Hey beauties!
So this past friday 7/23 was my 25th birthday! I must say I am truly blessed to have made it this far in life. I am so grateful for my boyfriend,parents, best friends and host of coworkers and family members. My coworkers gave me a surprise 25th bday luncheon and it really made me cry tears of joy. With everything going on this year I just had no idea they were planning it for weeks!!!
My boyfriend took me to a great dinner and we even danced a little. I had alot of fun. I received many gifts and birthday wishes. Hmmm never knew 25 could taste so good! ;D
Wednesday, July 28, 2010
Friday, July 16, 2010
When it Rains it pours...but the Rainbow follows ♥
Hey beauties!
that is what I caught myself saying over and over..When it rains it pours. Sometimes the pain and numbness is out of control! Crying, huffing and puffing...but then somewhat of peace breaks through. The images that collide in my head such as the smile of my boyfriend, my wonderful hard working parents and brother, my best and close friends hugs, the laughter of their children along with my Goddaughter. That's when the rainbow peeks through after the rain.
MS affects not only the person who is dx with it but also all of the loved ones. I try to remember, as hard as this may be for me, I know it is rough on my loved ones as well. God is so good though because we are such a great support system. I know God has a big plan for us, and I am hanging in there for the journey!
Many blessings beauties
that is what I caught myself saying over and over..When it rains it pours. Sometimes the pain and numbness is out of control! Crying, huffing and puffing...but then somewhat of peace breaks through. The images that collide in my head such as the smile of my boyfriend, my wonderful hard working parents and brother, my best and close friends hugs, the laughter of their children along with my Goddaughter. That's when the rainbow peeks through after the rain.
MS affects not only the person who is dx with it but also all of the loved ones. I try to remember, as hard as this may be for me, I know it is rough on my loved ones as well. God is so good though because we are such a great support system. I know God has a big plan for us, and I am hanging in there for the journey!
Many blessings beauties
Sunday, July 11, 2010
1st day of Avonex
Yesterday I started my first day of Avonex. The nurse, Veronica, came over to train my parents, one of my best friends, my darling boyfriend and myself how to inject the drug. It went pretty well and having my support group really helped me hold it together. I feel like God knew what he was doing when he made us. I'm really blessed to have wonderful parents,an amazing boyfriend and great best friends.
I say all was well for most of that evening, my legs were bothering me but not unbearable at least until I got home after dinner....
My darling boyfriend brought me home, I wanted to take a shower so that I could relax. Now if anyone knows me knows I love hot steamy showers however with being diagnosed, I can no longer do the extreme hot environments because it can cause an episode to happen. So that means no HOT showers, no saunas and I have to even becareful when I'm outside now during the summer. So as I took my shower it was on warm, I was doing ok my legs were still a lil wobbly but I thought I was fine. Until I was drying myself off and my legs gave out on me :( .
I cried, my mom heard me and said what happened and I told her that my legs gave out on me. And she got sad but what else are you left to do? I got myself together and got UP. Yes it hurt my knees when I fell, Yes once again I felt embarrassed however I cant just stay there.
I was told that one side effect of the disease modifying drugs are depression. Personally, I feel it is real easy for a professional to slap many labels to people who have a condition. I feel like anytime you have change in your element or you do not operate like your "usual" self, anyone could be sadden by that. I want to be a fighter against the disease. Yes I will get knocked down, mentally and physically but I'm refusing to stay down.
I pray that God continues to give me strength. I am so blessed and happy by His Grace in which that has gotten me this far. I am once again mentioned blessed for my loved ones, they give me the inspiration to proceed to carry on. I loved them more than they will ever know. Until next time :D
Later beauties
Nikki
I say all was well for most of that evening, my legs were bothering me but not unbearable at least until I got home after dinner....
