Tag: ms

The weather

As a child, I never quite understood how older people could tell it was going to rain or when they said “It’s cold, I can feel it in my bones”. It’s funny how life happens because now I say similar things!

Since being diagnosed with MS, my body lets me know if the humidity is high, if it will rain, and if the temperature is very cold. I experience leg weakness during this time, numbness in toes and sometimes very painful nerve pain. As I type this post, my left big toe is curing numb and I’m having nerve pain in both legs. It really sucks.

However, the show has to still go on. On days like this, I still have to be wifey, mommy and assistant supervisor at work. I pray to God for strength, as tears may flow down my cheeks and slowly get it together. I know there are others who experience this and more. There are other warriors with physical ailments and mental issues that can be thrown off due to the weather.

When it rains, it pours. I wish, I could cut back some of the storms, but unfortunately that can’t happen and that’s Life. How we choose to manage IS up to us.

We can let the weather take over us and our spirit or we can dance in the rain and view the rainbow that follows.

Thanks for reading,

Nicole Cherise ♥️

Whatever don’t……

“Whatever don’t kill me, Gets me through the day”

All praises to the Lord for providing me the strength and guidance to Keep Going even when my body is attacking itself.

My hope is that anyone who is going through the storms in their life, please remember you are NOT walking alone. Sometimes the weight of physical and mental health leaves you to feel as if your too weak, no my friends you Won’t FALL!

Nicole Cherise ♥️

Just Keep Swimming


Sometimes, the tears overflow from being overwhelmed with pain and numbness caused by MS. Feeling of dizziness, dragging my left leg around, has become the new “norm”. 

No matter how much I cry, I have to keep moving. Just like in the movie, “Finding Dory” we have to “just keep swimming, just keep swimming”. 

We are strong friends. We will claim victory. We don’t have to give up or give in. We got this!! Keep Going!

Thanks for reading!

Nicole Cherise 

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Fight on MS Warrior

Hi great people!

Today was the Long Island MS Walk. I’ve walked every year since I was diagnosed in 2010. However, lately, I was in a rut about going. I wasn’t feeling my best physically or mentally. It wasn’t until 8 am this morning when I said, “Ok I’m going”. My team came with me and we had a good time. 


I met a very nice woman named, Margaret Murphy who works at the National MS Society Long Island Chapter. I told her that I plan to be more involved with MS events in the future. I also did my annual pic with  my dear friend Erin who inspires me so much! 


So it turned out to be great after all and I’m happy I went! I’m blessed to have my supporters from near and far. Those who have helped me spiritually, those gave those pep talks and donated to the National MS society! Because of you, someone can get assistance with wheel chairs, walkers, coverage for treatment and the list goes on. On behalf of MS Warriors, THANK YOU! 

I hope everyone is having a good weekend so far! 😊

Nicole Cherise ❤️

Confession

Hi great people!

As a person who battles a chronic illness (Multiple Sclerosis), I am doing my best to remain strong. I do KNOW that my strength comes from the Lord 💪🏾 therefore, giving up can never an option.

I would be a liar if I said I wasn’t scared. I don’t let these feelings consume me everyday because I’m trying to enjoy every moment of life. To help me with this is that I look to my loved ones as my “why” and Purpose. 

What about my other warriors out there? Those who battle illness, has this been you? 

Thanks for reading friends!

Nicole Cherise ❤