Відео

. . I am a BSc nurse... Because of MS... I didnt getting the chance for work my dream country 😔😔😔fait... that was my ambition 😔😔

With stays does the support worker get any payment for activities on the stay

I researched and found that there is not a single video of you in the search results of UA-cam. Not in the search results means that if you search on UA-cam by writing your video related keyword, other people's videos come up but your video is not found. And that's why your videos are not being shown to the desired viewers. As a result, your views and subscribers are still so low. To bring the video to the search results of UA-cam, you have to follow a few steps, and as an expert, I can play an effective role in solving this problem if you want.

Yes Natural Mindfulness course im doing training with is aoa Shinrin-yoku ie- Forset Bathing

Yes I am currently doing a Natural Mindfulness Guide course

Scottish Lochs surrounded by woodland my favourite nature areas

I feel connection to nature in Forest and even better with water thru it

Im from Montrose, North East Scotland, UK

Is is wise to give a support coordinator consent to talk to ndis or ndia on on your behalf.

*Promo SM*

Wow,this is a holy grail

I am wanting to get into support coordination and while I am already doing an online course, I find this presenter and webinar to be excellent! It is to the point, easy to understand, well-laid out. Thank you for uploading this 😊

I just really wish there was a video out there. That would show what it's lwhen you're having spasms I don't know what's going on with me up. I am progressing no allegiance on the brain. But I have constant spasms in my feet legs I have tremors as well. I've been diagnosed with fiber ayalgia oa and my joints, we're not sure what else is Going on but kaiser is horrible I've been having progressive symptoms of whatever's happening for the past five years. I'm always in pain thank you for sharing your story

My neurologist said exercise is even more important than medication he might be right i still walk but with a cane . I do squats and weight training daily have had ms for over 20 yrs

Mavenclad may be listed as "moderately effective" but it changed my life for the better...almost like it completely took away my MS So thankful for Mavenclad and its minimal side effects

I have MS, I’m almost 50 and still have regular periods. I have been noticing off and on for the past 6 months I feel unwell in the evenings. When I feel unwell I take my temperature it will be between 38-39°C. I generally feel cold when this happens and I haven’t noticed any hot flashes yet. I’ve also had bloodwork that doesn’t show any infection. Could it be from premenopausal symptoms?

So proud of you Deanna. Kiss M S away lots of people will look up to you. A sign of strength to all that suffer with M S Your family are blessed to have a loving daughter like you Keep up the fight a beautiful painting too

so does ms get worser with menopause

apaan tuh

Awesome!

YES! That makes so much sense!

It feels like an electric storm in your legs.

Watching from Oklahoma, USA

I saw a report on ABC news a few months ago where a person who claimed to be from MS Australia claimed to be near curing MS and also claimed that all MS patients had EBV in there body. I am a MS patient who is aware there is no one developing cures, and who does not have EBV in my system, Kind regards, Cameron James

Very nice presentation on multiple sclerosis. Please extend fraternity to ms patients.. ua-cam.com/users/liveY2OIYD_0mPE?feature=share

can the cost of MRI be refunded for a MS Patient?

ALL MS MEDS ARE POISON PROMOTED BY THE MS SOCIETYS.PLEASE WATCH LIVING PROOF WITH GEORGE EBERS AND MATT EMBRY NOW IN CINEMAS .

Such an informative video. I have been suffering from fibromyalgia for over 20 years. During the past year (a year after my husband passed away and after me having a heart attack) I developed a lot of new symptoms which I never had before. I used to walk long distances once or twice a day. Suddenly I couldn’t even walk short distances. My thighs, hips and legs just stiffen up and I can’t walk very far. I have had to purchase a walker to help me walk. About 3 months ago I woke up in the night with severe numbness and tingling in my hands all the way up my arms. The numbness in my arms eased up after about a day, but I have been left with constant numbness and tingling in my hands. I also had disabling fatigue during this time and felt totally “spaced out”. I have also been getting a buzzing sensation in my left upper arm. This is becoming more and more often. During. Vacation last summer I had a very bad reaction to the sun. I have always had difficulty with the heat and sun, but this time I developed a bad rash and it put me in a bad fibromyalgia flare up with painful joints and muscles. I have just seen a neurologist. She thinks my hand numbness and tingling may be carpel tunnel. She is also checking me for lupus and rheumatoid arthritis, and has ordered an MRI of my neck. I seem to have a lot of symptoms of MS, but I think due to my age (76) the doctor isn’t looking at that diagnosis. I know ms usually effects people a lot younger. I have had a lot of symptoms for a lot of years with many very severe flare ups, so I am wondering if I could have had MS years ago and just not had a diagnosis. I don’t always tell my doctor about new symptoms as I always put everything down to fibromyalgia. I have so many symptoms which makes my life a struggle every day with the all over pain, discomfort, fatigue etc., Would you have any comments on my symptoms and anything you would suggest I discuss with my neurologist. Thank you so much for this great video, and for any advice you could give me. I greatly appreciate it. Pam from Canada❤️🇨🇦

Many don’t believe that Parkinson Disease can be reverse treated and cured, all they believe is that there is no cure but I am glad letting you all know that it is all wrong because my friends Mom that has being sick with Parkinson Disease for years just got her Parkinson Disease reversed and cured with a herbal supplements from DR MADIDA on UA-cam.

Still very surprises how all my symptoms of Parkinson’s disease just went aware after undergoing *DR MADIDA* treatment and I am very much happy because I don’t long have experience PD symptoms anymore and strong convinced that I don't have this disease like 9 months now, even my neurologist was thrilled to see me cured with Dr Madida herbs//

Still very surprises how all my symptoms of Parkinson’s disease just went aware after undergoing *DR MADIDA* treatment and I am very much happy because I don’t long have experience PD symptoms anymore and strong convinced that I don't have this disease like 9 months now, even my neurologist was thrilled to see me cured with Dr Madida herbs...

I was diagnosed 3 weeks ago and this topic was certainly at the top of my list of worries on having such a condition. Thank you so much for sharing this is totally a informative pamphlet for partners. 🙏🙏

Can anyone tell me the job title of the person who CAN provide advocacy? Thanks :)

Beautiful!

My first flare was after Covid 19 infection... I have also seen that many people (30-50%) have flare ups after infections (correlating with winter months / spring being flu months + the months where MS patients are most likely to have a flare up). If we consider that spring / winter are two events where MS patients may also get sick this has a very very high impact on ARR just from looking at these basic facts (where ARR on average is about 1.5-2.5). An infection like C19 may weaken the immune system and allow EBV to replicate more - since EBV can hide out in the CNS perhaps the immune system that is already in "attack mode" goes after places where EBV is hiding... including CNS.

So helpful 😊

Thanks for this valuable information. I’m on Mavenclad, if it fails l’ll pursue HSCT.

You explained my symptoms. Except i have not experienced the ms hug. Nerve pain in my feet is tortue 🤔 I always say to myself when will IT END.

Congrats Bek!

I have secondary progressive thank you

I'm trying to wrap my head around some scenarios in a SIL NDIS participant that are allocated funding for irregular supports what would these irregular supports be? to be able to claim for them. Thanks in advance.

Fantastic, fantastic, fantastic - thank you so much for the wealth of information provided!!!

🙏

Excelente Laura, gracias 🌻

Congratulations Laura!