you experiencing MS symptoms; I know it isn’t easy. I hope everything goes well on Monday. Whatever happens on Monday, keep moving forward in your life and continue to advocate for your health. Surround yourself with people that are positive and will encourage you. Take one day at a time. I am sending you a virtual hug! 🙂❤️
So what happened? What’s the update?
I'm glad I came across your video. I have a feeling that I have MS. My father had it and I'm experiencing many symptoms. Thank you for sharing your experience.
Hi! Thank you for watching and your support! 🧡 MS symptoms present differently for everyone. It is truly an unpredictable illness. I understand your concern, especially with your father's history of MS. I hope you can schedule a doctor's appointment soon to address your symptoms. Sending you my support and a virtual hug! 🙂
Did you ever get diagnosed? I have symptoms but brain and full spine scan all clear. Hope you are well thanks.
A top neurologist here said no, but another said yes. I have a moderate amt of brain lesions. It was confirmed after a spinal tap showed oli. bands. Dr recommended Ocrevus.
@@raineynight I had brain, c spine, thoracic and lumbar MRI and there is no evidence of demyelination. I also went to the opticians and had an OCT scan which was clear and also my neuro exams all normal. Do you think I should take that as gospel? I hope you are doing well
@@raineynight what does AMT mean?
Thanks for sharing! Been having 10 years of crazy symptoms, I think I had a relapse during Bar Prep last month 😩 MRIs in 2 weeks for diagnosis
Hi Sosha! I hope all is well. I understand what you mean. I have had some crazy MS symptoms for the past few weeks. I'm waiting to hear back from my MRI. I want to encourage you to keep going, speak blessings and life over your situation, and continue to work towards passing your Bar exam. Rest and take time for yourself. 🧡
What symptoms were you having? What was the outcome?
Finally a realistic video..I started my symptoms 2 weeks ago..few days ago I had to call the ambulance cause my right side got numb hands got stuck in one position thinking stroke going to happen then my left side got numb mins later..I use to complain about pain to my fam everyday felt like I was going crazy..finally get my mri on the 14th..plus my dad have ms..just hope for me it's not the case
Hi Rayah! I could not imagine how concerned and afraid you must have been when the incident occurred. How are you doing now? How is your Dad doing? I'm sending you prayers and a hug! Take some time to relax and rest your body. I hope you will get the answers to your questions soon after your MRI. I try to keep my MS journey authentic to help people living with MS feel supported. I appreciate your support! 😊🧡
@@sierrachairston my doc called me yesterday and set me up a appt for a mri on the 14th..I been ignoring it thinking I'm going crazy..my dad is good he still have episodes of being paralyzed on one side blindness that happens sometimes etc he found out in 2000...when I hear other ppl story of MS that's worse than mines I question if its MS but ik ppl have different symptoms..so ya waiting on this appt on the 14th and I will let u know ❤
Okay, great! I understand what you mean. Our bodies have a way of telling us if it feels any discomfort or pain, lol. Wow, your Dad is an MS Warrior and fighter. I'm glad he is doing good overall. Tell your Dad I said hello, and I wish him all the best! I agree with you. People have different MS symptoms. Yes, please update me! Either way, on the outcome, I want to let you know to be encouraged and continue to advocate for your health, and everything will be okay. 😊🧡
@@sierrachairston I appreciate it❤❤❤❤
@@Ray-hv1hg did you get your results?
Glory to God, am happy for you, God is good
Thank you so much!! God is good! 😇🙌🏾❤️
I was diagnosed in 2002. I recognize the finger shaking. Did you have optic neuritis? That was my biggest issue, along with drop foot. I'm a welder so getting hot then experiencing drop foot was an everyday thing. Glad you're working through this.
Hi Nick! I did have optic neuritis. I could not imagine what you went through. How are you doing now? I’m doing better, I still have my good and bad days. Thank you so much for watching my videos and your support!🧡
Hi, I'm good now but that could always change
@@nickmalveaux6131 Okay, great! I understand. We have to take one day at a time because our MS symptoms are unpredictable. 🙂
Thank your for sharing
Thank you my Sister in Christ 💗
You’re welcome Christina!! 😊💗 I hope all is well.
It's a wild ride for sure. Hang in. You seem pretty resilient
You're right, Spencer; it's a wild ride! Unpredictable moments, lol! Thank you so much!
