http://www.hopkinsmedicine.org/hmn/W08/feature1.cfm
Unfortunately, his MS has not been well behaved, but fortunately, it is therefore more likely to respond to this therapy. So far, half of the patients without taking medications afterwards have a sustained remission. Now, patients are taking Copaxone afterwards, which can act like a vaccine against MS, at least in mice and monkeys. In those patients, ALL are in a sustained remission at the 2 year mark.
He'll be getting 4 days of cyclophosphamide, a chemo drug, and it'll kill all (or at least 99.9999%) the immune cells that have been made during his life so far. It'll leave his stem cells intact, and they will reconstitute his immune system from scratch.
So this is where I fit in- I'll be cleaning like crazy, (which btw, is against my innate nature), giving meds and making whatever food sounds palatable. I will even give foot rubs, but this is a special occasion. We'll have the help of many people, of course, including our families who are coming to help out, and our local area friends, Adrienne and James, who got us our sweet diggs and are loaning their car. THANKS GUYS!
So, this week, I will be anticipating any childproofing needs (outlet plugs, thick padding, etc.) and getting packed. We'll get in on Monday, and will start the procedure on Wednesday. I'll keep this updated, so that you too can feel sympathy for nausea and vomiting, but also feel jealous of his sweet medications.
10 comments:
Good luck Lembergs! I'll be thinking of you! --Love, Avanti
Today the packing began and Mary advised me that I will not have to fear enduring fresh fruits and veggies starting soon. Whew! I was worried I might have to start eating healthy.As for packing, it has never been easier - sweat pants and t-shirts and presto! Well, with my cold wearing on I will be lucky to start the infusion on Wed at all. Thanks to any of you who are out there paying attention. Love equals awareness + compassion and it is good to have so much of both around.
Tchau,
Blake
Looking forward to seeing you both. Have a safe trip out and I'll see you Monday night.
Hey Guys,
Thanks for the update. I can't believe it is already here. So, I just finished an exhausting month on the hematology service and have seen a few hundred people undergo chemo and what I realized is that no one reacts to it the same. Also with modern day anti-emetics, benedryl, and antibiotics, it seems to be tolerated fairly well by most.. especially the young patients. It really depends a lot on your attitude. Really try to keep eating as much as possible and be as active as possible, b/c it really makes a big difference, especially when you need the energy to run away from Mary when she becomes too overprotective. JK. Well we love you both and we'll keep you in our prayers. Keep us updated.
Carole
This is so cool that you have started this blog. I will be checking it religiously and thinking of all three of you in my prayers.
Our thoughts go with on this journey. Good Luck and God's Speed!
Hope you had a happy landing in Baltimore. Blake, I hope you are not suffering from anxiety as you begin the treatment course. Thinking of you all the time. Bess said she talked to you Sunday and your cold was going away but you wondered if it could delay your treatment. As I particularly feel the need of prayer now for you I am happy to report we have a new Priest in Byron as of Nov. 23rd,and he is joyous. Grant and I really liked him. (Bess had a cold and stayed home) Mary, this was a great idea. Thank you for all your hard work on Blakes behalf, Mary. God bless you all.Katherine.
Blake,
Marisa and I send our positive thoughts in your direction. Thanks for keeping us informed on your adventures toward wellness. Love, Tom/Marisa/Ebi
Hi Mary, Blake and Alden, I figure you may want something to read to skip the time of waiting for tomorrow to come.... I think sooner then you know you will be back home again and getting back to your old you :o) We are thinking off all of you. Love, Chet, Luzia and Thailan
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