Multiple Sclerosis - Walking/Stairs - I’m thankful for the challenge.

[@jomamapalmer9223]

You’re amazing!! You don’t give up n won’t give in to MS! I’m right where you are in my gait. It’s crazy becuz what you do, I do; bend forward, shuffle, etc. But I too am not stopping…MS is said to make you weak n mess with your brain function. But I say, MS has made me strong 💪 n I am determined to move forward n never stop!! We are NOT our circumstance and by the Grace of God, He’ll see us through this. He’s the Great Physician n nothing is impossible with Him🙏 Thank you for sharing, you encourage me.

[@lizmorgan5463]

Watching you today as given me so much inspiration ,I've got parkinson's, and I get angry ,and think why me ,,but i had a good life, I'm 74 ,,,and now I thank God,,,,,bless you and your family,,

[@denisek292]

Wow, you’re very impressive! As someone with secondary progressive, and with major falling issues just getting out of bed, I’ll admit I was anxious watching your video. You’ve given me hope PT can restore my ability to walk. Thank you for sharing!😀

[@summersuetholz7884]

This is so amazing. What determination and mental strength... Just wow

[@stevecolvin1650]

And yet every single time I walk into your business I'm greeted with that great smile of yours. You're a Beast.

[@willpan6659]

Keep going man! This is amazing don’t quit!! Be mobile stay mobile keep moving! You got this!!! I miss being able to walk like this Don’t quit!

[@kathylopez1336]

Very good I too walk just like you and you are a source of encouragement to me sometimes I just want to give up It's unfortunate that my MS has caused my marriage to be in trouble Because my husband can't believe how much I have changed and he gets alarmed when he sees that it looks like I may be getting worse

[@brianschmitz2163]

Thanks for posting this. 💜 I have similar movement issues and felt every awkward motion and understand why you do it. I too, often wonder how I appear to others. This video helped me understand that better.

[@Aim4God]

Watching this was inspiring and motivating. Thank you for sharing this! May healing come to you and everyone here!

[@shawnmcanthony5724]

I ❤ you

[@janehouska3605]

Keep moving man! Well done! I’m right there with you. Everyday is a new challenge. StY strong 💪💪💪

[@joesiders7388]

Thank You so much for sharing this. Should be proud of yourself!

[@NeilBradleyMS]

I can totally relate to your mobility issues, so sorry. Hope things have improved since shooting this video.

[@Ms.Tucker89]

I WAS DIAGNOSED WITH RRMS IN APRIL 2021 & I CAN RELATE TO THIS SO WELL... FEELING LIKE YOUR ABOUT TO FALL LOOKING FOR SOMETHING TO LEAN ON OR JUST TOUCH... FEELING LIKE MY WHOLE BODY WAS JUST COMPLETELY FOLDING OVER I WAS EXPERIENCING DROP FOOT AS WELL TRIPPING OVER MY OWN FEET... BUT THE HEAVY LEGS ONE DAY WEAK THE NEXT & BALANCE HAS TO BE THE WORST... I HAVE BEEN ON AMPYRA FOR 6 DAYS NOW & THE IMPROVEMENT I SEE THUS FAR IS AMAZING... I HAVENT BEEN ABLE TO MOVE AROUND OR STAND IN MONTH'S LIKE I AM AFTER TAKING AMPYRA! MY ENERGY IS UP, I WAS IN A DEEP DEPRESSION & I'M GLOWING RIGHT NOW! I LIVE ON A HILL & MY LOCAL STORE IS AT THE TOP NOT A LONG WALK BUT LONG WITH MS SHIT IMPOSSIBLE... BUT TODAY I WALKED UP & DOWN THE HILL WITH NO PROBLEM! PLEASE FOR ANYONE WHO READS THIS & HAVING WALKING ISSUES TRY AMPYRA!

