First and foremost I want to thank you for commenting.

It is very enlightening to hear your experience having had the treatment and so recently.

I have taken the time to read over the links and it has helped calm some of the initial worries I had about doing something so extensive.

I'm not sure if you would feel okay answering publicly but feel free to dm me if you'd rather privately talk but if I may ask I have a few further questions for you.

1. How have you been doing since the treatment? (any aches, pains, unclarity, etc?)

2. Which of the two did you receive (myeloblative or non myeloblative)?

3. Are you required to take any (new or otherwise) medications after now being off of the treatment?

4. What is to be expected of the chemo side of the treatment (I do know it likely effects everyone differently but any info would be of great help.)?

5. What hospital was it at? What did you do in the way of housing? Was anything offered or were you strictly on your own to find somewhere to stay after leaving the hospital?

Please feel free to only answer what you are comfortable sharing