HSCT Journals
My Newest Blog Post
Ten Months Post Transplant: Mesenchymal Stem Cell Therapy at Hope Biosciences
I know this is a long blog, but there's a lot to share. It was another early start with a 2:30am alarm to catch a 6am flight out of Redmond, OR to Houston, TX. As soon as I landed at IAH, my dear friend Amanda picked me up and we went straight to Hope Biosciences...
Written by Jenny Angus
Subscribe to my blog
More From This Category
Walking Video 5 Months Post HSCT + Update
This last month has been very, very challenging. I made a big change in effort to try and find a better way to live, and to further rehabilitation. I have experienced a few extreme (but short lived) drops in functionality, return of two bad symptoms, combined with all...
Walking Video 4 Months Post HSCT and MRI Update, etc…
This past week has been really tough for me. Most of it stemmed from the impassable walls I slam up against as a disabled person trying to do something to help myself, or for myself. We’ve all seen those videos where cars are being tested, sent at full speed crashing...
Preparing for MRI Trip: June 8th
I’ve spent the last month stressing, thinking, wondering who might be able to take me to the city for my yearly MRI yesterday. Luckily a week ago a kind friend offered to take me (I almost cried in relief). She had a few errands herself so it was a win-win. It’s a 2.5...
Jenny when do you go?
Hi Janet, I leave Jan 30th.
Hi Jenny, i live in Germany and the neuros tell me I am too old for HSCT st 54 and my MS is too far gone.. The German MS society is also useless. So is My husband.
How did you manage to get to Mexico
All the best, Bernadette
Hi Bernadette, So sorry to hear of your situ. I think the first step is to contact Clinica Ruiz and begin the process to see if it’s something you want to pursue. It’s your choice and your life. When you decide, then next step is to figure out how to pay for it, and then physically get there. Here’s a link to an article I wrote on my decision making process. I hope you find relief. Kindest regards, Jenny
https://multiplesclerosis.net/living-with-ms/hsct-decision