[@denisek292]

Thank you for the suggestion. Surprisingly, I heard about it over 10 years-ago, but just started falling as soon as I get out of bed. Tired of being eye-level with my Westie, who looks at me like I’m nuts!😂

[@sheridanrose9880]

I have Primary Progressive and I can totally relate to your post! It’ll be easier to show to my doc! Thank you!

[@aletheia25]

Bravo Joe! Coraggio! Continua così. Saluti dall'Italia

[@linnpennell6102]

You go buddy. I have MS as well and that's what it's like. I tell people that I'm not drunk. I have MS.

[@sushmasharma-jh1cl]

I was diagnosed year ago...I have started cycling ..and it has helped me a lot..grt...u keep us motivated ....

[@aurelienmatthews6511]

I am like this. I was diagnosed with multiple sclerosis

[@larryhayez]

I'm just like you the neurologist told me to use them or lose them keep going man

[@davidjustdavid3955]

Hello from Melbourne Australia. I have GBS and recently had covid which had made the condition worse and can relate to this video . I hope your condition had improved and i look forward to your story of improvement. Staywrll and God Bless

[@jg102xc]

God bless you, too.

[@johnjkizer6399]

Your doing amazing, keep up the hard work, I know there are good and bad days because I am a quadriplegic and deal with the same issues, God bless you

[@jg102xc]

God bless you, too.

[@shawnmcanthony5724]

Wow you have great determination.I have had ms since i was 21 i am now 48. Going to the gym helps. Now using a cane a month ago.My wife encouraged me to use one

[@1rosabonita]

You did a great job you did all your effort think positive bring it to Jesus Christ to heal you and I believe and step in Faith Amen

[@billiemarie7078]

A few days ago i started walking very similar to this im waiting to get another MRI to see if i have MS.. stay encouraged❤💯

[@idraculaa]

Same for me, my first MRI showed nothing, waiting for more results. All the best for your journey ✨

[@billiemarie7078]

@@idraculaa thank you peace and blessings to you

[@Garpot]

@@idraculaa how are your test results? I was diagnosed June last year...Stay strong!

[@Garpot]

How thing with you? Any update? Stay strong!

[@kathylopez1336]

Pls try to walk on a regular basis, I believe that if I would hv kept my regular walking up I may hv not been so badly affected as I am now, but I'm not giving up

[@VerbalOnLife]

Wow amazing challenge. Good work and keep walking!!

[@usualobject0]

This was me 2 years ago...sending you prayers 🙏

[@jg102xc]

Thank you! I hope you are doing better.

[@traceyl9959]

Are you better, if so what did you do to get better?

[@paullaw6988]

@@jg102xc Hi Joe Gagliano, how are you? I will pray for you to get better soon. God bless you!!! Hope you doing well. Kind regards, from, PaulLaw.

[@Ms.Tucker89]

OH GOD THIS BREAKS MY HEART BECAUSE I KNOW ALL THAT HE IS FEELING PHYSICALLY & MENTALLY

[@toddmilligan6603]

I have to use a walker or cane unless there are walls or furniture close by. Good video.

[@Tns85]

I was dx 5 years ago. Keep moving, it helps a tremendous amount

[@jg102xc]

Teresa Nigro this summer will be 21 years for me. Staying active is definitely good. Just don’t over do it. I have multiple times over the years and paid for it.

[@Tns85]

@@jg102xc i know what you mean. I had a horrible relapse last year and was out of work for 10 months

[@paullaw6988]

@@jg102xc Hi Joe Gagliano, how are you? Keep up your practising your walk and exercise everyday. Keep moving, it helps a tremendous amount. I will keep you in your prayers. You will get well and better soon. Kind regards, from, PaulLaw.

[@wendywebster5920]

Tada! And you are the top of the stairs. Well done, sir. I know how this feels, though I am not as far as you. Though climbing stairs indeed feels and looks like one is going up the stairs on a moving ship (in a decent storm). Been there plenty of times. I am glad to see that my house is mostly ground level. The stairs to the attic is quite narrow, so it doesn't give me much room for the potential "falling over". Keep going!

