Looking for
something specific?

Hi. My name is Cara & I have had MS for 15 years. I started a company, The SwitchVR, 3 years ago. Our purpose is to develop holistic therapeutics (i.e. meditation, mindfulness, Qigong) using technology so that we can offer complementary practices for MS patients, like myself. Our first product i...

Sounds promising. Mechanisms Identified to Restore Myelin Sheaths After Injury or in Multiple Sclerosis https://neurosciencenews.com/myelin-restoration-16896/

Kanavance CBD Pharmaceutical grade fish oil is oil that has been purified through a process called molecular distillation. It is the only grade fish oil approved for humans. The best fish sources of Omega 3 fatty acids include herring, mackerel, and salmon. Kanavance CBD The Hoki fish from New Zeala...

Hey Peeps. Spoke to the consultant yesterday, my yearly follow-up which went ok apart from mentioning about armpit, arm and neck and shoulder pain. I was referred to the breast clinic in March which they checked me over and just said lumps were normal and having no history in the family was a good...

Hi All, I am new to this site and wanted to introduce myself. I was unofficially diagnosed with MS whilst living in the US but due to limited understanding and MRI facilities in the UK, not officially diagnosed until 2008. Currently medically retired and enjoying life. I have spent the lockdown peri...

Well after a few weeks of rest at home I'm now back to work, and so thankfully to be. My son's would like to see me take off more time, but as I have told them I have always liked working and I will continue to for as many more years as I'm able. I'm a stubborn women, I guess but I will not give in...

www.link.com test

I am in the process of applying for PIP and have completed the online mock PIP tests on the Benefits And Work website. All the questions seem to be geared towards assessing mental illness and physical disability though. Non of them seem to assess fatigue, which is my main symptom (especially on bad ...

I know there is lots here about optic neuritis, but I wanted to ask if anyone has had their vision recovered but been left with discomfort ever since. I had ON a year ago and lost partial vision in the eye but it returned within 2 months. However now a year on I Continue to get intermittent but dail...

Afternoon. Sorry it’s a long one. I’ve had the best couple of months, I’ve been able to go out and about. However last night just before bed, I started to feel funny ( massive pins and needles/pains in my legs and one arm) which can be normal once I’ve got into get and relaxed. However this wasn’t ...