HSCT Journals
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My Weekly Pharma – World MS Awareness Day May 30th
Many pwMS (people with MS) live with multiple types of medications and/or use supplements to help with bodily malfunction. If you're one who doesn't use any, then I'm sure you already know you are a rarity and I'm happy for you 🙂 Aside from oral pharmaceuticals...
Written by Jenny Angus
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Guest on Podcast with FUMSNOW.com
This post is a podcast that I had the honour of being part of with my brilliant and successful friend Kathy Reagan Young, owner of FUMSNOW.com this past January. Kathy has MS as well, was forced from her career as a result of the disease. She has through her own...
February 19 (Saturday): +2 Transplant
My days are blurring one into the next. I had to look at the calendar to know I’ve been here three weeks now. I realize I am two behind in posting my blogs from my actual real time, making hard to follow. I hope to catch up this week…. As for last night, it was...
February 18th: +1 Transplant
I had a much better sleep than the day before (no rocket launchers, haha!). I felt blessed with no nausea once again. I still have a few days to get through while the Cyclosphomide is working it’s ‘magic’ in my body. You have to know my fingers/toes are triple crossed...
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