I am going through something similar I’ve been researching some of the stuff that I’m saying is what I’m going through I was rushed to the emergency room on April 30 and haven’t been at work since then they still trying to figure out what’s going on with me
Hi Rochelle! Thank you for watching my video. Wow, I can't imagine what you are going through and how you are feeling. I pray that you will have peace and find out what is going on with your body. Keep advocating for yourself and your medical needs. Surround yourself with positive people and find ways to reduce stress. Stay positive, and don't ever give up. 🙂❤️
Praise God that you are doing better. Thank you for sharing your testimony. This came at the perfect time for me. You are such a blessing. 🙏💕
Hi!! 🧡 Thank you so much for watching my video! God truly blessed me and I give Him all the glory! 😇 How are you doing?
@@sierrachairston Amen! I am well. Thank you for asking. So glad I found your channel. Continuing to pray for you. Take care.
@@EH-MiM Thank you so much!! 🙂🧡 Take care as well!
I enjoyed reading your Ms story I have MS and I was diagnosed in June 2022 your story is so inspirational to me
Hi Sonya! I’m so glad you enjoyed my MS story! I am honored. 😊 I’m sending you positivity and a virtual hug!! How are you doing? 🧡
@Sierra C. Hairston I am doing okay I have my good and bad days.
Okay, I understand. 🙂🧡
Ty very much for sharing ❤
You remind me of me, that's the samething I felt. This can not be my life, why me? I've never been the party type, no drinking, no drugs of any sort ever. Then boom💥 I hate it!! TFS your testimony 🙏🏽 it's definitely inspiring🧡🧡
Hi! Thank you for sharing! I’m glad you could relate to my story. I understand, lol. My pleasure! I hope you are doing well in your MS journey. I’m sending you positivity and a virtual hug! 🧡🤗
@@sierrachairston thank you! I'm trying everyday🧡🧡
@@j.y.8 I’m glad you are trying everyday 🙂 Keep going! Don’t give up!! 🧡🧡
Tank you for sharing your story
You’re welcome! Thank you for your support! 🙂
You’re just gorgeous! Love your energy. Wishing you all the best 💜
Hi! Thank you so much for your kind words and well wishes!! 😊❤️
Sending blessings you way! Thank you for your testimony.
I'm currently experiencing some symptoms of yours but the thing pissing me off the most is hand shaking. The neurologist I've been to said it's "not a common trait in MS and she doubts this is it", although I have also numbness in my legs and hands, painful spasm and general spasticity and ear tinnitus as well 🤷♀️🤦♀️. I hope to find answers sooner than later, cause I feel like this doctor didn't believe me 😕.
Hi! 🙂Thank you for your support! I’m sorry you are experiencing these symptoms. I can’t imagine your frustration, I know you need answers asap. I hope you are able to get all the exams you need to find out what is going on with your body. Did your neurologist schedule an MRI?
Thank you, I did learn a lot from your experience to help me with my own
Hi! I’m glad this video was helpful. You’re welcome! 🙂🧡
Great video I do hope you do recover from this Multiple Sclerosis sickness 😷 I to am dealing with my version of this sickness that took over my right side both my arm and leg are affected so my driving is no more I rather not drive at all so I gave up my License to the dmv I love to art but since I'm a right handed person and my right arm is affected I can't even write my name down on paper so I'm just doing what my doctor tells me to do I was told to take the medicine on the shots I have pills that I have to take and a leg brace for my right leg .also lost my job I worked as a Quality Control tech in a chicken plants before. Now I'm just waiting until this cure for Multiple Sclerosis gets her I'll keep waiting til it gets here
Hi Ever! Thank you so much! Multiple Sclerosis sickness can bring life changes. 😷 I’m so sorry that your MS affected your ability to write, draw, drive and employment. I know it is not easy. I do hope that things get better for you soon! What type of MS do you have? How is your treatment going? Did you have a recent relapse or flare-up? It may be helpful if you exercise your weak side ( Right side- Hand, Leg, & Feet) it can help strengthen your muscles and range of motion. If you have not already, maybe you can ask your healthcare team about exercises you can do to increase your strength. Staying on treatment and having a balanced diet can help too. Take some time to relax your body. 🙂🧡
I live in uk i had brain scan friday im waiting for results x i love your channel and love listening to u ❤
Hi Kim!! 😀 I’m sending you positivity and a hug from North Carolina, United States of America. I hope you feel better and get the answers you need. I truly appreciate your support! ❤️
Did you get the diagnosis?
Enjoyed hearing your story. Hope you're doing well
Hi Sonya! Thank you for your support! Overall, I’m doing well. I still have my good days and bad days. How are you doing? 🙂
Loved your video
Hi Melanie! Thank you for watching! 🙂❤️
Bless u
Thank you Gregory! 🙂
I love your beautiful accent! I love your story, glad you graduated.
