Today I get stem cells today is my birthday

It’s 6:52 a.m. in the morning in Mexico and I can’t sleep another wink. I am so excited to get stem cells at 11 o’clock a.m. this morning. This will be the beginning of my new life. Truly it is my birthday. I have gone through a lot of pain and anguish to get here. Including four doses of chemotherapy many shots that I don’t know what they are called and many pills that I don’t know what they are called either.

This is a picture of them harvesting my Stem  cells. After the fourth round of chemo my immune system is officially dead. And my multiple sclerosis does seem much better. I have much more strength but unfortunately you do need an immune system to survive so hopefully if the stem cells will grow quickly and I will have a new immune system without multiple sclerosis. I do have an AEDS  score of 6.5. I am lucky because after you are in 8 you are basically not eligible for stem cells and are probably going to die of side effects due to multiple sclerosis. Because I lift weights ,my arm strength gave me a  instead  6.5 instead of a 7. No matter what disability did disease you have you must work on keeping the strength that you have and are able to use. It does make a huge difference. After I receive my stem cells today I will be quarantined and not able to go out into the public and be on a special diet no raw foods or vegetables and other such things. I am so excited to be home to return home to the United States and wait for my multiple sclerosis to disappear. I look forward to so much. I look forward to playing with my daughter at the park. I look forward to cleaning my house. I look forward to being the wife and the mother that I know I have always been sposed to be.

I cannot wait for all of the IVS and this pic line to be taken out of my chest . They have been extremely painful but the pain I know it’s going to be more than worth it. Clinica Ruiz in Mexico has been outstanding to us. I recommend that anyone with multiple sclerosis that can afford it go and if you can afford it do as I did and hold benefits and anything you can do to raise money. The one thing I will say about this whole process is you need to have a positive attitude. There is one person  here who has a very low score. They are  on disability and they are  still able to work a little bit. In my opinion they should look at this as a blessing many of us cannot work at all. We need to be positive in life and always we need to try to not see the negative. They have  complained about the stairs not having railings. And I’m thinking to myself, but at least you can walk! Many of us here can not walk at all  and I’m sure it is slightly insulting. If not insulting just hurtful. Instead of feeling negative about having no railings think about the fact that you have legs  that work. people need to see the positive more than the negative. People have complained about the delicious Mexican Cuisine here right in front of Mexicans and the food here is outstanding. People have complained about the delicious Mexican cuisine here right in front of Mexican and the food here is outstanding. Some people speak on there cell phone while we’re getting chemotherapy so loudly that I know just about everything in their  life.. Anyways I will not go on my point is that we need to have a positive attitude when it comes to ourselves and our illnesses and our lives. Without positivity what good is living? Negativity only brings upon more negativity we need to be blessed feel blessed and happy with what we have. And be even more blessed when something like stem cells comes along to better Our Lives. I am so looking forward to this new journey in my life it is quite amazing that I was diagnosed on my eighteenth birthday and 18 years later when I was 36 I was that I was allowed to come to the clinics Ruiz nothing is in life is a coincidence. Nothing in life should be taken for granted. We should all feel blessed and we should all find joy in our lives.. we all are so lucky just to be alive and just to be part of this wonderful thing called Humanity. I wish you all the best of luck in all of your endeavors and I can’t wait to see you all when I get home. For those of you who live out of the country I wish you all the best of luck too and remember there is always help out there somewhere. Stay positive stay strong and as always peace and love Laurelin 

Stem cells in Mexico for multiple sclerosis day 14

I have had two rounds of chemo. Which has improved my strength greatly. Showing that the immune system of those with multiple sclerosis is killing us. Today I got a PICC line and catheter in my chest. In preparation for them to take stem cells from my body. I still have to get two rounds of chemotherapy and they have to put the stem cells back in my body and then I have to hope and pray that a new immune system grows quickly before I catch a bug or a flu from someone. So far my experience has been successful. I am writing this to tell everyone with multiple sclerosis that the answer to our prayers is stem cells. If you are like me and you live in the United States of America this is not possible. It is because the United States relies heavily on pharmaceutical companies and their money. You see if I have an immune system without multiple sclerosis I do not need to be on my medications which cause hundreds of thousands of dollars a year. I implore anyone with multiple sclerosis to seek out a treatment that I have. I have decided that I am going to mainly use this blog to show how far I get with my treatment. When I began writing this blog  I was I was wheelchair-bound and could not walk. Today I can walk a few feet with a walker but I still can’t not write. I’m hoping in time my beautiful penmanship will return. As of now I have to sign my name with an X. My website is still a poetry website on my homepage but from here on out all of my blogs will be about multiple sclerosis My Success or lack thereof. Although I do not see there being any lack thereof. I also want to inform my country but there are other ways to improve your quality of life besides for taking pills. The pharmaceutical companies are trying to take over the United States of America and they are. I will keep you posted I am getting my stem cells in three days. Which I am calling my birthday as that will be the day I began begin a New Journey in life. Hopefully a life where I can hold my child. Leave my house. Wear underwear instead of Depends. Not have bladder and bowel problems. And the list goes on and on but I will not continue telling you all of my woes also, I hope that perhaps this can help people to get off their medication and to help America stop being run by pharmaceutical companies. We are the land of the free. There is no reason why stem cells are not of use in our country. The only people that can get them are certain type of cancer.. stem cells can be used to treat so many illnesses. It is ridiculous our nation has become a nation that relies heavily on money instead of taking care of the people who actually live in it. If you are anyone with a debilitating illness such as myself do not give up hope. Write your Congressman write your Senator write your governor shout to the world that we need stem cells in America. I will keep you updated on my success as I know it will be successful. And I will finally be the wife and the mother that I am meant to be.

