Hello Sara, your sense of frustration is palpable but you need to remember that you are doing amazing with the cruel hand MS has dealt you!! ❤ The rubble of what once were dreams that you may feel yourself stumbling through is where your courage and strength shines the most Sara!! The nature of the beast is that yesterday you could have been able to do quite a few activities but today you may find ourselves sinking in what feels like quicksand. It doesn't take much for MS to sap the strength out of us and that is something we have all to acknowledge and work around with time management. It's by no means a sign of weakness to rest rather it shows that you are taking control of your body. Please don't be harsh on yourself and feel that you are burdening those closest and dearest to you.. you have family and friends who love you dearly and will always be by your side. They see beyond those tears of frustration and see a beautiful soul who lights up this world!! Never forget how far you have come and never forget that you will always triumph over adversity.. Take care of yourself Sara ❤

Thank you for vlogging. It's not easy, but you are so brave to vocalize what many people are feeling, including me, and I have Epilepsy. Most days are really tough.

I'm glad you have a plan for the Keppra.

Thank you for making this video.

You're human. I was just diagnosed 4 months ago, at 63 y.o.!! My attitude this morning was terrible. Just tired of being tired. I'm having a hard time dealing with people, in general. Do you mind if I ask what type of work you do? Thank you for sharing.

Thank you for being real and candid about your condition ❤️🙌

It really sucks sometimes and you should absolutely not feel guilty for having a bad morning or complaining. We are here for you. We know how hard it can be sometimes. And I’m sorry for everything you have had to go through. Sending you all the love and strength. ❤️

We all have some hard days. I walked today with my husband for 15 minutes! That is the most I have walked in years. My foot swells due to an injury and the other has foot drop. I am sure I am a sight as I struggle. But it feels good to keep at this. I just started walking again this month. Keep at it and let the people stare. Eventually they will be used to seeing your apparatus or whatever helps you keep moving.😊Today I hurt. No walking outside. It is a bit too warm for my taste, but that is July.

If I may ask, we’re you taking seizure medication for seizures or for pain management? I’m on two such medications for tremor control and these meds can leave you feeling like your unsteady and not connected with your body. I don’t like that drugged feeling since I have balance issues as well.

Do you think some of your fatigue/sleepiness throughout the day is actually from side effects of the seizure meds you're taking in addition to your MS fatigue/symptoms? I was on seizure meds for a period of time in my life and it made me feel quite sleepy/foggy.