[@sweetmama6314]

I use imagery where I see myself walking in my mind's eye. The stairs, you are brave running man. 🏃‍♂️

[@Themsmystorypodcast]

all love

[@Garpot]

Joe - how are things with your MS? I feel ya...my MS very similar to your walk my friend...stay strong...you have a lovely family and friends for support!

[@theluckyman74]

I, have been dealing with walking issues, for over 5 years now, and really, have no idea, what disease, I have, because, my overpaid doctors, refuse to send me to a Neurologist. My gut, is telling me I probably have MS, but can't say for certain. Today, I, had a horrible day, walking around just as bad as yourself. Keep in mind, I am also dealing with parathyroid disease for the past 6 years and, found a surgeon in California, that is going to operate free. I, also had, a heart transplant on Easter Sunday April 15 2001.

[@drpixels4728]

Keep moving... prayers and love

[@zeronim1]

Exactly like I use to walk two years ago! Keep going bro!

[@zeronim1]

Also if you want to talk I'm up for it

[@jg102xc]

@@zeronim1 how are you doing now?

[@zeronim1]

@@jg102xc doing much better after being in contact with an Irish doctor. High d3 and the right form and dose for you

[@ScareBearGirl]

im starting to walk in a similar way, its very jaring. Waiting on Getting a MRI rn

[@daveolep7657]

It take about 1 to 3 months for the tumeric and black pepper , kale , bitter melon ,cilantro , parsley to work stay blessed God bless you .

[@jg102xc]

God bless you, too.

[@vanessapalacio8756]

I saw myself in this video thank you for sharing.

[@cristobalrodriguez8693]

Proud of you

[@mmemichelle2325]

Looks like me... I know how hard that you are working!

[@Sonyakparker]

I haven’t been able to get a DX yet. But I have very similar symptoms walking too!!! I have had child service called on me saying I was drunk all the time and doing drugs. Thank goodness I keep a copy of most medical. Keep your head up I live in NM and we have some crappy drs. I am fixing to go back to UNM again and they want me to go to the mayo but insurance is having a difficult time agreeing. Thank you for ur share of your walking it helps to know your not the only one. Blessed be

[@sewlovemydogs]

Ask for an MRI from your Dr or a referral to a neurologist as soon as you humanly can. The longer it takes for you to begin medication to top the progression of MS the more compromised you will be. You can’t get back the mobility you’ve lost, but the MS medication will stop it in its tracks. I wish they’d realised I had MS sooner. Please take my advice, I’m not an authority on anything, but I do know this. Take care. Act now.

[@Sonyakparker]

Heidi Newbery I have seen teams in major hospitals here in NM and Close to me in TX. In 6 years I can’t tell u how many MRI I have had for muscle weakness and optic neuritis. Have had more than 6 lumbar punctures muscle biopsy lab work and so so many hospital stays. Here they pretty much say idk what’s wrong it points to MS with out clinical findings. I have tremors so bad and walking problems I now threw my insurance I have a care giver cause it is difficult for me. Old what to do any more.

[@sewlovemydogs]

Sonya Parker are you seeing a neurologist

[@Sonyakparker]

Heidi Newbery yes but he has stated the same thing and wants to send me to UNM here in NM. I don’t know what else to do.

[@theadventurekidz-scienceho843]

I have flares on and off and walk like that but my balance can be worse. I feel like it’s something going on in my head when this happens. Worse with activity

[@karenfuhr1]

all the love to you.

[@ObamAmerican48]

Way to power thru, man.

[@byron2521]

I have MS, his motions are like looking in a mirror. going up steps is one of the hardest things for me. Sometimes I have to get on all 4s if there is no rail.

[@Ms.Tucker89]

JOE CAN WE GET A UPDATE !

[@Tns85]

You got this!

