A private place for Pete Dern updates and support
That dreadful visit to the doctor. Hearing those words, "Cancerous tumor" rushed through my head and spun me into tunnel vision. My eyes immediately looked towards my husband and I seen the fear in his eyes. I knew I needed to be strong for him, but didn't know how what this mean for me, for us. I didn't how to react, how to feel. Actually numb. That about sums it up. Of course that moment changed our lives forever. We had the best doctors who took time. Talking slowly, compassionately. Asking us if we had any questions, but in all honesty is was like listening to an episode of Charlie Brown. All we could hear is that annoying teacher "Wha WHa WHA". Our Doctors spoke very educated, soothing and far from annoying. But regardless what they were saying it still reverted to that teacher voices. I guess it was due to the anxiousness of the unknown. You're just thinking to yourself, "What is happening?"
Our updates on Natasha's progress and care.
Keeping friends and family informed on this rare cancer journey and sharing the grace that God is providing along the way.
Hi Everyone! We are so thankful for the outpouring of love and prayers for our family at this time. We wanted to develop this site for to inform everyone of Peyton's progress. We are overwhelmed with the amount of support we have received and we want to say thank you and keep the prayers coming!
Supporting Michelle as she heals her Heart and fights Breast Cancer
Megan is my 32 yr old wife who is fighting the battle of her life, as she sits and waits the next 80 days knowing she will going in for Open Heart Surgery #2, putting her life in the hands of Doctors, Nurses and Surgeons, Counting on them and god to bring her back to us and her beautiful almost 6yr old daughter Emmarie. Megan is tough, or atleast tries to pretend to be, but deep down she is terrified "how will i support the family if i cant work for 2 months" is constantly on her mind. We have saved as much as we can being the 2015 mid class working family but it is still not enough. If you can please find it in your heart to help Megan out and lift some of this weigh off our shoulders we will forever be grateful. Megan would never ask anyone for anything..........
Little guys has RMS, visit this site for updates and how you can help.
Elly and we are truly blessed with so many people who love and pray for her, especially at this challenging time. Thank you for all the phone calls, texts, emails, voice mails and of course visits here and offers of help. There is no way to fully express how much this means to us. I am sorry that we could not make individual calls to many of you but I'm sure you appreciate the emotional drain in each call. We are strong together as a family and your concern, support and prayers will get us through this and surely help us be strong for Elly I will continue to post to this site as we learn more to keep all of our family and friends updated. I am asking that you keep Elly in your thoughts and prayers as we help her heal and get back to her healthy self. She's a fighter and we are optimistic and confident that she will push through this. Much love and appreciation and Shabbat Shalom -Steve, Shari, Madison, Chandler, Lisa ,Joe, Jeremy and Casey
Welcome to our sight. My brother Rik has been diagnosed with end stage Renal Failure. He is facing dialysis and we are hoping to get him a kidney transplant. This site is about love,family, community and most of all faith..
A site to keep our community informed, and to provide an opportunity for people to offer messages of support.
Like the CANaries in the coal mine, our little girl has sensitive lungs from Cystic Fibrosis. We call her our little Callie-Canary, which has evolved to our CALLIE-CAN. Because? She CAN. Simply put. At 8 days old, our little Callie Rae was diagnosed with Cystic Fibrosis through the newborn screening process. We were devestated, terrified, and lost, but together we rallied as a family and picked ourselves up. We choose to look at this as an opportunity to appreciate each breath we are given because it truly is a gift. And now, we strive to give Callie's disease purpose and hope to inspire and help those around us. We know we can't change genetics, but we CAN certainly give it hell!
Updates for family and friends.
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Mike Volding's journey enduring a devastating diagnosis of stage 4 lung cancer. Inspiring with his unfailing optimism, Mike is an amazing and devoted father, husband, son, brother and friend to so many.
Sharing updates, thoughts and prayer requests as Ruth (surrounded by family and friends) faces her battle with Lymphoma.
Support and info for Terri Liestman
Updates on rehabilitation journey from spinal cord injury for Jon Miller
I am a relative of Conner and would like to track his progress over his rehabilitation.
For updates on the transplant so nice, we had to do it twice! I don't yet have a transplant date, but this site will get busier as we get closer to the action.
We want to use this site to keep all of our loved ones informed regarding Mike's medical updates and such. We are so grateful for all of your continued love and support. Thank you!
Our stay at Zale Lipshy and Carey's recovery updates.
Our beautiful girl was in a car accident and is currently in SICU-Surgical Intensive Care Unit at University of Utah Hospital in Salt Lake City, Utah.
Stage IV Colon Cancer
Please go to posthope.org/gracefisher
Jamie had emergency surgery November 23rd for acute internal bleeding as a result of a ruptured ovary. The pathology report indicated there was a Granulosa Cell tumor. (About 1% of ovarian cancers are ovarian stromal cell tumors. Types of malignant (cancerous) stromal tumors include granulosa cell tumors -the most common type). Based on the emergency uncontrolled nature of the surgery, it could also not be determined what ruptured -the ovary or tumor or both. In the weeks that followed two gynecological oncologists were consulted both in WI & AZ and it was recommend that based on tumor & rupture this is considered stage 1c ovarian cancer and chemo would be the next best course of action. Long term prognosis is very good for this type of tumor. Chemo (Carboplatin & Taxol) started February 12, 2015 at Aurora West Allis Medical Center. Moving forward there will be 5 more treatments. Each treatment is tentatively going to be 3 weeks apart.
This page is to provide you all with updates on my recent accident
Follow Mary's progress as she stands up to cancer, armed with faith and love. Please feel free to share prayers, words of encouragement, and pictures on this site. Let's show Mary how faithful and grateful we are!
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Keith's Brave Journey with ALS/Lou Gehrig's Disease
Road home and recovery updates......
Updates on Clare's battle against breast cancer
Danie Rae's adventure started on January 30th, 2015 at 11:55 pm. She entered this world weighing 1 pound 7 ounces and measuring 33 centimeters long. This blog will show her progress through her stay in the NICU and beyond.
This website is to keep friends and family up to date on Amy's Celebration of Life plans as they are made, and to be able to send love and support through messages, photos, and donations to Robert and Ava. Thank you all so much for your thoughts and prayers through this difficult time.
Sharing E's journey and accomplishments, check here for more of his story --->
A way to keep our family and friends up to date on Ben's medical journey for a diagnosis.
Charla Gets Well
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Welcome to the Team Teresa PostHope site. WE ARE ALL Team Teresa! Everyone who has prayed or taken care of Teresa and those she loves are part of Team Teresa. Teresa’s story: On Sunday, December 14, 2014 Teresa was a happy, healthy 43-year old mom singing Christmas carols at a nursing home with her church group in the Charlotte area. Just 18 hours later, she was put on life support as her lungs were failing due to the flu that brought with it a case of bacterial double pneumonia, which then spread. Teresa is a fighter and she is on her way back but, it will be a long, tough road for her, her husband Mark and their family. This page was created to support Teresa, Mark, Lani, John, the extended Henry/Sand families and each other over the coming months. We will provide updates on Teresa’s progress on this page and hope that you, in turn, will leave your words of encouragement and help us create a place of online encouragement for Teresa and Mark to use as they fight toward full recovery.
A place to send messages to Pat and for Pat to journal
This is where I am posting updates on Howard for friends and family.
Prayer and Support for TR
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