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Report from Curt
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Dear Folks,
hello.Thank you for your notes, messages, support,unfortunately, Curt is unable to respond. Report from Curt Miller via Elizabeth , his wife.. Curt finished his 1st chemotherapy at 2am June 10, Sunday.We are wawiting result, response of the treatment. He had 2 units of blood for his low blood count from his infection and chemotherapy. He did have 2 okay days before his not so okay day last night with fever ,shaking chills and vomiting. I am waiting for positive results from his therapy. Yours, Elizabeth PS Love to all from Curt. Posted on 06/16/12, 02:32 pm |
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Bumping back to the top. 
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glad Cathi, you bumped back to the top... Have been wondering how Curt is doing... continued prayers for him and his family.
Annette
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Same here. Sending much love and prayers to he and Elizabeth. Carla
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Thinking of you Curt...
TJ
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Hello.I am Curt's wife ,Elizabeth and I have been with him daily for the past 50 days until July 17.
We had his funeral memorial rmembrance yesterday,July 20th. This group is important to him that he gave me access to the site. I was consoled with the entries in the guest book from the online newspaper, http://www.legacy.com/obituaries/ti... Yes, he would talked about the different therapy and medication of MG. He continued the updates as long as he was able. He had just finished his 2nd chemotherapy on July 7th.for his lymphoma. July 11th, we enjoyed a DVD movie at the bedside. He was enjoying being out of bed July 12th.Over the weekend,he required more mestinon and prednisone.after evaluation by the neurologist. His final diagnoses were the lack of WBC from his chemotherapy, pneumonia and lymphoma. Curt was still responsive to my hugs, kisses with a smile and kisses. July 16pm. I shall miss the Curt that I love. Thank you. Yours, Elizabeth Mei Wong EMWBoston@comcast.net
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My thoughts and prayers go out to his family. i didnt know him that well. but i did read most of his post when i logged in here. it breaks my heart to hear of his passing. im so glad to have joined this group this is one of my first actual support groups that i found when i first learned of my lil girl being diagnosed with mg. and i tell myself over and over that i will do everything i can to help bring more awareness not only for my daughter but others who are fighting this disease. you are all so amazing and im glad to be a part of this MG FAMILY
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