HSCT Journals
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One Year Post HSCT: February 17th My Birthday
If you've seen my social media post today this is mostly a repost with the exception of a few things, especially the exciting news in one of the YouTube shorts at the bottom 🌟 Exactly a year ago today I received my stem cell transplant. It’s considered your new...
Written by Jenny Angus
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Images: Trip Hope Biosciences and Dr. Nikko Plastic Surgeon
Here are some images of Hope Biosciences and others from the Houston trip..... Amanda ❤️ Amanda, MSSagirah and me at Hope Biosciences Lobby Hope Biosciences Taking Copious Notes on the Tour These are the steps and containers used to grow the stem cells (they are...
Eligible for Mesenchymal Stem Cell Treatment at Hope Biosciences in Houston, TX
Everyone knows, I’m a science geek. I have researched how to treat my rare, unrelenting and unresponsive disease. Last February 2022, I had HSCT in hopes of ousting my Poltergeist. I will forever be indebted to everyone for funding me for that. It is a two year...
Six Months Post HSCT, Reality Check & Further Walking Improvements
These last months have been unreal, amazing, and as always, challenging. I could write a full blog about the challenging parts, brutal days, symptoms overload, mental aspects and emotional impacts of all that, so I’ll just leave it at that for now and move on…. For...
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