My darling boyfriend brought me home, I wanted to take a shower so that I could relax. Now if anyone knows me knows I love hot steamy showers however with being diagnosed, I can no longer do the extreme hot environments because it can cause an episode to happen. So that means no HOT showers, no saunas and I have to even becareful when I'm outside now during the summer. So as I took my shower it was on warm, I was doing ok my legs were still a lil wobbly but I thought I was fine. Until I was drying myself off and my legs gave out on me :( .
I cried, my mom heard me and said what happened and I told her that my legs gave out on me. And she got sad but what else are you left to do? I got myself together and got UP. Yes it hurt my knees when I fell, Yes once again I felt embarrassed however I cant just stay there.
I was told that one side effect of the disease modifying drugs are depression. Personally, I feel it is real easy for a professional to slap many labels to people who have a condition. I feel like anytime you have change in your element or you do not operate like your "usual" self, anyone could be sadden by that. I want to be a fighter against the disease. Yes I will get knocked down, mentally and physically but I'm refusing to stay down.
I pray that God continues to give me strength. I am so blessed and happy by His Grace in which that has gotten me this far. I am once again mentioned blessed for my loved ones, they give me the inspiration to proceed to carry on. I loved them more than they will ever know. Until next time :D
Later beauties
Nikki
Friday, July 9, 2010
Falling..
So I am becoming more and more clumsy these days. I mean I do laugh at myself when I trip over nothing and I'm around my comfort zone until today...
Today I parked my car in front of my house and I was moving it so my father could park his car there, then all of sudden I landed on the ground and my left hand caught me (if that makes sense). My neighbor came over and helped me and kept asking if I were ok and I said yes. I was so embarrassed, as soon as I got in the house I cried.
I know its like Nikki its not a big deal people trip all the time. the part .that gets to me most is I cant remember it. like I cant remember how I fell or why, I honestly thought I reached the last step...but the good news is I'm ok and I will continue to keep track of these things.
Today I parked my car in front of my house and I was moving it so my father could park his car there, then all of sudden I landed on the ground and my left hand caught me (if that makes sense). My neighbor came over and helped me and kept asking if I were ok and I said yes. I was so embarrassed, as soon as I got in the house I cried.
I know its like Nikki its not a big deal people trip all the time. the part .that gets to me most is I cant remember it. like I cant remember how I fell or why, I honestly thought I reached the last step...but the good news is I'm ok and I will continue to keep track of these things.
Saturday, July 3, 2010
My meds are here!
hey beauties!
I am so happy my meds are here. People do not realize the power of prayer. I work a job 40hrs per week with no benefits and I was stressed out worrying how am I going to afford this medication? God is good because the company has an Access program which is for people with MS that are uninsured..I was approved! :D
So the next thing to happen is for me to receive training from the nurse on how to use the syringe for the injections. I have to do them once a week..yikes!!! but my parents, bf and bff will be there for support and to train with me :D
Along with me starting the meds, I have to change my eating habits too. I am going to cut back on the red meats and grains :( I love me some hamburgers (homemade not mcdonalds etc) and I love pasta!! Even though I eat whole wheat pasta and bread I still want to cut back my intake. I believe I will see a difference in how I look and feel :D
With the information given to me about Avonex I received a black journal book, in which I will track how each day is going with the meds but I'm also going to track how my eating habits are too. I read many place where they said that certain foods are triggers for excaberations.
I'll keep a post on any new updates..Thanks to those who follow this blog I appreciate it ♥
I am so happy my meds are here. People do not realize the power of prayer. I work a job 40hrs per week with no benefits and I was stressed out worrying how am I going to afford this medication? God is good because the company has an Access program which is for people with MS that are uninsured..I was approved! :D
So the next thing to happen is for me to receive training from the nurse on how to use the syringe for the injections. I have to do them once a week..yikes!!! but my parents, bf and bff will be there for support and to train with me :D
Along with me starting the meds, I have to change my eating habits too. I am going to cut back on the red meats and grains :( I love me some hamburgers (homemade not mcdonalds etc) and I love pasta!! Even though I eat whole wheat pasta and bread I still want to cut back my intake. I believe I will see a difference in how I look and feel :D
With the information given to me about Avonex I received a black journal book, in which I will track how each day is going with the meds but I'm also going to track how my eating habits are too. I read many place where they said that certain foods are triggers for excaberations.
