Tag: ms

‘Harry Potter’ author JK Rowling makes $18.8M gift for MS research

— Read on www.usatoday.com/story/entertainment/books/2019/09/12/harry-potter-author-jk-rowling-makes-18-8-million-gift-ms-research/2304194001/

This, is excellent news and means a lot to Us, MS Warriors!!! The more funding, the closer we are to finding a cure!

I can’t to say,” I remember when I had MS”!

Nicole Cherise ♥️

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MSversary-4/13/2010

On today, 9 years ago, I was diagnosed with Multiple Sclerosis. After receiving the news I felt relief. I was experiencing symptoms for a year before getting this news and I was just happy that I wasn’t crazy. The symptoms at that time was numb and weakness on my left side of my left shoulder, arm, fingers, leg, feet and toes. I would fall, and needed assistance to walk. My hands would fall asleep a lot and I battled nerve pain. It all made sense once the neurologist showed me the images of my Brain that at the time had 9 lesions on it. This was all the confirmation I needed.

I’ve learned a lot about myself since the diagnosis. I realized that I am strong, my Faith was tested, I can be too critical of myself, it’s ok to say “No” and I learned the importance of support.

The Long Island MS Walk is May 18th and I’m super excited this year. I will have my family, friends and some friends from work to walk along with me and other MS Warriors.

Thank you to my family and friends for loving me and all of the challenges that may come with me. Thank you to all who have prayed for me. Thank you to those who reach out to see how I’m feeling. Thank you to those who donated to our Walk MS team “Nicole Cherise”. Thank you to those who have reached out to me for support during their own MS diagnosis. Lastly, thank you to my New MS Warrior friends, we are in this journey together and I love the fact that I can chat with others who can Relate.

The Fight Continues 💪🏾💪🏾💪🏾

Nicole Cherise ♥️

Thumbs up for MS Warriors!!!

Hi friends!

Where is the Love for the MS Warriors? Right here!!!

As I’ve written before, March is MS Awareness Month and this week is MS Awareness week. Even with my wobbly legs, I am continuing to Push Through!

MS ribbon earrings

I made a choice to show up strong for my loved ones, go to work even when it hurts, and I’ve modified outfits so that I’m comfortable as an effort to beat the challenges of MS. There are some days that I’m not able to give 100% but trust and believe giving 0% is NOT an option .

To my fellow Warriors and Caregivers, I’m proud of you for Not giving up. The Pain and Depression is real and can effect us but I believe in You! I also believe that we will be Victorious against this horrible disease. Therefore, I will continue to send spiritual and positive energy your way! Thank you all for being supportive to me as well!

Much love to all and Thanks for reading 🧡

Nicole Cherise-MS Warrior since 4/13/2010

Pushing Through

Hi friends, happy Tuesday!

Push through…

That’s something I continue to tell myself during challenging times. It’s not easy battling a difficult disease like MS, but I can’t give in to it. I know many that read my blog, are battling other autoimmune diseases, mental health issues, or spiritual brokenness. I also, know that Caregivers have a challenging task when it comes to watching someone they love suffer. WE ARE NOT ALONE! Together, we can lift one another up because Support goes a long way.

This past week, I had my Tysabri treatment and the days after were rough. I had difficulty walking, it was a task to get dressed, I fell twice and I cried because of the pain and weakness in my legs. Even during this time of despair, I promised myself that I wouldn’t give up and I would PUSH through it all at my own pace. I urge you all to do the same. I went to the gym on Sunday and did my best with what I had for that day (I do the spoon theory in my head lol). The amount of support that was given to me was overwhelming and it truly melted my heart. People re-posted my video and tagged me as Inspiration for them to exercise.

Please continue friends. Don’t give up on yourself or the process. Below is the video that I posted and keep in mind that days prior, I was not able to walk far alone. God is good. Thanks for reading!!!

Nicole Cherise ♥️

Motivational Monday: the Sunrise

Happy Motivational Monday friends!

I know Mondays can come in tough especially when we had a busy weekend and a pending busy work week ahead. I, too, have to really push myself as well but today was different.

I over slept today, had to rush to get my son ready for preschool and as we were waiting for his bus, I saw the sunrise. It was at that moment that I picked him up to view it as well. Now, I know you may be thinking what’s so special about that? It’s special because I haven’t been feeling well.

Ever since the Wednesday before Thanksgiving, my left leg has been on and off weak, I’ve been experiencing nerve pain in the left side of my head and a new recent issue with my ear. I have not been able to HOP out of the bed, I’ve needed walking assistance during the first steps after getting out of the bed. Also, as I held my son watching the beautiful sky, I realized that I haven’t been able to hold him for that length of time the past couple of weeks. Therefore, I immediately thanked God.

As a Multiple Sclerosis (MS) Warrior, I have to be grateful for those moments because the disease is unpredictable. I’ll feel great now then a hour later, it can go down hill again. On today though, I had another chance at Life. Just as the Sunrises, I know many are fighting their lives just to see that and I won’t take that for granted. I’m here for a reason, another opportunity to succeed while the sunrises for my soul. If you’re reading this, you too had another opportunity at the hustle and bustle of life.

Friends, I hope you have a wonderful week, I’m grateful for your support and I’m here to support you as well!

Thanks for reading!

Nicole Cherise ♥️

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 ♥️