https://laurelinobrien.com/2017/10/31/post-hsct-stem-cells-for-multiple-sclerosis-10-months/
me
There is no Rod Serling here.
https://laurelinobrien.com/2017/10/16/there-is-no-rod-serling-here/
I am from the town that is home of the Rod Serling. Yet the Arts have died here. It is a sadness that fills me with despair to the utmost. It is hard to be an artist in this town.
Post hsct stem cells for multiple sclerosis 10 months
It has been ten months since I received a stem cell transplant in Mexico for multiple sclerosis. This Saturday and the following Saturday I have to MRI set up. We shall see then if stem cells have stopped the progress of multiple sclerosis. It would be great if some of the multiple sclerosis plaques have died. Although they tell me that that takes years but I am hopeful. I have been feeling much better. My immune system has grown and I look forward to getting all my vaccines in December and then I won’t be so afraid to leave my house. I live in New York. In our state vaccines have to be up to today so I am not too afraid. If I lived in California I would not leave my house at all as vaccines are not mandatory in such States. Meantime I am just biding my time and waiting. I know they are working my strength is better everyday. My balance is not. I can stand and hold onto a cane but then I cannot move from their due to my balance. I have to just wait for new neural Pathways to grow to my inner ear where your balance is affected. I am starting to get Cabin Fever. I want to be out and about. I want to visit my old friends. I want my life back. I have faith that I will get it back. I just don’t know when. Anyone who gets themselves it is a waiting game. As my multiple sclerosis is Progressive and I have been diagnosed for over 20 years it will take some time to get back to normal. I am above Baseline. Baseline is where you regularly are in your disease. As I am above Baseline I am hoping that my MRIs will show some good results. All I can do is wait. Be patient. And continue to have faith in it has been 10 months since I received them cell transplant in Mexico for multiple sclerosis this Saturday and the following Saturday I have to MRI set up we shall see then if stem cells have stopped the progress of multiples LaRosa’s it would be great if some of the multiple sclerosis black have died although they tell me that that takes years but I am hopeful I have been feeling much better my immune system has grown and I look forward to getting all my vaccines in December and then I won’t be so afraid to leave my house I live in New York in our state vaccines has to be up today so I am Not too afraid if I lived in California I would not leave my house at all as vaccines are not mandatory and sucks state meantime I am just biding my time and waiting I know they are working my strength is better everyday my balance is not I can stand and hold onto a pain but then I cannot move from there do to my balance I have to just wait for nooner old pathways to grow to my inner ear where your balance is affected I am starting to get cabin fever I want to be out and about I want to visit my old friends I want my life back I have faith that I will get it back I just don’t know when anyone who gets themselves it is a waiting game is my multiple sclerosis is progressive and I have been diagnosed for over 20 years it will take some time to get back to normal I am above baseline baseline is where you regularly are in your disease as I am above baseline I am hoping that my MRI’s will show some good results all I can do is wait be patient and continue to have faith in the treatment I apologize for any grammatical errors in this post. I still must use a voice application and it often messes up. I wish you all happiness and good health. And I shall keep you posted as to the results of my MRI. Everyone keep your fingers crossed for me.
Peace and love Laurelin🌻

Who’s eyes?
https://laurelinobrien.com/whos-eyes/
What is your reality? Do you ever wonder what it would be if you saw through someone else’s eyes? Let’s go on a poetic journey to discover what it would be like

My reality is mine
https://laurelinobrien.com/2442-2/
People seem to be baffled by my previous post about my ex-boyfriend’s. My past is my past not yours. I can say what I want about my own past and with that let’s go on a poetic Journey as to why this is so.

Sorry ex-boyfriends
https://laurelinobrien.com/sorry-ex-boyfriends/

Parting is such sweet sorrow
We
https://laurelinobrien.com/we/
Poetry is a wonderful thing because you can express your feelings immediately. The problem is ;when you go back to post it and you no longer feel that way. That is the great thing about poetry. Good or bad. The emotion is eternalized.


I am the egg
I am the egg
My name comes from the JRR Tolkien book The silmarillion. If you know the story, you know that I am the tree that brings light to Middle-earth. If you know the story of The Hobbit then you know the riddle about the egg.” Treasure without hinges lock or Lid, yet golden treasure inside is hid.” I am the egg. If you know the story about water. Then you have heard that if you put a soft egg in water it becomes hard. If you put a hard pasta in water it becomes soft. If you put coffee in water it changes the water completely. You are supposed to want to be the coffee. I am the egg. The egg represents New Life. I am the egg.”I am Eggman. He is the Eggman. I Am The Walrus. CoocoochAchew” that is fine for the Beatles. You do not know who is the Eggman. But I am the egg.
Peace and love Laurelin🌻
Orange is the New Black
https://laurelinobrien.com/orange-is-the-new-black/
My life is not measured in coffee spoons. My life is measured by past secrets that I do not share. But if you watch closely you can find me on the show Orange is the New Black. Enjoy my poetic Journey



