HSCT Journals

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Walking Video 5 Months Post HSCT + Update

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...

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March 2nd:  Arrival Home

March 2nd: Arrival Home

Our flights on the 1st went as well as planned, although long and arduous. I drugged myself up as much as possible, and when the drugs wouldn’t shut down my overwhelming symptoms, I ordered tequila. (Yeah, yeah, I know not the best idea, but I was desperate for...

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March 1st Part II of II:  Travel Day & Goodbye to Fernie

March 1st Part II of II: Travel Day & Goodbye to Fernie

Next....off to pick up Lisa and to the airport. Thank goodness for Raul and Fernie as check in was NOT straightforward. Lisa had overextended her allotted days in Mexico and had to go to immigration in Mexico City airport to have that extended, before being allowed to...

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March 1st Part I of II:  Travel Day & Goodbye to Dr. Alex

March 1st Part I of II: Travel Day & Goodbye to Dr. Alex

Tuesday the 1st: huge day! I was suffering immensely from the infusion yesterday. To sum it up, I had little sleep last night, crushing headache, unbearable discomfort/extreme distention in my abdomen of fluid retention, same bladder issues, heart palpitations, body...

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4 Comments

  1. Janet B

    Jenny when do you go?

    Reply
    • Jenny Angus

      Hi Janet, I leave Jan 30th.

      Reply
  2. Bernadette

    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

    Reply
    • Jenny Angus

      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

      Reply

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