[@gabbyfranks78]

Keep your head up. I've been curious about Ocravus. I heard its making MSer's walk again.

[@jg102xc]

Gabby Franks I’ll be getting my second dose fairly soon. Hard to say yet but I’m better than I was, so far.

[@gabbyfranks78]

That's great. I hope you see major improvement each round. Do you have side effects if so what are they? I wanna try this. I've heard nothing but good things from others. Good luck

[@jg102xc]

Gabby Franks the first dose was split in half but it didn’t bother at all from what I remember.

[@sewlovemydogs]

Please tell me what this is, does it help with fatigue? I’m in Australia and haven’t heard of this drug.

[@jg102xc]

@@sewlovemydogs I’ve only had two doses so far. I’ll do a follow up video fairly soon.

[@IamCurrentlyAscending]

I spent my January like that. I've been there and I know how much it sucks. But I also know how much it takes to do all that, hats off to you my friend. MS can kiss my ass.

[@Ms.Tucker89]

THE DRUNK WALK UGH! BEFORE BEING DIAGNOSED WITH RRMS I WAS HAVING WHAT I KNOW NOW AS SYMPTOMS & I WOULD BE TRAVELING HOME FROM WORK ON PUBLIC TRANSPORTATION & PEOPLE WHO BE LOOKING AT ME BECAUSE I LOOKED CRAZY I LOOKED LIKE I WAS DRUNK & WAS SOBER COMING HOME FROM WORK! AS A FEMALE TRAVELING I STARTED TO FEEL LIKE A TARGET LIKE SOMEONE WOULD TRY TO TAKE ADVANTAGE OF ME THINKING I WAS UNDER THE INFLUENCE 😩🙏🏽 I HAD TO START TAKING UBERS SMH

[@pennsyltuckyreb9800]

I'm currently awaiting an official MS diagnosis. Still going through all the testing. I do have 3 lesions on my brain and 3 mysterious non-cancerous tumors (hemangiomas) that popped up out of nowhere. Past month my walking gait as been severely affected. I'm not as bad as the video above...more stiff style if that makes sense. Anyway, I always get looks now like I'm a crazy person, drunk, or get that "dafuq is wrong with you?" Stare. Sucks.

[@gwenniewennie8325]

Im walking like this now. Im having a relapse. I see my doctor on friday any way so i hope it doesnt get worse ny then.

[@indie5826]

I get what you are going through, the only change I would say is , save some energy and go straight upstairs and hand on the banister first on youf right to be safe.

[@codycommentsonvideos5755]

Ive been having a lot of balance problems. I now hate walking because my legs always hurt a lot afterwards.

[@JujuBey-s9p]

You're doing great

[@IZZFC7]

Thank you for sharing.

[@hanskrieger8674]

Wonderful

[@abee2685]

It has helped me considerably to have a rail up either side of my stairs so on bad days I can almost pull myself up them. Could you attach more up your walls the whole way? Best wishes to all fellow sufferers.

[@jg102xc]

We sold that house last year. I don’t have to use any stairs in our new house unless I want to go downstairs..

[@ChristopherJohnson-q5d]

This is my gospel stand 👨🏿‍🦯

[@daveolep7657]

A lot of tumeric the fresh one an al lot of black pepper . Bitter melon , kale , olive oil .

[@debbiramsey4603]

The Sago Mine Disaster victim had lost his myelin sheath on the limbs in the disaster times, they gave him fish oil and he regret them hich I be never hard of and I'm 69" so you know what I'm thinking.. am I wrong but us multiple s some how relaTed.. ..I can't recall. Just a thought anyway. Prayers for you. I've had co workers with it. I'm nobody. I'm just thinking out loud, I'm probably way off.

[@1rosabonita]

he needs to use a walker So he does not lose his balance,and don't get hurt,there is nothing wrong using a walker

[@chriswilliams7824]

Great achievement warrior. With MS every action is a grand gift. Have you tried the Terry Wahls Protocol/diet? Her routine has proven effective. I've yet to try it. Her interviews are useful though. Stay💪 and🥗.

