I am in need for tires for my old truck so I can feel going back an forth to the doctor Thanks GOD bless
A place for updates, prayer requests, communication, and encouragement for the Lawson family. If you would like to support the Lawson family with meals, practical tasks, etc., please email firstname.lastname@example.org.
as an infamously horrible communicator, to keep the loved ones updated
Keep up to date and provide your love and support on Jennifer's journey to becoming cancer free.
Sharing updates with friends and family on how Troy is doing.
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Out of suffering have emerged the strongest souls; the most massive characters are seared with scars. Khalil Gibran
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This group is for us to keep you all updated on what's going on with Beth's treatment, and for you to post encouraging comments, articles, scriptures, etc. Thanks so much for your support!
Testicular Cancer -- The Parental Journey
This site will be updates with the progress and status of Jen's health since her motorcycle accident on Monday, May 4, 2015.
This is a journal of my battle with testicular cancer.
Follow the Branchini Family as Reg begins his third fight against brain cancer (glioblastoma multiforme)
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I was diagnosed on April 22 2015 with Non-Hodgkins Lymphoma. This site is dedicated to my story so that my family and friends can follow my progress to success.
Come to this site to see periodic updates from Debbie and Rich on Debbie's status.
This site honors, Frances Ann Shea, who continues to delight the world with her charm, wit and grace. We hope her family and friends will feel free to post thoughts, feelings, photos and memories.
Deb's journey with having two broken wrists
See updates about Hiley's journey regarding her needed heart transplant.
Follow me on my journey to choose life while facing Metastatic Breast Cancer
Sharing information about Susan's fight against amyloisosis starting with her stem cell transplant.
Follow Devon's progress, read her posts and watch her videos
Here we will keep you updated with the current status of Genevieve's health. Please feel free to post your stories, love, and support for the woman that has made such a wonderful impact on so many lives. Let's all keep her in our prayers and in our hearts.
Dear friends and family, Thank you for your ongoing support. This website serves two purposes. On the one hand, it allows us to let you know about changes in Laurie's status. Alternatively, it lets us ask for help in a more organized way. Hopefully there will be long periods of inactivity, but we'll try to at least provide periodic updates. In all likelihood, the times when we need help the most will be when we are least accessible, so during those moments you will likely see posts from other family members keeping you informed. Thank you again for your love and compassion as we progress along this path. -Jeff
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Hi Family and Friends, As many of you have heard, Kristine was diagnosed with ALL (acute lymphocytic leukemia) on April 1st. We have been overwhelmed by all the love and support. We will be using this site to post updates as we journey this road with God. He is our Healer.
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A private place for updates on Pete, as well as, a place to post supportive messages.
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 what this mean for me.. for us. I d[...]
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.