“I saw Lyndsay's canes and fell in love with them. If I need to have a mobility aid, I might as well have a cool one. Lyndsay and I became friends and we decided to create one together that benefits the community.”
What would you say to MS if it stood next to you now?
Would you throw your arms around it and say thank you for all the challenges you have presented me?
Would you scream in frustration and ask it why me, why now?
Or would you show it the door and say FUMS?
There is no right answer.
Your answer is right.
There is no right way to live with MS.
The way you live is right.
Just know you are not alone.
The entire chronic illness community is behind you, empathizing and willing you on.