Disclaimer: This page may contain affiliate links. We may earn a small commission for purchases made through links in this post, at no extra cost to you.
Name: Jodi Rivera
Location: Spring, Texas
Year Dxed: 2007
How many years with MS: 6 years
Type of MS: Relapsing-Remitting MS
A little about Jodi:
My name is Jodi Rivera and I currently live in Spring, Texas with my husband Randy Rivera and our son Elijah Rivera. I was diagnosed in 2007 and have been dealing with MS now for over 5 years. The type of MS that I currently have is RRMS.
I was a young mother and young wife when I was first diagnosed with MS. It was a scary time in my life because I was having difficulty seeing and my vision was blurred for many weeks. I finally went to my eye doctor who told me that this is something more serious. He told me I needed to immediately go to the emergency room because I could have a brain aneurism. I immediately was rushed to the hospital to begin testing to find out what was going on. I had several MRI, I had a spinal tap, I was pumped up with a lot of steroids and I was given many different meds including strong pain pills to ease the pain. My stay at the hospital was almost 2 weeks only to learn that they did not find MS and they finally released me with a diagnosis of optic neuritis.
I found one of the best neurologist in my area who was sure that I had MS but it just has not surfaced yet. After my spinal tap my blood started leaking out of my spine because they put too big of a hole in my spine. I then suffered tremendous pain from the blood leaking into my body. I was rushed to the hospital again only to undergo another procedure to take my blood, clot it and reinsert my blood at the site of the spinal tap. Finally they stopped the bleeding and I was feeling better.
My neurologist wanted the to do another MRI only 3 months after my hospital stay. He said if we can catch this literally onset you will be in really good shape. I of course agreed and would undergo as many MRI as needed. My results from my very first MRI was finally positive for MS. I am very blessed that I have been able to catch this disease in the early stages and I know that I will live a normal healthy life.
As a strong faithful family we make an effort in raising money for MS. My husband Randy Rivera and our son Elijah Rivera are my GREATEST supporters!!! My husband who has never picked up a road bike in his life, began bike training so he can do the MS 150 in honor of his wife! He has continued to do this year after year and I am so proud of what he is doing not only supporting me but many of other that struggle with MS. My son Elijah is also involved and actually next weekend we all will be walking for MS as a family! I am blessed with an amazing family and friends who support me year after year!
Never give up on your fight, stay positive and don't give up because you can beat MS! I am beating MS everyday and nothing can stop me. Stay strong!!!
Please also remember to stay on your medicines. I am currently taking a daily shot of Copaxone and this has helped keep the disease at bay. Do your research and stay on top of the new findings. We can do this, MS will be a disease of the past!!!!
Use this easy form to create pages in your room. Share your thoughts and advice about MS. You can add poems or stories - Write whatever you like in your MS~Space.
Note: This form is for use in this room only.
Would you like to create your own Life in Spite of MS~Space? Click here.
Want to find more like Jodi's MS~Space, follow this link.
"Life in Spite of MS is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com. We're also part of the Ebay Partner Network, another affiliate program."
We'd also like you to know it doesn't cost one cent more when you click through the links here on our blog. Not one single penny. And we will make a little extra cash when you do click through. We'll be ever so appreciative. You also have our word that we'll only link to things that we would use ourselves, (or wish we could have or use).
Cir & Akrista
You are reading original content written by Akrista or Cir L'Bert of Life in Spite of MS. If you enjoyed reading this blog, please consider following us on Facebook, Twitter, Pinterest, and Instagram. See you there!
New! CommentsHave your say about what you just read! Leave me a comment in the box below.