I need a little help. I have a friend newly diagnosed with MS. She is going to the neurologist for the first time next week. It has been a long time since I was diagnosed so I want to be sure to give her the best advice. She has asked what are the questions she should ask of her neurologist. So, I am asking for your input to be sure I don’t miss anything. Thanks.
Help for getting most out of Dr visit. - My MSAA Community
Help for getting most out of Dr visit.
What type of ms has she? What treatment do they recommend? Can she have OT and PT? Get her to write the questions she has on paper and take it with her, that way she won’t forget. Blessings Jimeka 🦋
Perhaps it will be good to ask what she can do about symptoms.
Maybe take someone with her. Or ask if she can tape the conversation.
Hi. My neurologist really appreciated that I chronicled my symptoms, whether MS related or not. You will want to discuss what type of MS you are dealing with. When looking at dis-ease modifying therapy, feel free to discuss your concerns about side effects, and above all - take notes and be kind. Best of luck!
I recommend that she start a daily diary of how she is feeling, what activities she had during the day, what she ate and any symptoms whether she thinks they are MS-related or not. The more information the Dr has the better he/she can recommend treatments. I wish her the best!