Posted by Kelly on Feb 15th 2014

About Kelly

KLWELLNESS is open, Part 1

Welcome to!

This is a place to come and get information about wellness products that will help you in your daily life. I am an active user of CBD and doTerra essential oils and supplements. So much so, that I can’t imagine my life without them!

I have been waiting for almost 3 months to get this site up and running. While getting it ready, I have been using the products I sell. Since I am just starting out, I do have some dropshippers. However, they are all in the United States, so it won’t take long to get your products. Go USA!

You can trust in the products I sell and the truthfulness of this website. You and I are here to work together. I am always looking for the best all natural products to make our lives better.

A little about me. Well, first my name is Kelly and welcome! Right after my 21st birthday, I was diagnosed with (RRMS) Multiple Sclerosis. It runs in my family. Researchers studied our family and found the link that it can be passed through generations and family genes.

My first symptom was optic neuritis in my left eye. I went to the University of Michigan for testing and was diagnosed after an MRI. I decided not to go on medication because I just turned 21 and didn’t want to worry about it. Three months later, I got optic neuritis in the right eye. At that point, I decided to go onBetaSeron. Man was that a miserable time! I administered shots every other day on different points of my body. I had welts and areas where my muscle would dip from the shots. I had flu like symptoms every time I had to administer the shot, that would last all day. I was just miserable! I hated it and went through the “why me Lord” stage. I stopped taking the shots. I just couldn’t bring myself to do it anymore.

Next, I triedCopaxone. That was better, but after a year I would take the shot and feel like I couldn’t breathe. I would get all flushed and hot and thought I was dying! I couldn’t understand why it was happening after all that time.

So, onto the next treatment,Tysabri. This one was an infusion once a month. I had no side effects and felt so much better. Sometimes I did get a headache but I could handle that after all of the other treatments I had done. I was on this treatment for 4 years and then tested positive for the JC Virus. I had to come off or riskPML. So back to square one again. Coming off Tysabri was very hard as I felt like it was the one MS medication I could handle. It has also shown signs that my lesions were getting smaller. This was a big blow.

I relapsed big time coming off Tysabri. It was to the point where my doctor sat my husband and I down and said she wasn’t sure I was going to get better. By this point we had four kids. Two biological and two adopted. We are a busy family and I couldn’t affordNOT to get better.

Lastly, cameGilenya. It was like Ahhhhh, finally a pill that I can take. After physical therapy and steroids I was back to my old self. Running my family again. Gilenya seems to be my MS medication for life.