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I'm sure a few of you have now heard this name. Has she invited you to be a friend, whilst mentioning you in an update suggesting love? I've got my eye on her and I'm watching her activities....... You have been warned. :evil:

Hi! I’m I’m Lindah from Sweden. I’m new here so haven’t really figured out what this is all about.

Life & Times of an MS Sufferer….. By Roger Deuxmont · March 31, 2019 Life & Times of an MS Sufferer….. These pages are dedicated to the following people, my father Leslie 1911-1980, my father was an indirect casualty of the smoking lobby, succumbing to the effects of lung cancer at the ag...

Hi everyone my name is rick f. I've had ms rm since 2014. My neourologist is highly qualified at Lima Linda ca. Usa. I've done ok for the most part. On my 2nd ms med tecfedera 2. Years now. Had steroid treatment 2 years Ago for eye vision fine. My left hand. Been numb since I was diagnosed 3.5 yrs...

Hi I'm Linda McIntyre. I'm newly diagnosed in March and would like to know if there's any one on here from miramichi.

Hello, my name is Linda and I'm new to this forum, so please excuse me if I don't work it right. I have mild MS and am on a fairly mild 5000IU of Vitamin D daily. Also trying to do yoga, but it gets harder to balance each time I try. Then someone suggested to do laser therapy (course he has a vest...

Hi, I am confused whether or not my symptoms are of MS or Parkinsons Disease. My Neurologiest is not being helpful. He sent me to every medical profession the ends in a "ist" for months. Im getting tired of his avoidance, I would like to compare similarities with one that had/has the same. If you s...

My friend suggesting me to use various kind of Amway nutrilite products. Is it useful for MS patients, If yes, I can anyone suggest me wa products have to use. #Linda how are you ¿ I don't know waz happening in my life & to where it leads too. Many times I getting thought like without des...

A BACKGROUND TO THE MULTIPLE SCLEROSIS (MS) THERAPY CENTRES OF THE UK AND THE REPUBLIC OF IRELAND Christopher Fox-Walker BA(Hons) There are 65 hyperbaric facilities in the British Isles owned and operated by patients to provide treatment for multiple sclerosis. There a...

I received a Friendship request about 1 1/2hrs ago, from someone with a name that runs in my Family, but on accepting that request, I then received an e-mail with very dubious wording. I have now deleted that Friendship, as well as the email. The friendship request was for a John Miller, but the e-m...

i only share with you the only thing i can do since i was diagnosed to depict the shock & the happiness i live in. by the day tomorrow i was diagnosed with MS. *open this in a code writter app

Happy Friday! I’m new to this space. I’m currently in the process of ruling out what could be going on with me. This post will be a bit long but figured this is a safe space to get it all out. Late Jan 2021 was when I experienced some of my first symptoms. My left upper lip had some numbness. ...

I just came across this article: https://hbr.org/2020/03/that-discomfort-youre-feeling-is-grief Written in the context of the covid-19 outbreak, but does this already sound familiar to anyone else? My synopsis: - Acceptance is where the power lies and where we find control. - Find balance in the ...

After years of seeing reports of no genetic markers found or genetic ties it sounds like this is being looked into. I can't think of any of my relatives with MS but in this group there are constant references to a grandpa that had it or cousins, etc. For a disease that is relatively rare it seem lik...

Hi Guys Long time since I have been on here 3 yrs at least. Just want some advice re tight throat muscles saw my ms nurse last week at my 6 month review she is referring me to speech and language therapist what would I expect from this appointment also do they put you on meds I thought it was due t...

Hi everyone. I have benign MS. I am cycling from London to Brighton on Sunday to raise money for the MS Society. Please see my story below. If you are able to donate a penny or two that would be super. Thank you everyone 😚 much appreciated x https://www.justgiving.com/fundraising/lindsey-pharoah

Hi. Had a Cervical MRI scan. Seeing consultant on 15th. Does any one know what posterior linear suggestive signs of myelopathy at high signal T2. This does not appear to be related to MS as my LP was clear or is it????????. I thought LP would be positive if it was a spinal cord lesion. Any guys know...

Hi please does anybody know what a posterior linear lesion myelopathy is on cervical spine c2 c3. New lesion for me could it be MS developing on my spinal cord. Thanks Guys. X

Anyone experience Tinnitus saw GP about something else ask her about it and she said nothing can be done i.e. treatment if you have had how was it treated. Lina

A team of international researchers from Queen Margaret University Edinburgh and King's College London have been looking at treatments for fatigue in MS, both with exercise and with behaviour, to try to find out which treatments are most effective. - This free session will tell you about what the...