I'll keep a post on any new updates..Thanks to those who follow this blog I appreciate it ♥
Wednesday, June 30, 2010
Biogen Idec
So this week my new neurologist referred me to Biogen Idec (Avonex manufacturers). I received a phone call and plenty of useful information. Once I feel out the consent forms and send my w-2's for financial assistance I will began treatment. I am very nervous about this but I have a wonderful support system and I know I will be fine :D
Yesterday I hung out with of my girlies whom as well has MS. we walked along the park and she gave me alot of insight from her own personal experience with Avonex and pointers for when I start treatment. I have to say though after the walk...My legs were beginning to get weak on me and I was just ooo no. However, I kept pushing, and with the thought of seeing my wonderful boyfriend I gathered the strength to drive home.
Last night I cried, the pain. What was even worst was bad thoughts of what if the meds don't work or this how things will be for the rest of my life? Instead of driving myself crazy I prayed and continuously ask God for strength. Once I relaxed and took deep breaths, I drifted off to dream world :D.
This morning was a good day. I had a few minor off sets but I managed :)
Yesterday I hung out with of my girlies whom as well has MS. we walked along the park and she gave me alot of insight from her own personal experience with Avonex and pointers for when I start treatment. I have to say though after the walk...My legs were beginning to get weak on me and I was just ooo no. However, I kept pushing, and with the thought of seeing my wonderful boyfriend I gathered the strength to drive home.
Last night I cried, the pain. What was even worst was bad thoughts of what if the meds don't work or this how things will be for the rest of my life? Instead of driving myself crazy I prayed and continuously ask God for strength. Once I relaxed and took deep breaths, I drifted off to dream world :D.
This morning was a good day. I had a few minor off sets but I managed :)
Sunday, June 27, 2010
Long Island girl too slow for Busy Brooklyn Job
Hey beauties!
This blog is going to be documenting my story of choosing happiness and living life even though I'm being diagnosed for Multiple Sclerosis. For those who do not know what MS is I am pasting the description from the National MS Society website :
Multiple sclerosis (or MS) is a chronic, often disabling disease that attacks the central nervous system (CNS), which is made up of the brain, spinal cord, and optic nerves. Symptoms may be mild, such as numbness in the limbs, or severe, such as paralysis or loss of vision. See nationalmssociety.org for more info :D
Ok so in April 2009 I was working in dtown brooklyn as a caseworker for a foster care unit(started march). I was under alot of stress and please believe ask any caseworker/social worker about burn-outs and being emotionally drained, its so serious. As I got used to my new schedule for work, I noticed that my legs would get weak and numb on me. I just thought maybe the city atmosphere was too hectic for me especially since I'm from long island.
These symptoms continued until the saturday before mother's day, My boyfriend and I went to the movies. I felt so off balanced and my legs were giving me troubles. It got so bad that when the movie was over I need assistance from him to walk. My boyfriend then took me to the emergency room and they said it was possibly vertigo. I thought hmmm that makes sense and the er doc did recommend me seeing a neurologist but I never went. However I ended up leaving the caseworker job and returned to my old job.
My legs continued to bother me and I would just brush it off as "o my vertigo is acting up" and I would take the mecclazine (sp?) to sleep it off. This cycle of my every day experience continued through the summer, fall and winter and early spring but then another episode happened. At the end of March I was watching tv and I went to reach for my cup of juice when I notice I never grasped the cup I thought it was because I was grabbing in the wrong direction not true. I was holding the cup the whole time and I couldnt feel it. My hand and arm was weak and numb which scared the heck out of me. So a week later one of my co-workers gave me info about her neurologist and I went to see her. I explained everything that happened to me and I also explained that I didn't have insurance. A radiology office Zwanger-Pesiri here in Long Island have a program they call "give back sundays" which the radiologist give their services at no cost. I was able to get 4 mri's done.
