Відео

I Have Known her for about 6 Years now, and We all Love her very Much, she gives us all Hope, shes an Inspiration to all of us who know her, If anyone can get something Done, It will be Her, She Never gives up, She Loves a Challange, That Makes her more Determin to get it done, Love You As we know you, Nee Nee Keep Going I know Your Dreams will come True, Love & God Bless you always

Spoinal cord👨🏿‍🦯me?📖

Jacob Witt goat

Inspirational

He's now walking, driving, tilling the garden, and getting back to normal! Thanks sheltering arms!

Good for you Doc! So proud of you. Love you

Dear God..give me cardiac arrest so I die in my bed..no life saving measures. Please bring it God. I'm dying any of dozens of cabcets timours masses. Have me die in my bed of cardiac arrest. Please i beg of you.❤🎉😊

Go Cassie❤️❤️

Such amazing work done here!

I was diagnosed with CIDP back in 2007. Ive learned a lot since then and am living an almost normal life again. A few tips to help anyone dealing with this disease: A keto style diet works best for me. Lots of organic healthy meats, veggies and fruits. I tried a vegan diet but it made it worse. A diet of good fatty meats, eggs and avocados is good because it helps to regrow the myelin sheets that was stripped off the nerve endings by the immune system. Cut out all processed food especially sweet foods. Sugar is your number one enemy. It’s best to avoid all forms of sugar even stevia etc. you may can get away with a “little” manuka honey. Avoid smoking and drinking any alcohol, including wine. Exercise as much as possible and lift heavy weights (at least what is heavy to you). This will keep you stronger than the disease itself. Workout your entire body especially legs and arms. This is how I regained my balance. Get plenty of rest. When showering. Switch from hot to cold to stimulate your nerves, ending your shower with cold. Get a vibrating foot massager to stimulate your nerve endings in your feet. By doing all of these things I am 90% back to normal without taking any steroids or ivig, haven’t been back to my neurologist in ten years after he told me I will be wheelchair bound if I stopped the treatment. I’m not advising you stop treatment I’m just saying that’s what I did. I didn’t abruptly stop, I slowly reduced the amount of steroids I was taking and weaned myself off of them as I was doing everything I wrote in the comment. The stronger I got the more I weaned myself off. Hope this helps someone

LOOK AT GOD. PRAISE GOD YOUNG MAN. THANK YOU JESUS, THANK YOU😂

Am in South Africa, please help me locate your rehab centre ! I have a C5 from car accident in January 2020.

More a plug for this facility than Antony story

I'm blown away. A brown recluse spider can do THAT? My God.

Thats my big brother❤️🥺

Sir, you don’t know fel I am spinal cord injury😢😢😢😢

Cute marketing video for this place. I am afraid that reality works a little differently. I am a mTBI survivor. I did not receive much care at all. The few docs I visited were not helpful at all. This is not uncommon either. I am not saying that quality care can never be helpful- it can be. Ultimately however, it often comes down to luck, nutrition, reducing stress, inflammation, time and did I mention luck? Over TIME, some can finally begin to do more things that help with neuroplasticity. For example, play an instrument or bounce a ball when you walk. This can help. For a while, I could not tie my shoes or play a note without getting tired and fatigued. Now I can...but it took years. I now look back and realize a lack of quality sleep was behind a lot of my issues. As that improves and you are able to think more clearly and get in some quality exercise, and start to eat better (healthy FATS), and a few key supplements, things may improve for some of the luckier people- sadly, not for everyone.

Love you dad! Keep pushing! You’re doing great

How is GBS or it's cousin CIPD diagnosed? I have neuropathy below my waist that feels like GBS. I've seen army of doctors and specialists over the last 9 months. X-rays, CT scans, EKGs, MRIs, nerve conductivity studies, etc, etc. No diagnosis at all... So frustrating. Maybe they are hiding the dignosis due to my advanced age. GBS takes months even years to treat, and that costs money. I went from being 100% mobile to unable to walk. My legs feel like concrete blocks.

Thanks for your comment.

Congrats, George. This is such a heartwarming story. You are such an inspiration to so many. So very proud of you.

What a crazy and sad cause for a csi. Wish you a good recovery

❤👍🏽👍🏽👍🏽👍🏽

Véŕy good

'PromoSM'

I had a hemorrhagic stroke due to an AVM, I'm walking but my arm still paralyzed, still working on it. I see more videos of people with Ischemic strokes.

I knew I didn't like spiders. 😬

Your courageous efforts & through faith in God had made you to recover. My wishes for you to lead a healthy life.

Praying for your recovery. God bless

ua-cam.com/video/gMuStEhP3IY/v-deo.html

I hope and pray to you and your family for good healing 😔🙏

God bless u young man

Awesome. Never give up…

That's so inspirational to watch. A brave young bloke and a dedicated team of caring professional working together to get him home to his amazing family- and fishing of course x

Awesome! Keep fishing!

Thank u so much my mom is doing the parallel bars now slowly recovering thank u god