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MultipleSclerosis.net
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At MultipleSclerosis.net we empower patients and caregivers to take control of Multiple Sclerosis by providing a platform to learn, educate, and connect with peers and healthcare professionals.
At MultipleSclerosis.net we empower patients and caregivers to take control of Multiple Sclerosis by providing a platform to learn, educate, and connect with peers and healthcare professionals.

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I can hardly imagine a day where I’m not constantly aware of the time due to my alarms telling me it’s time to eat, time for an appointment, time to do labs, time to something-something-something: https://multiplesclerosis.net/?p=34809
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I’ve learned that if the random thought of the bathroom crosses my mind I should act upon it, even if I don’t physically feel the need to go to the restroom…yet. https://multiplesclerosis.net/?p=14552
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We want and need more than medication and tests to deal with living with a chronic disease. We need compassion and reassurance: https://multiplesclerosis.net/?p=34817
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Most of the time, I walk around and look pretty normal. At least, I do until I don’t, and I’m suddenly on the floor...most folks who don’t know me think I’ve just had too much to drink: https://multiplesclerosis.net/?p=34607
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I had no idea how I would handle being a mom with MS. I was terrified I would be too exhausted and weak to be able to care for my own child. https://multiplesclerosis.net/?p=34748
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How MS patients lost their patience, got mouthy, and the FDA listened: https://multiplesclerosis.net/?p=29078
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With MS, physical symptoms can sometimes be easier to talk about than mental or emotional symptoms, but they are all linked: https://multiplesclerosis.net/?p=33838
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We may need a cane, or a wheelchair, or some other apparatus, but we persist because we have to: https://multiplesclerosis.net/?p=34361
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Vacation is supposed to be about letting go of your everyday stresses and allowing relaxation and a much needed break from the outside world. But, it’s not that easy with MS: https://multiplesclerosis.net/?p=27647
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What do you keep in your MS management kit when leaving the house? https://multiplesclerosis.net/?p=33235
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