I say about a week later the neurologist called me and told me that they found 9 lesions on my brain. A week later I saw her in the office and she told me that it was MS. I kinda knew because I had been researching on webmd and alot of the issues I was experiencing were associated with MS and once I found out about the lesions I learned that the lesions are apart of it. My mother was there along with me and she was very strong. The hardest part was when we got home telling my Daddy and my boyfriend. My best friends were all devastated and upset and angry. I told them I need them to be strong because I too will break.
So since finding out in April I notice the difference in my body during the hot weather. I'm experiencing pain. I'm experiencing issues with other body parts such as my fingers,arms, and toes. I've also learned that this twitch in my eye that I had for years is associated with ms, its called tremors :( and I am learning how important it is to keep my body cool and to keep the stress level down.
Well that is what is going on in a nut shell. I have another blog svrbrownsuga.blogspot.com where I also mentioned the symptoms and my daily experiences but I want this chapter of life to have it's own attention.
*Smile* Nikki
This blog is going to be documenting my story of choosing happiness and living life even though I'm being diagnosed for Multiple Sclerosis. For those who do not know what MS is I am pasting the description from the National MS Society website :
Multiple sclerosis (or MS) is a chronic, often disabling disease that attacks the central nervous system (CNS), which is made up of the brain, spinal cord, and optic nerves. Symptoms may be mild, such as numbness in the limbs, or severe, such as paralysis or loss of vision. See nationalmssociety.org for more info :D
Ok so in April 2009 I was working in dtown brooklyn as a caseworker for a foster care unit(started march). I was under alot of stress and please believe ask any caseworker/social worker about burn-outs and being emotionally drained, its so serious. As I got used to my new schedule for work, I noticed that my legs would get weak and numb on me. I just thought maybe the city atmosphere was too hectic for me especially since I'm from long island.
These symptoms continued until the saturday before mother's day, My boyfriend and I went to the movies. I felt so off balanced and my legs were giving me troubles. It got so bad that when the movie was over I need assistance from him to walk. My boyfriend then took me to the emergency room and they said it was possibly vertigo. I thought hmmm that makes sense and the er doc did recommend me seeing a neurologist but I never went. However I ended up leaving the caseworker job and returned to my old job.
My legs continued to bother me and I would just brush it off as "o my vertigo is acting up" and I would take the mecclazine (sp?) to sleep it off. This cycle of my every day experience continued through the summer, fall and winter and early spring but then another episode happened. At the end of March I was watching tv and I went to reach for my cup of juice when I notice I never grasped the cup I thought it was because I was grabbing in the wrong direction not true. I was holding the cup the whole time and I couldnt feel it. My hand and arm was weak and numb which scared the heck out of me. So a week later one of my co-workers gave me info about her neurologist and I went to see her. I explained everything that happened to me and I also explained that I didn't have insurance. A radiology office Zwanger-Pesiri here in Long Island have a program they call "give back sundays" which the radiologist give their services at no cost. I was able to get 4 mri's done.
I say about a week later the neurologist called me and told me that they found 9 lesions on my brain. A week later I saw her in the office and she told me that it was MS. I kinda knew because I had been researching on webmd and alot of the issues I was experiencing were associated with MS and once I found out about the lesions I learned that the lesions are apart of it. My mother was there along with me and she was very strong. The hardest part was when we got home telling my Daddy and my boyfriend. My best friends were all devastated and upset and angry. I told them I need them to be strong because I too will break.
So since finding out in April I notice the difference in my body during the hot weather. I'm experiencing pain. I'm experiencing issues with other body parts such as my fingers,arms, and toes. I've also learned that this twitch in my eye that I had for years is associated with ms, its called tremors :( and I am learning how important it is to keep my body cool and to keep the stress level down.
Well that is what is going on in a nut shell. I have another blog svrbrownsuga.blogspot.com where I also mentioned the symptoms and my daily experiences but I want this chapter of life to have it's own attention.
*Smile* Nikki
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