How many can say that this has happened to their device chargers? YUP, TOO MANY! How many can say that they KNOW what this feels like? 🙋🏾♀️ I can, along with other MS Warriors. This is exactly what happens to the Myelin (covering of the nerves) throughout our Central Nervous system. For myself, the damage leaves me with mobility issues, numbness, nerve pain (inflammatory disease as well), cognitive issues and of course Fatigue. Some other warriors have eye issues called optic neuritis and their vision is blurred, doubled or gone. We don’t ask for sympathy or pity. We ask for understanding, support and for people be educated. I’m so thankful for my loved ones who have supported me during this journey! Even though I get tired, frustrated and sad, please know… I’m NO QUITTER. Ok?!!! Your girl still has work to do! Love you all!! 💪🏾💪🏾💪🏾🧡🧡🧡💪🏾💪🏾💪🏾
The past few days have been so tough friends. From falls, wobbly legs, nerve pain in my arms and legs, your pal is TIRED! However, I’m still Showing up and Not giving up! I’m here for you if you have these moments. Rather it’s Physical, Mental or even Spiritual, I’m here for you 🧡 Stay blessed, Be Well 💫
Hi all!! Today is my 8th wedding anniversary. I’m extremely blessed and thankful to continue this journey with my bestfriend 😁♥️😁.
When I was first diagnosed with MS (4/13/2010) and learned about the debilitating disease, we were 24 years old. In my head, I thought the chance of having a fulfilled relationship was no more. Who would want to marry me when I’m sick? With the progression of the disease, my body would never be the same, who has the patience for that? I was preparing myself to no longer be with my high school sweetheart because I didn’t want to hold him back. As I shared the news it was devastating to us all, a lot of anger, tears, frustration but one thing stuck out. My then boyfriend said “I’m going to take care of you, I got you”. At the end of that year he asked me to marry him (12/25/2010) and we married 8/9/2012.
To all my dear friends and loved ones who battle illnesses, love and support goes a long way. Please don’t give up on the hope that you can have a meaningful relationship or marriage. Don’t let the disease take that away from you. You are worth MORE than these doctor reports. Thanks for reading! Have a great day!
It’s been a while and I thought it would be great to come back on a day that’s so important to me. One this day 10 years ago I was diagnosed with Multiple Sclerosis (MS). It was a day that brought so many emotions but mostly ANSWERS AND CLARITY.
Through this battle, I’ve grown tougher skin, resilience, and a strength that was unknown to me. Wobbly legs, Numbness all over my body, nerve pain, headaches, confusion, memory issues, trigeminal neuralgia, uncontrolled shakes and falling because my legs give out on me; are most of the symptoms that my battle consist of. With this battle, I don’t fight it alone.
My family, friends, church family, and work family and MS Warrior family, have been extremely supportive throughout the journey. Because of them, I’m inspired to have purpose and to NEVER give up. Therefore, I’m so blessed to have a great support system.
Here I am today, ready to give birth at any moment and reflecting on a monumental day in my life. Thank you all for your support, donations to our “Nicole Cherise” team and most importantly prayers. I love you all, thanks for reading!
Last night, I had the honor of attending the National MS Society Long Island Chapter event. It recognized the top fundraisers for the Walk MS 2019. Team Nicole Cherise earned a little over $1700 and we were placed at number 64!!! I’m so thankful to those who have walked with me and supported our team for such a cause that is near and dear to me. Next year will be TEN years diagnosed with MS and I will continue to spread awareness and fight for a cure! God bless you all and let’s get to work for 2020!!!
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.
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!
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!
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!!!