
This is the apheresis machine that will filter my blood and remove the stem cells. It will filter my entire blood volume twice before it is finished.
So here’s what will happen, they will hook me up to this machine through the central line they have inserted into my neck. It will run for about 5 hours and it will cycle my blood through, and separate out my stem cells from the blood and return the blood to my body. This process will happen twice, I’m told.
The goal for today to to get 2 million stem cells per kg. of body weight. I won’t go into exact numbers for obvious reasons. A lady has to have some secrets right? There are three of us doing stem cell collection today, and I’m hoping we all get our stem cells in one shot. I won’t be terribly upset if I don’t get them all. Its not uncommon for people to take two days and sometimes even three days.

Not for the feint of heart. You can see the stem cells collecting in the bag on the front. Doesn’t look like much yet, but wait….
First thing, Dr. Federenko came in and set up the machine. He organized all the tubing and made sure the machine was in working order. Then Nikolai came in and hooked me up and got things going. Incidentally he was the same guy who did my hair cut the day before.
There is a very short cord on this machine so there really is nothing much for any of us to do while this process is going on except lie in bed. Which makes going to the bathroom a bit of a challenge. You really have two choices. You can either hold it or you can use the diaper they make you wear. Yes they give you a diaper. No secrets here. I have always said this would be full disclosure. But for the record, I managed to hold it. I think the key here was I drank nothing in the morning and didn’t even have breakfast. I waited on all of that until the process was done. It wasn’t easy as it actually took 6 hours rather than the 5 I was told. But I made it. Yay for me!

My husband Dan has been through so much. I wore his DANSTRONG shirt to give me the strength and energy to get through this day! It worked!
When everything was said and done, Nikolai came and started to break down the machine. There was one little bag of what he said were my stem cells. It didn’t look like much to me and I was a bit worried, but there was nothing I could do about it at this point. All signs had pointed to good collection. I had bone pain the prior three nights which said to me that stem cels were moving through the bones to the bloodstream. But still that little bag made me a little nervous. My friends said they would wait a day for me if I didn’t make it, and that was a nice gesture.
Now we just had to wait. After they collect the stem cells, they send them off to two different labs to confirm numbers. I was so tired that all I wanted to do was sleep. My sister got me a little fan at the Russian version of our 99 cent store and that helped me take a nap as I was really warm. It seemed like no time had passed when Dr. Federenko came in to tell me that not only had I collected enough stem cells, my entire team made their numbers as well! We would all be starting Chemotherapy tomorrow!
One last thing which was a bonus for getting all our stem cels is that we got our central lines removed! Sounds great and it was. Only thing is we get new lines the next day for the chemo. But that is alright. The new lines are thinner and more flexible and hopefully more comfortable. I did insist on seeing this thing after it was removed though. It was HUGE!!!

Well there it is, the central line! I am happy it is gone. I won’t miss it. Getting a new one tomorrow but Im sure it will be much better. Its a means to an end. An end to MS!
I was very happy with 2.1 million stem cells per kg. My friend Kim got 2.4 million and that bastard Bill got 4.8 million! He is an over achiever but we love that Aussie Bloke! Good for all of us. And it’s the best 3rd place finish I have ever had. Ill take it! We have all made it, and now move on the the heart of the matter, Chemotherapy. As they say, Chemo is the Key. Chemotherapy will be killing off the bad parts of our immune system and the stem cells simply help us to rebuild a new one without all the bad stuff. Here’s looking forward to Chemo!
Congrats on today’s collection. I am so excited for you. Now time to Let It Go ?❄?
Way to go Laurie -you can do this!! Bye bye MS!!
Fight on my love. Soon we will be back together and starting a new cancer free and MS free or as close to free as possible.
Sending you all my love and strength.
Love you and miss you every day! I can’t wait to be back home in your arms! I love you to infinity!
You are so brave. I hate needles and almost pass out. I was hyperventilating just reading about your procedures. Hang in there, we are all praying for you and Dan.
So proud of you! Great job on those stem cells! Should have taken a bottle of
“Skella-grow “with you perhaps it might have helped… Can’t wait to meet these crazy Aussies, I’m so glad you have each other. Cheers to all of you.
Lol I forgot the Skel-grow but I guess I didn’t need it anyway! Thank you friend! Can’t wait to see you in Moscow to bring me home!
You are amazing!!! You are constantly in my thoughts!! You are a badass!!
Love you girlie! Thank you for the strength you send. This has not been a walk in the park but it will be totally worth it. When I get back and can have visitors, I would love to see you and give you the first hand info!
Congrats Laurie! I am so glad everything is progressing with your treatment. I have a neighbor with MS that is too advanced for any treatment at all. She and her husband are both praying for you. She is so sweet and is rooting for you to kick booty!! Tell MA I said hi. Sending prayers for you and your hubby. 🙂
Thank You Karen! I am confident this will work. This Doctor is know world wide and had been doing this for over 15 years for autoimmune diseases. If only the United States could get things done faster. It’s such a shame as this is a cancer treatment we use every day and have been doing in the states since the 1960’s. But when there is some kind of “off lable” use, the FDA gets all up in arms and requires trials. This won’t be available in the US for Autoimmune diseases for another 5-7 years sadly. I just couldn’t wait any longer.
Laurie, you are a rockstar! Been praying for you nonstop. And BTW, as one of your “hair challenged” friends, I say good riddance. It will grow back thicker and fuller. Hope you feel the love from LA.