12.30.2010
The Muckelvene Tribute...we Thank you Ja!
12.29.2010
WF4HC messages....please donate to WF4HC for those fighting Sarcomatoid Carcinoma of the Prostate as well as Prostate Cancer.
To: princessjamecia@yahoo.com
Sent: Thu, December 9, 2010 3:03:12 PM
Subject: Give hope ...
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I'm not trying to be rude, but I'm not sure how you all are helping us who are fighting Sarcomatoid Carcinoma. If you can email me back and tell me what hope you have given our family. I would greatly appreciate it. I'm course to find out what hope you all or research or funding goes towards folks fighting Sarcomatoid Carcinoma of the Prostate. Maybe I'm missing something. Please let me know how you can help our family.
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Thank you for reaching out to your American Cancer Society with your concern. I will be happy to look into your question. We will contact you as soon as possible regarding available information on research funding for Sarcomatoid Carcinoma (of the Prostate).
Please know that our Cancer Information Specialists are here to address questions about diagnosis and treatment related questions, as well as support resources anytime 24 hours a day/7 days a week at 1-800-227-2345 or via "contact us" at www.cancer.org.
Thank you again.
My best to you and your family,
Hello again,
I have received further clarification regarding your question on our research funding for Sarcomatoid Carcinoma of the Prostate. The Society is currently funding 98 grants dealing with Prostate Cancer totaling $53,812,500.00; however, none of them specifically involve Sarcomatoid Carcinoma of the prostate.
Please let us know if you have further questions or needs related to this diagnosis by calling 1-800-227-2345 anytime 24 hours a day to speak to one of our Cancer Information Specialists, or via "contact us" at the bottom of our home page at www.cancer.org. Our specialists can assist with many needs such as locating area support groups, transportation to treatment appointments, and answering questions related to cancer treatment and its side effects.
Best,
This is why WF4HC is needed. Please donate to our cause.
Benefit Concerts
12.25.2010
Daddy's Celebration of Life Services You can also donate to WF4HC
Facts
Born: October 24, 1952
Place of Birth: Norfolk
Death: December 20, 2010
Place of Death: Upper Marlboro
Occupation: Co-Founder & President WF4HC
Hobbies: Loving Pearl (His Wife), ALWAYS & FOREVER, Spending time with family, Reading the Bible, Gardening, Bowling, and Sketching.
Organizations: Warriors Fighting For HIS Cure, Inc. (WF4HC)
James I. Muckelvene
October 24, 1952 - December 20, 2010
Wake
Monday December 27, 2010, 10:30am - 11:30am
Spirit of Faith
South Location
Celebration Of Life
Monday December 27, 2010, 11:30am
Spirit of Faith
South Location
Service Honoring 20 yr Veteran
Monday December 27, 2010, 2:00pm - 2:30pm
Cheltenham Veterans Cemetery
Donations
Warriors Fighting for HIS Cure, Inc James "Rudy" Muckelvene, Co-Founder & President
Sign the Guestbook
Share your thoughts and memories about James I. Muckelvene in the guestbook.
12.15.2010
Thriller
12.13.2010
Blessed
Last month I received an e-mail from Ronda, I believe I posted her e-mail on the blog. Ronda dealt with something similar and feels a personal connection to our story. There are a lot of similarities in our stories and we too feel a connection with her.
Last week her husband Keith James ( http://www.chefupnorth.com/ ) who is a MAGNIFICENT chef that owns a catering company prepared and delivered 10 COMPLETE MEALS for my father. A family that we had NEVER met but felt connected and wanted to help took the time to deliver and cook 10 MEALS for my Dad. If that is not amazing, I don't know what is.
My dad was ALL smiles when they brought the meals to him. I have been the main "chef" since my father was diagnosed and I do OK :) After each of Keith's meals I asked my dad "how was it?" and he said "it was REALLY good! It was well seasoned and tender. It was good!" Normally after one of my meals I ask "how was it?" and he says *long pause* "it was pretty good"
ON TOP OF THAT... Ronda and her husband INSISTED that we contact them when the meals run out and offered to make my dad even more.
12.07.2010
This Is My Daddy
Pended post from 12/7/2010
12.03.2010
Art is Therapy
12.02.2010
SARCOMATOID CARCINOMA
"Our Mom has been recently dx with the following listed above- We need as much info as anyone can provide, there are so many mixed messages and treatments , however we are aware it is not curable per the CA Doc but non the less-we want to make the right choices and decisions as far as treatment vs non treatment for her - Some has listed that the tumors dissapear and in some cases they have with our Mom but have come back with a vengance - Recently she was rushed to ER due to tumor ruptured the spleen and she was bleeding out, according to the docs this never happens except in Leukemia patients but it did for her.. Testing has been ongoing since March of last year , Mom went in for Cataracts and the Doc she saw insisted on a chest X-ray before they went any further , am unsure why but almost a year later and multi biospys of the lungs and lymph nodes int he center of the chest, pulmonologist were certain it was not cancer until Dec another CT was done and a tumor showed in the adrenal gland along within the areas of the liver and spleen, also a lymph node under the arm had been causing her pain- Upon biopsy approx 3 weeks ago of the arm lympoh node the Dx was made and then a week later the spleen ruptured.. We have been advised this is an aggressive Ca , and is not curable but I have read cases where after chemo and or removal of the tumors that some have had a 5 year servival rate and unfortunaly the majority of cases I have seen and or read have been where our Mom is at now - Since being home , she sleeps alot except for a night - is uncomfortable , denies pain but you can see that shes in pain- nothing tastes right to her so no appeitite to speak of , has lost alot of weight already due to not eating- she has stomache upset alot - We are frustrated with the docotors, althought this being a rare Ca ,I dodnt beleive there is enough info on it and or out there , we are still waiting on further from Mayo on the first biopsy but for now this was the dx given.. Mom has alwasy been healty , never ill , never in hospitals - it so insanley wrong to see someone so well and then a matter of hours and weeks , its gone - I am angry , I know it is one of the steps but I dont understand the technology they have now it just blows me aways that no one knows anything ( the Doctors)