Hi Alina, Ryan sends his regards 🙂 I’m sorry about your recent diagnosis. I’m sure it isn’t easy, however, like you said, somewhat relieving. Because now you know and you can start battling something that has a name. Sadly Fibro is still very much misunderstood by both the medical community as well as society, so I know that it’s a struggle. But reach out. Yes, it might be a struggle for your family too, but reach out to them anyway. It’s important not to isolate yourself. I’d be happy to know you’re following my blog and please do keep in touch its a pleasure to hear from all of you. xx Keep safe !

Hi Roxanne, it is in fact the hardest part of MS I think. Even harder than the aches and pains and the physical struggles, is how misunderstood we all are. So we need to try and change that. If we can’t change it by explaining to our loved ones, we can chance it by reaching out to each other. 🙂 Stay safe! Keep in touch. I see you. I understand. xxx

Hi Kylie, I’m so glad you’re telling me this! This is exactly why I wanted to write this blog. Because I was you, and still am. But no we aren’t alone and like me and you, there are many others, so we should reach out to each other! I hope you keep following my blogs. More out soon! 🙂 Keep well xx

Thank you David xx

Remember this though; they try and make you forget because it’s hard for them to accept. It has nothing to do with you but a lot to do with them. So don’t let them get to you. Thank you 🙂 xx