If you’d like to be interviewed and share your story, please email me at info@liss-ms.com!
March 17th 2020, the week the world was shut down due to the pandemic. It was shocking ontop of what was already going on in the world. I didn’t know what multiple sclerosis was and even struggled to pronounce it. I asked my physician if I could just call it “Multiple S.” She then explained to me that yes! People call it MS. I went home and the second I saw my husband I broke down sobbing. It took me almost a year after that to accept my diagnosis. A lot of “why me?” A lot of anger, sadness, depression. Currently, finally getting a handle on the acceptance if the rest of my life.
Daily management of my disease. I have learned a lot, a whole lot! Researched more than enough, at times obsessed with research. It is hard to make the right choices, but in the end its better to be in the “know.”
I am not currently taking medications, but am starting Tysabri June 2nd after more than a year if managing naturopathically.
Fatigue!!!!!! Its definitely the biggest struggle I have. Anxiety and depression have a big part in the fatigue as well, but I am getting better.
Absolutely. Best Bet Diet by MS hope has helped so much to know what to put in my body that won’t hurt me and cause symptoms.
Yes, I have. Positive outlook is the the most important thing to do. Exercise, such as walking really helps. Prayer and meditation are also important. Knowing that your diagnosis isn’t the end of the road and just learning to manage it will be the best thing to know.
All of my family and friends let me process and do what I have felt best for my own life. My parents help me a lot with buying any supplements I need and my husband supports me with any crazy expensive food choices I need. My sweet husband also emotionally supports me so much! My children have learned what mom can and cannot do and have adapted to it. My daughter has caught on so much of my dietary restrictions and makes me special treats that I can eat 🙂
Being selfish, which as a mom that is the most difficult thing to do. Rest when I need rest, say no when i need to say no and to give myself a break when I need a break. It is impossible to keep up, so accepting that you can’t most of the time is impactful.
Breathe and take your time to not jump into decisions. Don’t be pushed, your body is your body.
I’M ALISSA!
I help women who have also been diagnosed with Multiple Sclerosis make specific and personalized diet, lifestyle & subconscious changes so that they can begin to heal their body, reduce disease symptoms, and return to a life they love.hey there,
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