10 months post hsct transplant for multiple sclerosis.


Wanted to give you all a wonderful update on how I am doing since my stem cell transplant.


10 months post hsct transplant for multiple sclerosis.

My doctor in Mexico said that I would start to really noticed results at about 10 months. He was correct. I am no longer sick every day as my immune system has greatly grown in strength. But every day now I wake up with more strength. Every day I can do something I couldn’t do the day before. My bowls and my bladder work now. Only on occasion do I have difficulty. I have enough strength that I can stand on my own. I can always get in and out of bed and in and out of chairs. My entire life has gotten better. Once I have all my vaccines in December I will be more comfortable going out and about. I have be gone to explore promoting my poetry around my area. I plan on holding an EDM event for my stem cells in May. Life is looking brighter and brighter every moment. And I am not taking it for granted. And I am so grateful. I am I so keeping up with the Spanish skills that I incurred in Mexico. Absolutely walk right now if I had balance. Unfortunately the lack of balance I have is due to the inner ear which is nothing that stem cells can fix. However you can grow new neural Pathways. And that’s what I have to do is just wait for new neural Pathways to grow. And I have no doubt that they will. Stem cells have absolutely been a success. Please anyone that has a disease that can be treated by stem cells please seek out this method. Don’t let the pharmaceutical companies control your life anymore. I’m so grateful and I am so blessed to tell you today that I am getting stronger and better. I wish good health to you all..

Peace and love  Laurelin🌻

8 months post stem cell treatment for multiple sclerosis.


A quick look at how I am doing 8 months after receiving my stem cell transplant for multiple sclerosis in Mexico. On a more personal note I found the Mexican people to be much more inviting and kind than most Americans I have met. But Build That Wall number 45! Mexico only gets most of their corn from America you just put a lot of farmers out of business. Go number 45!

8 months post hsct stem cell transplant

I am always sick as my immune system grows new antibodies. However ,it is getting less and today I don’t feel like I have a cold. It has been an up-and-down roller-coaster of my multiple sclerosis being better, than my multiple sclerosis being worse, and back and forth over and over again. But that’s exactly what’s supposed to happen. My bladder and bowels finally do work. That alone is a miracle. You guys have always worn underwear but trust me wearing depends sucks all the time. But now I get to wear that wonderful breathable cotton underwear. In December it will be my 1 year and I’m sure I will see even better results after one year. That is one I can get my MMR and chicken pox vaccines. For now I just have to be patient and wait for my white blood cells to divide and grow stronger. I am having a new life party in October in Binghamton and I looking forward to that. I am at the start of a new life. It’s kind of weird I always knew I died of complications due to multiple sclerosis. Now I have no idea how I’m going to die. And I think that’s the way it’s supposed to be. Because it sure makes me feel better. I am on a lot of steroids and still getting some chemotherapy but a very low dose and the steroids do make me a little bit crazy so I’m trying to only stay on my blog site. If you’re ever in the Binghamton area stop by my party Beautiful Dreamer. However I know some of you live in India and turkey and I certainly don’t expect you can make it. 🙂 I can’t wait for the day that I can tell you I’m walking with a cane. I will get there soon. Thanks to all who raised money to get me stem cells. Now I just have to wait. Patience is a virtue.one I dislike very much.