I met Deshon at his workplace. His determination is nothing short of amazing. He is an extraordinary young man, with an tremendous personality. He made my day a better day. Be strong Deshon…may God bless you in your battle with this illness.
I had the honor of meeting Deshon today with my granddaughter. He was so very helpful and genuinely wanted to help me find what I was looking for. He shared his incredible story and that it was on RU-vid. I told him that he is one special man and that his Heavenly Father needs him to be here to share his story. He hugged me twice and we gave one another high fives a few times, I told him that I would see him again. The Spirit was so strong when I was talking with him, I was meant to meet Deshon today! What a wonderful day….on the Sabbath❤️❤️❤️❤️❤️
As I sit here and watch your video tears run down my face and it’s because I know of everything you’ve gone through because two years ago my daughter was diagnosed with NMO and everything you experienced she has experience it, she lost her vision in her left eye first then her right eye, there is so much to say but I will just sum it up with God is faithful she doesn’t have the pain in her body anymore and she’s able to walk now but she hasn’t regained her vision yet but I know that there’s nothing too big for God and with him all things are possible he’s faithful to his promises.. be and stay encouraged and know that God is a healer and he will never fail you .. God Bless You
I was Blessed today while shopping at Lowes! Meeting Dashon was a n awesome Blessing and the sharing of his testimony just made my day. He went above and beyond while helping me and I really appreciate it! Lowes aught to be commended because while he was helping me one of his coworkers Terry had came out just to check on him. That Blessed me to see the love and concern for one another! TGBTG!!!
Deshon is an inspiring young man with a heart of gold. Thanks to all who put the work in to help him. He’s a hard working young man who keeps fighting. I met him at Lowe’s in Cartersville. I see him in there all of the time, in the garden section. He is always positive, helpful and cheerful. It’s a pleasure to see him in there. On a slow day he told me his story and it lead me to this video. My heart goes out to him and all who have to deal with this. God bless and keep him.
Desmond it was very nice meeting you at Lowe’s Sunday. You are a very nice young man. It’s a incredible story, glad your getting the help you need. Your in our prayers 🙏
It’s hard I woke up randomly parylzd from the neck down 4 kids I was In icu for 6 months for me to start walking and using my hands again I lost everything my hands don’t open all the way and my whole body feels numb. This thing is so hard painful I cry everyday I hate it always have to find To keep my mind busy
Thanks for sharing your story with me today Deshon trust and believe in our merciful God to bless you plentifully through your journey 🙏🏾 PEACE ✌🏽 My Brother.
Deshon, thank you for sharing your story with me, I am so glad to see that you have such a beautiful group of caring and supportive people and great healthcare team members. I can truly see how far you have come! Thank you so much for your help today! I admire your spirit, and your great customer service! Bea
You're very very welcome Bea it's been a very tough road and experience I have ever encountered. 😢❤ I really definitely want to help a lot of people as best as I can, that is exactly why I have decided to go PBS. 🥹
Oh no, I'm very sorry to hear that... Did you go to the hospital and thought you was going through a pinched nerve? Because my reasoning of asking because the exact same thing happened to me... 😢😮💔😞
So sorry to hear, my husband was very I’ll with NMO/MS - we use Dr Wahls protocol for autoimmune conditions and he has improved still fatigued no numbness and vision is better! Best to you!!
I'd love to know the treatment. I fell sick around August 2021 by November 2021 I was completely disabled. Diagnosed with nmosd in February 2022. But I am seronegative. I've been on Ocrevus q6 month infusions and 3-5 day solumedrol infusions for flares. I'm not getting better. Only worse and I'm missing out of my entire life. They want to try Acfhar self injections now. Other than that I just feel and know I'm a goner. This is a horrible disease. I'd never wish it on anyone for even a 5 minute walk in my shoes.
I'm so deeply terribly sorry about your diagnosis... Yeah I must say, it's not fun at all it just makes you feel very defeated and out of place .... I am so going to pray for you and really hope you get the kind of treatment you truly need and deserve. 🛐💐😇
@@annahLadams you're so very welcome, I know things can be kind of tough right now thus far because I'm currently kind of dealing with my diagnosis myself, so I know exactly the feeling I really pray for us to find our best recovery possible 🛐💐😇
Deshon & Anna you’re both in my prayers💕 Deshon, it was such a pleasure to meet you. You’re such a beautiful, courageous soul! You’re a light, so full of positivity. You truly blessed me today with your sweet spirit. Thank you for helping me today, you truly amaze me! For you: Jeremiah 29:11 For I know the plans I have for you,” declares the Lord, “plans to prosper you and not to harm you, plans to give you hope and a future. Paige
Oh no, that is so terrifying one of the things I hate the most is someone who is suffering I am so definitely I'm going to pray for your mother and she gets the kind of treatment she needs in Jesus name I pray Amen 🙏🏽❤️🥹💐
@@deshonwilli93hi darshon am vaishakh from India. I need to talk to you. Am also a patient of NMO. May I get your WhatsApp no, or Instagram Id. Friend, I really really want to talk to you
Thank you for sharing your story I to have NMO. I am moderately paralyzed from the waist down. I was First diagnosed with transverse meylitis then a year later NMO, a struggle of 6year now. I like to say 3 years of decline & 3 years of positive progression. My story is to long to go into, but trust me i am muuuuuch better from where I started. Your video is motivation to me, to get up and work that much harder to continue to eat healthy, workout, & to stay Address to new technologies. I am sure there will be a cure one day. Again thank you for sharing. For those that my want to know my treatment. ( keep in mind these Doses were higher at 1 point in time. But giving the positive progression have been lowered. And this is where I today. Rituximab treatment- 3times a year 2 in June 1 in Dec. Mycophenolate 500mg every other day. Baclofen 20 mg 3 times a day I was on Prednisone for about 2yrs. But given my progression was able to come off it a year ago! To all that are fighting this disease dont give up. I know the mental battle can be harder then the physical at times. I pray for your progression, peace and strength ❤ Jermaine Smith
Oh no, I'm so terribly sorry to hear that God bless you, I'm pretty sure you felt very defeated and down God will always help you through this very tough journey because I felt exactly the way too.I completely understand exactly how you're feeling right now... like defeated, out of place, and helpless. 🛐😞💔 I really hope and pray you get the type of treatment and help you truly deserve. 🥹😊🙏🏽
Yes, especially newer drugs made explicitly for NMOSD. I have soliris infusions every two weeks and that's the only medication I'm on now because of the soliris working so well. I got off steroids, baclofen, and some other meds. It was slow to work, felt better after six months, and each month after that I felt better and better. Symptoms faded, although I still have a bit of MS hug some days and skin sensitivity on only one arm now, and sometimes my stomach. I walk a little wobbly briefly after sitting for a while but then I'm steady. It's a hard journey but the Soliris really helped me to get back to as normal as I can be, no spasms/seizures, electric shocks going up my leg, no numbness etc. I always thank God, the VA hospitals, and everyone who helped me in my nightmare. I hope you can get the immunosuppressant that will work for you.
@@DreamingDarlin what is soliris? I was diagnose with NMOSD too about 1 week ago they gave me 5 steriods shots and now i feel better and better everyday although the numbness still there . Also i want to ask did u ever feel itch around your body?
@@melchieempiales5749 how are you now? My sister diagnosed nmo. She is on steroids and inj rituximab 1 month ago. What about ur progression of disease.?
@@melchieempiales5749Yes itching comes from the nerve damage which is what I was told it can be irritating I feel at times I’m about to scratch my skin off.