As always peace and love do not give up hope LAURELIN 

Stem cells in Mexico day I don’t know

Finally feel up to writing a Blog

Chemo has put me in a fog.

It’s like I’m here but I’m over there.

10 more days till I lose my hair.

Have  strength back so I really don’t care.

I really don’t care if people stare.

People ignore you when you have multiple sclerosis.

They have no idea of my medicine doses.

At least maybe now people will look at me.

Cuz before it’s unpleasant for them and they just don’t want to see

I just want to feel normal and play with my kid

Bake cookies with her like my mother did.

Stem cells soon and a new life will begin.

In America fundamentalist think it’s a sin

In Mexico I am treated like a human being

They look right at me and it’s me they are  seeing

I will return better and strong

Maybe I’ll even write a song.

Healthy is where I belong

All you fundamentalists are fucking wrong

This is like a giant terrible test

But wait until you see my success

I’m young I still have things to do

Take care of me and I’ll take care of you

This is what it’s all about

Love each other and say it with a shout !

Love is what it’s all about in Mexico

I hope the new president gets it you know?

Love to you all and take care

Soon I’ll be home with love to share

Peace and love Laurelin 

Stem cells in Mexico day 5

We had yesterday free to prepare ourselves for today. I am getting chemotherapy at 1 o’clock Mexican time. On the third day of stem cells which I did not write a blog I had so many tests and was so tired that I apologize I didn’t write one I got my EDSS score on that day. If you score an 8 that means you have no hope and you are basically going to probably died of complications from multiple sclerosis. If you have a 7 they will still treat you here but you don’t have as good of luck and it may not do very much. We were hoping and praying for a six point five or a six. I prayed last night to every religion’s God to the goddess and to Nature just to cover all of my bases. And I got a 6.5! So it does look like stem cells are going to help me quite a bit. I also had a ton of lab work. They took more blood out of my body than any lab work I’ve ever had done LOL. I got to meet the doctor who actually founded the clinic and he is a wonderful wonderful man. He treated us all with such respect and made sure to meet and greet and speak with all of us. I also had lung function test and a chest x-ray. And as well as having my urine check. And for all intents and purposes other than the fact that I have multiple sclerosis I am extremely healthy! How do you spell Dr how do you say it dr. Ruiz is the doctor who founded the clinic and he is the one that we are calling Santa Claus because he is like this mythical creature that has come down from God to help all of us with multiple sclerosis. The other great thing is I have made many friends with multiple sclerosis that I am sure I will continue to stay in contact for the rest of my life. And I have learned that you have to be your own Advocate cuz I have 


Heard of drugs that could help my Tremors but no neurologist has ever suggested to me. The picture above is the man himself dr. Ruiz. He is so very kind and I suggest anyone with multiple sclerosis come here. It is much cheaper than anywhere else because the peso is not worth much money. So far I have had a very good experience except for very being very fatigued and tired. So I’m very glad they gave us yesterday off. I am hoping I am one of the 10% that doesn’t lose my hair because I have such long beautiful hair but if I lose it all it’s worth it. It is all so beautiful here in this city Puebla. It is one of the few cities in Mexico that is expanding and actually the economy is doing better than anywhere else in Mexico. I am so grateful to be here and I will keep you posted and let you know how chemotherapy goes tomorrow. After after I have chemotherapy today I have one more round of chemotherapy and then they will take stem cells from my body. Let’s all keep our fingers crossed… peace and love Laurelin 

By the way that picture is a picture of a volcano in the background can you see the steam coming out of it? It’s pretty cool. I like this town very much people are so well-mannered and polite and if that Donald Trump build the wall we will get our daughter and move here. As always peace and love my friends

Stem cells in Mexico

I’m in  Mexico preparing to get stem cells. I start chemo therapy on Friday. I’ve only been here three days and I’m so exhausted. I really hope that these stem cells help me in some way. Even if they only help me a little I’ll be happy. I don’t expect really to ever walk again but I do want my bowels and bladder problems to go away. As well as the heat and cold bothering me., I am so fatigued all the time but my hopes are high. There are so many people here that aren’t nearly as bad off as me but there are a couple that are worse. It is slightly depressing to see people here that are walking  and you are bitching about problems. I guess I just expected to see more people that are as bad off as me. But I should feel lucky and be blessed that I am here in the first place. This is my last resort and my last chance so let’s all hope and pray that it works. I start chemo therapy on Friday. I must say I am not excited to lose my very long hair. But  the hair on the rest of my body I’m pretty excited about losing. The really good thing is my Spanish is getting better. I miss my daughter and I Miss America but I don’t miss Donald Trump. I’ll keep you posted and blog  every couple days to tell you how  I’m doing. Peace and love Laurelin