So here you go.
Yes it can be Secondary, or it maybe an infection.
He does want me to take antibiotic for a year to clear up my chronic infection. By the end of the year I will have a hole in my intestint, woot! Maybe but I got to do what I need to do. Within a month I will know if it is an infection causing my legs to worsen or I am progressing. We shall see. Here is our entertaining video as always.Watch me
Hello All,
Been a while, my fault. We have two takes for the video as Sergei thought the first one wasn’t happy. So pick whichever one you want to see or both, suppose second one has more content. These videos shot before we have seen Dr. Burt. Lots of nervous jitters, lot of unknows to this follow up.
I also would like to remember Karen Bryan. It is hard to believe that she is gone. Scleraderma took her life, but it didn’t win over her. May she rest in peace.
So it’s been a while. Life goes on. Really don’t have much to complain about, regular ups and downs. Good days and bad days, more good than bad. When it’s bad – it is bad and it is scary but then it gets better and life is good again, watch my update. I’ll be forever grateful for having the transplants and here is my update to 2 years and nine months post stem cell transplant with Dr. Richard Burt. Love you guys, we’re always here for you!
Love Always,
Lana and Sergei
Hello everyone.
It has been now 18 months since my HSCT at the Chicago with Dr. Burt. We shot this short video from our road trip to share and talk about current happenings and just reiterate some thoughts and to answer some question too.
As always – please do not hesitate to send us your questions and comments. And even concerns, as you might have some, about HSCT and whole MS situation.
Thank you very much for watching, for talking to us and for following my journey.
Hello!
The flu has passed, really felt like Black Plague! Had fever for 6 days, walking was pretty much out of the question, see post previous to this, all the old symptoms were out to play. So! Once the fever dropped, after 6 days, I was able to recover. So here I am, I even skipped for you in the video. Life is good again!
Happy New Years!
Sergei and I wish everyone a healthy and Happy New Year! May your all dreams come true! Wishing you all never ending love, to be at peace and creativity to flow like a river! Your families to be healthy and happy!
As for the update: I am doing great guys! For four and half weeks been at the gym five days a week lifting weights. I am stronger and happier (loosing weight helps too). I am starting my new job on January 3rd, very excited, Tier 1 Automotive company, woot! Life is good and we should not waist a moment. I am forever thankful for Dr. Burt and his team.
If anyone needs to talk about HSCT, please do not hesitate to reach out to me.
Love Always,
Sergei and Lana
Hi
We been holding onto updates for whole summer, one reason or another, but it is September!
So lets start autumn with talking about how things are and also do some heavy and may be a bit non-traditional thoughts about HSCT as a cure for MS.
We will be in Chicago October 25-28 (most of the day on 28th), we would love to see everyone who is going to be there, also please see link if you would like to participate in this Faces of Auto-Immune Diseases .
If you see my post for the first time and would like to see my journey from the beginning, you can find it here Journey to there and back.
Hello peeps!
Realized today that I have not updated my blog.
Met with Dr. Burt and Dr. Balabanov last week on Wednesday.
I stressed my self out to the point where I had ice pick headaches, pain in my ear, just drove myself nuts. It was truly scary, did it work, did I do this for nothing, what if I still have active lesions and on and on. Sergei was thinking same thing, making plans for what if.
So my appointment day. I do not even remember what Dr. Burt said or asked. I just remember him sitting down and saying no new activity and old lesions shrinking. That moment I collapsed into Sergei’s arms and tears poured out. So much relief, bricks fell off my shoulders. HSCT, stem cell transplant worked, sweet words of remission. Since my diagnoses I have not been in remission, it was a relapse after a relapse. I do not have enough sufficient words to express accurately how it feels. It is surreal, I can dream of things I use to dream, I have a chance at life without limitation. Feels unreal.
Met with Dr. Balabanov next, he confirmed what Dr. Burt said, he was elated with how well I am doing. My EDSS score dropped down so significantly.
With all of those news, I do have to see a bone doctor and get an MRI on my hips. Steroids and chemo might have did them in, hip replacement is one of the options if it will be confirmed. However, I am not looking to do it until I cannot move!
The news of remission cannot darken anything, I can live with bone pain, I am not progressing, I am regressing 🙂
So news are fantastic!
Thank you to everyone for your support, all the kind words,to everyone who lifted my spirits and showed me so much love, Thank you!!!
Hello!
We are going to be in Chicago on Monday the 21st of this month until Wednesday for 5 months follow up with Dr. Burt. A month ago new symptoms started to come out, feels like a relapse, but who knows! So, got a call from Dr. Burt and he asked me to come in. So here I come! While we are there would love to meet anyone and everyone who is there in Chicago. Please, see the video and leave a comment if you are available or would like us to come by.
Also some additional links that we speak of in the video:
http://www.facebook.com/facesofmultiplesclerosis/ (this is for all auto-immune decease not just MS
http://www.facebook.com/events/1707002529517763/
So…4 months post HSCT. I think for a lot of people, can’t speak for everyone, issues do come out after month 3. I happen to be one of them. Perhaps it is due to steroids wearing off or chemo, I don’t know, it is not my field of expertise but it does happen. My balance has started to shift again, the gate of a puppy or a baby, looks funny. Legs feel like led, by the end of the day I truly do not want to move. The crazy fatigue is back into it’s full force, some days it is truly worse then others. UTI is back, woot! I suffered from incurable UTI prior to transplant, and seriously it was incurable, I could take huge dosages of antibiotics for it to return in two weeks time at best. So here we go again!
I am going back to Chicago this month to see Dr. Burt. He called me out of the blue asking me questions and wants to see me now, to evaluate the current situation, lets hope this is not a relapse, hope…
But hey, it’s life, it throws curve balls at you and I take it, one hit after another, sometimes I even come out stronger, and sometimes it takes me down, down on my knees, whipping, begging for it to stop. Bring it, I take it, I can do it all, right? Yeah…sometimes I can. We are all allowed to be weak once in a while, otherwise, we fight, we move forward and we make lemonade out of lemons.
Love Always,
Lana