Hi Javon! Thank you for your support and watching my MS story. Lol, my I guess my North Carolina accent was noticeable. 🙂
@Sierra C. Hairston it surely was dear! Hope you're doing well. Look forward to more. I did subscribe to channel.
@@javoneldridge8046 Overall, I’m doing well. I have my good days and bad days. I look forward to putting out more content! Thank you for subscribing to my channel! 🙂
Great vid, appreciate the info, thank you.
Hi! Thank you so much!! I'm glad this video was helpful. 🙂🧡
thank you i am going through the proces
My pleasure! 🧡 I’m sending you positivity and a virtual hug? How are you doing? How is your MS going?
to be honest, it is so hard i have been non-stop crying and also dealing with the symptoms at the same time, i have a an unhelpful mother who says it will probably be nothing even though neuro wants to see me urgently and i get numbness in my limbs, burning, pins and needles, electric down my spine when my put my head down. sucks super bad, thank you for making these videos it really touches so many people to see the process and stories. @@sierrachairston
I know this is an old video but i just seen it and i gotta tell you im going through a lot of similar things you went through. I dont know if i have MS but i do have weird symptoms, like my hands and feet get numb, my face i have dizziness everyday for 6 months and doctors havent been able to figure it out, i also have acid reflux and i often feel like im choking.. blurry vision, i have really bad fatigue i could barely walk and i get the shakes a lot.. havent had a brain mri yet im waiting to see a neurologist..
Hi Yeya!! I'm sorry that you are experiencing those symptoms. I can't imagine the discomfort you feel. I know you are concerned. I'm glad you went to the doctor. Sometimes, it takes several doctor visits to find out what is happening. Continue to advocate for yourself so you can get all the exams to address your concerns. As you wait to see a neurologist to get your MRI, make sure you document your symptoms in a notebook or journal because it's a tool that can assist you and your healthcare team in managing your care. I hope you get your concerns addressed soon. Take some time to rest and relax. I'm sending you a virtual hug!!🙂❤️
@@sierrachairston thank you! I will update when i get answers
@@yeyarodriguez6636 You’re welcome! Sounds good! If you need to reach out to me for any additional support this is my email address info@sierrachairston.com
I have all those same symptoms exactly for about 8 months 😢 doctors can't figure it out either
@Katie Cloessner Hi! 🙂I'm sorry it is taking some time to find out what is happening with your body. Keep documenting your symptoms and schedule appointments with your healthcare team to address your concerns. Continue to advocate for your health. Don't give up! Have you received any imaging?
I have to be in relaxed environments, if not it seems like everything spirals outbof control
Hi! Being in relaxed environments can reduce stress, anxiety, and improve your overall wellness. Thank you for sharing! 🙂
Thanks for sharing!
My pleasure! 😊❤️
Thank You🧡🥊
My pleasure!! 😊🧡
Thanks for sharing! When you speak of the numbness, when it happens, is it temporary or does it last for a while? I wish you all the best! 🥰
Hi! When I was first diagnosed with MS, I was in a full relapse and experienced numbness all the time. My symptoms would not ease up. In my remission stage, numbness can last for 15- 30 minutes or if I'm having an MS attack for a couple of hours. Thank you so much for your encouragement! 😊❤️
@@sierrachairston Thank you for your response! I hope you continue to be well.
God bless you. You're so strong and beautiful. Stay strong. God loves you. Jesus loves you.
Hi! I truly appreciate your support! Thank you for your encouragement. God is so Good! 🙏🏾🙌🏾😇
Hello, first, big hug.. could you please explain how GERD symptoms can correlate with MS? Thank you!
Hi Debbie! Big Hug! 🤗 There is a lot of interesting information on the internet regarding MS relations to the digestive system. One of those reads is in the link below, a study regarding Syndromes in Multiple Sclerosis and Gastrointestinal Symptoms. However, it will be best to consult with your primary care provider, neurologist, and healthcare team to receive medical consultation. I wish you all the best!
Adding to the Burden: Gastrointestinal Symptoms and Syndromes in Multiple Sclerosis www.ncbi.nlm.nih.gov/pmc/articles/PMC3791579/
I have multiple sclerosis n its difficult....balance problems...brain fog...difficultly finding words etc
But now i also have degenerative disease n my cartilage on my spine is depleted
Sooo the bones on or between the spine r pinching the nerves
Hi! 🧡Thank you for sharing! I’m sorry you are experiencing those symptoms. I know it is not easy. What helps you get through it?
