HSCT Journals
My Newest Blog Post
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...

Written by Jenny Angus
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More From This Category
Coping During HSCT & Walking Video 4 Weeks Post
Many people find HSCT challenging for obvious reasons, but also because there are blocks of time when for some it can be unbearably boring and isolating. These periods occur when we are confined to our rooms waiting for our blood counts to increase. However, I was...
Walking Video: Two Weeks Post Return Home
These last six weeks have felt like forever. An immense amount has happened, the incredible transformations both up/down, and the full range of emotions I've experienced are something unparalleled to any experience in my life, to date. It's exactly two weeks ago today...
Thank You’s & HSCT Recovery Expectations
I want to thank the many, many people who have sent through comments to me on my blog posts. I received somewhere between 200-250 messages (not including the direct notes/messages) over the course of my treatment. I have barely been able to send any thoughts or thanks...

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