Being Diagnosed With Multiple Sclerosis : My Story

I was diagnosed with Multiple Sclerosis in July of 2015. It is my hope that I can bring more awareness to MS, and reach out to anyone who might be struggling with their own diagnosis. Thanks for watching!

[@joshriver7600]

Thank you for sharing ur story!! First I'm sorry u have it!! U are so positive!! U are reaching people like me and give hope and a sense of peace that its NOT a death sentence!!! God bless all y'all!!

[@jadielabdiel5921]

You prolly dont care but if you're bored like me during the covid times then you can stream pretty much all of the new series on InstaFlixxer. Been watching with my girlfriend for the last few months =)

[@yosefhezekiah4818]

@Jadiel Abdiel yea, have been using InstaFlixxer for since november myself =)

[@ehvegankitchen4707]

Your so amazing,strong and positive much thanks for sharing your story 🇨🇦❤️

[@glowholistik]

There is lots of options for keeping in remission. Massage therapy, cranial sacral therapy, chiropractor, low carb Paleo/keto type diet, positive energy reiki sessions.... They can all help with the healing and keeping of remission. Stress makes MS worst so stay away from stress. Also yoga and stretching helps me. Vitamins of course vitamins d, magnesium, all omegas and cod liver oil or flaxseed oils are good for brain. Good health ❤❤❤

[@CapturingChaos]

Thank you for all the great info! 🧡

[@AJHR77]

Thanks for sharing your story,we all have one. I had symptoms ignored until I went blind in my eye. Keep s'myelin!

[@lorraineophoff4984]

I am waiting for a diagnosis, for years, lots of tests this year especially with a Neurologist. I feel my Neurologist is very thorough, and I trust him completely. For him, I am very thankful. But the waiting is horrible, feeling in limbo is very difficult.

[@CapturingChaos]

I hope you get answers soon, the unknown is so hard 💜

[@LITBeauty]

Just came across your video. I was diagnosed last summer. My first symptom was also optic neuritis & my story is very similar! When my ophthalmologist said I most likely had optic neuritis I had no clue what that was & asked him what pharmacy I could pick up my steroids at 🤣. The second he told me I needed to go to the hospital, I lost it! Thank you for sharing your journey!

[@CapturingChaos]

Thanks for your comment, it's always so nice to hear from others!! Man it sure would have been nice to just run to the pharmacy!! Hope you're doing well!

[@lovingdale2449]

Hi, thank you for making this video, I am going through the exact same thing that you described in this video and I'm struggling with it all. I haven't been officially diagnosed with ms yet but the neurologist I have which is not great unfortunately, wants me to start on copaxone injections 7 days a week and I'm terrified. I just had a neck and chest MRI last night and the waiting for results is going to drive me crazy. I'm just so scared.

[@CapturingChaos]

I'm so sorry you're going through this!!! The diagnosis process can be brutal, hang in there. Keep me posted, and try not to worry too much, I promise it will get better 😘

[@getintoits2786]

Hey, how is it going now?

[@eileenpeckenpaugh8544]

Thank you for sharing. I myself have been on going for 2 years still trying to get a diagnosis.

[@CapturingChaos]

I am so sorry you are still trying to get a diagnosis!! That is soooo hard. I feel very fortunate that my diagnosis was quick, I know often it takes years. 💜💜💜 How are you doing?

[@Dmogul]

Great video by the way

[@CapturingChaos]

Thanks!

[@gumtree7177]

Sarah Hi 👋🏻 hope your enjoying motherhood and good things in life as I’m sure your are. Just a special hello 👋🏻 to you stay healthy god bless you and your family and your entire support team. 😎🙏🏻🌍🇦🇺 ian from Australia 🇦🇺

[@mswarriortroyedwards389]

I did the same thing when i was diagnosed and that's why I started my channel as well if I could just change one person's life or even change one person's way of thinking about the disease

[@CapturingChaos]

Awesome! I will check your channel out, thanks for sharing!

[@mahaswetaacharya]

Hey what is the treatment going on ? My fiance is suffering from this .Lost his right eye vision

[@CapturingChaos]

So sorry to hear about your fiance. To treat the optic neuritis they gave me an IV steroid for 3 days which took care of it. As far as meds, I'm taking Aubagio to manage MS.

[@mahaswetaacharya]

@@CapturingChaos you got your vision back?

[@CapturingChaos]

@@mahaswetaacharya I didn't lose any vision thankfully, I just had really bad pain when I moved my eye.

[@DiaperDelight]

Lighting may not be the best, but, nonetheless, you look marvelous! So sweet and personable, too!! Fortunately, you are still fairly young and relatively early. Time will be the key, of course, depending upon your exact circumstance and MS type. Your husband will be most important as the future unfolds for you. (Hopefully, you have developed a lasting bond while you are still this highly desirable!)

[@glowholistik]

Please search vitamin d protocol north America on Facebook. I have been on a high vitamin d protocol that has halted disease activity for me. Please look into it!

[@Brandi.65]

Did you have any tingling in your face, head, neck?

[@CapturingChaos]

I do now, but it didn't start that way. It doesn't last, but it comes and goes. It's super annoying on my head.

[@gumtree7177]

Capturing Chaos Gods care to you all. Gods intervention 🙏🏻👼🏻

[@elizabethconroy7665]

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[@elizabethconroy7665]

Nice to meet you Good luck on your Journey Gentle Hugs from Amman Jordan The Middle East

[@georgekafantaris7807]

YOUR YOUNG AT EARLY STAGE,,,WAIT AND YOUL SEE HOW SCREWED WE GET

[@CapturingChaos]

+George Kafantaris you're right, I am young and newly diagnosed. I'm very aware of what this disease is capable of, and have seen first hand what can happen. I also believe and choose to stay positive and try to do everything I can to stay as healthy as possible, knowing I might not always be as fortunate as I am now. I wish you the best, and hope you find peace and comfort.