Trying to explain MS can be crazy. Glad I did not hay in college.
Hi Bernard! I agree. It can be difficult to explain MS because every person with MS experiences different symptoms. Some days are good, some days are bad.
I had MS symptoms during college, I thank God I did not have a relapse while attending college.
How are doing? How is your MS?
@@sierrachairston ruclips.net/user/liveq8T6tSYaEgA?feature=share
I'm supposed to have mine removed soon too
Hi! Are you getting surgery to remove your gallbladder?
Hello Miss. Seirra.
Íve been dealing with this for going on 7 years. Ok I'm 38 And it never gets easier. How long have you had it an how old are you?
Hi! I understand what mean, living with MS can be a difficult at times. I was diagnosed with Relapsing-remitting MS in April 2016 at the age of 25. I’m currently 31 years old. 🙂🧡
Have you ever had muscle spasticity or spasms because i had eposodes and they only last for a minute but it sucks
Hi Jaroyne! I’ve experienced muscle spasticity and spasms randomly. My muscle spasms have lasted for minutes to hours. You are right. It sucks; it is excruciating! What helps ease your muscle spasms?
It really affects your Ms when you have a infected area of your body
Hi! 🙂 Yes, I agree. Early in my MS diagnosis, I had difficulty walking and would fall a lot. My legs felt weak, numb, and achy all the time.
@@sierrachairston I have not had an MRI for my Ms probably since 2019 I am due for another one
@@sierrachairston I have had a problem with my legs lately and tremors where I really haven't had this problem since my last relapse in 2015
Hi! 🙂I understand. Yes, it may be time to see your neurologist.
Hi I just watched your video I didn’t understand what was a mess my left leg shakes when I will walk I didn’t know what that was I get numbness in my hands tingling and my body all these things or no I even get it Tania land feelings and my leg it goes all the way up and sometime I feel dizzy and the morning I still don’t know what is going on so if you can help me put some lake to this I will appreciate it my neighbor says my eyes make this funny look but I’ve never seen it butShe says she knows about it and she told me to get checked out for it if you can help me with this I will appreciate it because I don’t know what’s going on
Hi Paula! I'm sorry to hear about the changes your body is experiencing. The best thing to do is write down all of your symptoms in a notebook (What are the symptoms, when do symptoms happen, how long the symptoms last, ongoing symptoms, new symptoms, etc.) and schedule a doctor's appointment to see if further testing, exams, and specialist will be required. I hope you will find out soon what is causing the discomfort in your body. I wish you all the best in your health journey🙂
Which were your early symptoms? Xx and is fevers a common symptom x
Hi Cheryl! My early MS symptoms were numbness, weakness, spasticity, headaches, and vertigo. It is always best to ask your neurologist and healthcare team about MS symptoms to be informed. Below is an interesting article I found regarding MS and fever.
Researchers Ask: Could a low grade fever be making MS fatigue worse? - Healthline
www.nationalmssociety.org/About-the-Society/News/Researchers-Ask-Could-a-low-grade-fever-be-making
Thanks for sharing your story. I am also having MS Symptoms for the past 3-4 years. In 2019 went for a brain and c spine MRI all normal and clear. This year (2023) had more symptoms went for brain, c spine, thoracic and lumbar MRI and came back all clear. Also seen a neurologist and neuro exam was normal. Went to optician for OCT Test and was normal. So very difficult, not sure if I should rule out MS or not? What would your thoughts be? Thanks
Hi! My pleasure! It is best to continue to work with your healthcare team to rule out or confirm medical conditions and diagnosis. Always document your symptoms ( when, where, duration of symptoms) and present your concerns and symptoms to your healthcare team. Continue to advocate for your health! 🙂❤️
Was mri done with or without contrast
Hi! My MRI was done with and without contrast.
@@sierrachairston in which was lesion found
Lesions are visible with or without contrast. However, MRI images with contrast provide a clearer image with greater details and can help diagnose MS, brain tumors, etc.
Girl I'm a soda head 2😂
Hey Ranique!! Lol!!🥤😂🤣 The struggle is real! 🤦🏾♀️
Hi from nyc. Sierra wish we were neighbors. I have an ms story too. I am going to follow you. How can we connect more than texting f 77 Ellen
this disease gets so old .
I'm tired of it .
Hi Robert! I understand. Living with MS is not easy and everyday presents its own set of challenges. How are you doing? Hang in there! 🙂