[@jg102xc]

Yes I have. Not currently following it but my diet is very strict. It has helped me a lot.

[@АннаАннова-ц1в]

МОЛОДЕЦ! Привет из России!!!

[@kahdijahali8022]

💪🏻

[@josephmalter670]

This guy looks like me and walks like me AND his name is Joe!

[@baronghede2365]

If you find my comment: speak to a chiropractor, try Herb's like turmeric, ginger, and Asian ginsing and try the Mediterranean diet, Blessed Be.

[@baronghede2365]

Look into lions main mushroom.

[@joshuawinne]

Do you still feel like you are getting better or worse?

[@jg102xc]

Joshua Winne the last year has been a roller coaster. I get worse, I get better, worse then better.. I’ll be putting up more videos, soon.

[@joshuawinne]

My mobility is about the same as yours but I am like that all the time. I just had to stop working and am currently applying for disability. Good thoughts your way my friend

[@jg102xc]

Joshua Winne sorry to hear about your struggles. My level of difficulty to move varies but this is what it is and has been for a long time. Wishing the best for you and yours, too. God Bless.

[@kmg2497]

Sometimes I feel like I’m the only one who struggles with these issues . Some days are easier than others. Stairs: Haven’t quite figured out a good way to do those yet! Thank you for being brave enough to share this video.

[@paullaw6988]

@@jg102xc Hi Joe Gagliano, do you still feel like you are getting better of worse? Wishing you the best and your health. God bless you!!! Good thoughts are on the way. Kind regards, from, PaulLaw.

[@عارفاللهيبي-ذ8ح]

Just like me l have ms to

[@markhetz1119]

Is it painful

[@jg102xc]

I've been thinking about how to answer this for awhile. It's complicated. I think a video will be better. Talk soon..

[@markhetz1119]

@@jg102xc 👌🏻🙏🏻

[@davidalbro2009]

[@joshuawinne]

Do you know Jeff Campbell?

[@jg102xc]

Joshua Winne yes.

[@joshuawinne]

@@jg102xc I'm orginally from Auburn too. The Campbells were a family friend growing up. I was going through some of Jeff's texts back and forth were he wrote your name and said MS. Sad about Jeff, he was miserable though. I hope he found release.

[@jg102xc]

@@joshuawinne poor Jeff. I’m sad he’s gone but happy that he is now free.

[@joshuawinne]

@@jg102xc how you doing man?

[@sabtrsabtrov4067]

Молодец привет из Украины

[@roshanijamodkar3082]

Ayushprana Aayurved At Kerala for MS

[@Ruth_T]

Does this come and go or is this constant?

[@jg102xc]

I’ve basically been like this since the very beginning. It wasn’t this bad early on, it’s just progressively gotten heavier and more stiff over the years. Some days are worse than average and some are better but always a struggle/not being comfortable.

[@Ruth_T]

Is this painful for you?

[@jg102xc]

Minus never being comfortable it’s more frustrating than anything..

[@Ruth_T]

@@jg102xc are you taking anything for it? I get spasms in my legs but they are painful and they put me a muscle relaxer which helped a bit but I still get the tightness which to me is weird and uncomfortable.

[@jg102xc]

@@Ruth_T I’m currently taking Ocrevus. I just had my 3rd dose a couple of weeks ago. Leg spasms drive me nuts, too..

[@Ruth_T]

@@jg102xc I haven’t been diagnosed with MS I just get very bad spasms in my legs and I work on my feet and it disabilitates me to the point where I had to go to the dr. But they aren’t doing much. It came to the point where I had to cut down to work to 20 hours a week because I just can’t be on my legs that long. But for me it’s painful so idk I’m just curious I wish I knew what was going on

[@jg102xc]

@@Ruth_T I wish you the best. Keep in touch.