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Multiple Sclerosis MRI - New and old active lesions

Multiple Sclerosis MRI's and check ups usually happen regularly and I believe they are imperative when you've suffered a recent Multiple Sclerosis relapse. As I had a quite debilitating Multiple Sclerosis relapse, which affected a new part of my body, my neurologist wanted to have a new MRI of my brain, neck and spine. I had an MRI scan with and without contrast. A scan with contrast allows any active Multiple Sclerosis lesions to be identified. It's really simple, they either put the dye into your body through a cannula before the scan or during the scan. The dye isn't harmful however, It is recommended you drink plenty of water afterwards to flush it out of your system. Unfortunately my scan showed I had new Multiple Sclerosis lesions, that were active, in my cervical spine. My old lesions were all active too. My neurologist called me to discuss the MRI results and said she expected what she saw on my scan due to my current health status. I have a form of Multiple Sclerosis called, Relapsing Remitting Multiple Sclerosis. After my scan, the form of my Multiple Sclerosis didn't change however, it was moved into the highly active category. Due to this, my neurologist wanted me to, as soon as possible, commence a new and stronger form of medication. As always, I asked my neurologist what my prognosis would be if I didn't take medication, she said she couldn't say. I asked what my prognosis would be with medication, she said she couldn't say. This is the difficulty with Multiple Sclerosis, not one person can say or know what is going to happen or when, with or without medication. You can only go by statistics. I have had two types of Multiple Sclerosis medication so far. My body unfortunately rejected the one type and I didn't feel well on the other type. so, I suppose it's decision time for me. I have been given three different medication options to choose from. I've done a little bit of research but will need to do more before I can make a final choice. If you or someone you are supporting are trying to make Multiple Sclerosis medication choices then remember, your MS team and your neurologist can spend time with you discussing your questions. Other places to find help regarding Multiple Sclerosis medication choices: MS Trust The MS Trust has a really great resources section here: https://mstrust.org.uk/resources MS Society The MS Society has a searchable information publications section here: https://www.mssociety.org.uk/care-and... As always, if you have any questions please get in touch. Until next time, stay healthy, see you soon x