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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February 24th: +7 Transplant
I had another night of unexpected sweats (gah, again!), constant disruptions, etc. I guess I have to get used to the idea them coming and going at whim. I realized that eight years ago today I was admitted to the ER and later hospitalized as a result of my MS. I...
February 22/23: +5/+6 Transplant
I have combined these days to catch up. Tuesday was largely uneventful with the exception that it was ‘22022022’. It took Fernie pointing that out for me to rise out of my dazed state to recognize the symbolism. Cool. I had a bit of a break in the intensity of all my...
February 21: +4 Transplant
OK, here’s my update, albeit two days behind and late in the day posting. I had to wait today for pain control to kick in for a post-spinal tap like crushing headache that hit me this morning. ___ Unfortunately, I’m not sleeping much as a side effect of the...
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