My name is Zoleeta and I was diagnosed with Relapse-Remitting MS April 21, 2015.
I am a 27 WAH mom to a beautiful 5 year old daughter, Luna. She is my world.
I live in a rural area of Texas about 45 minutes east of Waco. I don't really have any support groups and no one really understands what MS is and that can get very frustrating.
I look forward to meeting new people and making new friends!
Thank you for reading!
Written by
zmyerswest
To view profiles and participate in discussions please or .
Hey Zoleeta, my name isBrandi I'm 34 and I found out I had Relapse-Remitting MS back in 2001 & I have a 12 year old daughter and I live inGeorgetown which is like 30 minutes from Waco. I think your the first person I have talked to that was this close to my town. 😃
zmyerswest Welcome to the group. My name is Judi and I have two teenage kids. I'm from Sycamore Illinois. I was diagnosed this September with MS. This is a great group to be part of.😊
Hi zmyerswest and Welcome to our roller coaster ride! Like erash said you now have a support group. And from the looks of it some ppl that might be close to you. But someone is usally around on here So please feel free to jump in anytime.
A 5 yr old, she will keep you busy that's for sure :D, l remember vaguely when mine were that little, they are much older now. Lol My grandchildren are 6 and 7 ♡ ugh lm old hahaha. She must be so excited about Christmas.
As you can tell we talk about pretty much anything and everything here. But most of all give each other support Welcome again. And jump in anywhere! Or just ask, someone might have an answer for you. We are all in this together. ♡
Good morning Zoleeta, it is Fancy1959, a Community Ambassador, welcoming you to this incredible chat room. You have found dozens of people to talk to and who will listen. We are all on this same bumpy, rough, and curving road that MS leads us down. Somewhere in this chat room there will be fellow MSers that have faced or are facing the same problems you are. There are so many different people here and each will give you a different perspective and solutions to how they solved the problem you're having. You of course always have to put your doctors opinion and solution for problems you're having up in the front of your mind. Sometimes we simply give you common sense solutions and tricks we have learned to ease the problems that MS is causing.
We have become more of a family than a chat room. We would love to invite you to join our family and have dozens of people to talk to, laugh with, and cry with when times get tough. You will find that together we are so much stronger. I would like to invite you to become an MS Warrior. As an MS Warrior we never give up and we never give in to our MS. We simply fight on. So Zoleeta, join us as we fight our common enemy, MS, like a warrior! Fight on!
Hi, Zoleeta and welcome to this fabulous site. I was diagnosed with RRMS at age 57. My children were grown but it did manage to rob me of my career. However, I am still learning to cope even after 6 yrs. And while my husband tries very hard to understand, he has his own problems and I find it very useful to talk with others who actually walk in your shoes. Just when you think that you are suffering from a symptom that nobody else has ever had or that you are going absolutely crazy because your fingers are so numb that you can't feel them, you can just go here and you will find lots of other MS warriors who do have the same symptoms and how they have dealt with it. I feel as if these people are my friends and they really do understand!
Welcome home! This group of great folks will seem like family soon! I found these lovely people to be a wonderful source of support, information, and encouragement.
Hi Zoleeta, my name is Shaena. I'm 32 years old and live in Cleveland, OH with my 4 year old little girl, Taylor. I was diagnosed with MS on the 8th of this month but I've feared for many years that I had this disease. It reached a point recently where I had to go to the hospital and that's when I was finally diagnosed. So far I This place is new to me and seems to be a great support group/space. I hope that you look around and that you begin to enjoy it as much as I have so far!
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.