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This is my beautiful daughter Paige. She is 5 yrs old and our whole lives changed on Sunday (July 3rd). She was brought to the ER with trouble breathing and some facial swelling. A chest x-ray showed a large mass in her chest. She was transported to Philly and more tests have been run. They are saying its Cancer. A biospy can not be done yet, so they started her on chemo. Please consider helping with the medical costs for my loving fun spirited little princess. She means the world to me.
July 12th, She was diagnosed with Tcell lymphoblastic lymphoma (non-hodgkins) and she will need 2.5 years of chemotherapy. This is going to be a very long road for her and for all of her family and friends. The doctors say this is very treatable and the mass has already started to skrink.
October 17th, Paige will be going for her PET scan to find out if the tumor has skrunk or it's gone! She is starting another phase of treatments.
We have been a frequent flyer at the hospital because her white counts are extremely low and she has had to get blood at least once a week, sometimes more. She has been a trooper through all of this and she has shown me how to be strong. She is the strongest little girl I know and I am so proud of her because she just keeps smiling through all of this.
Update: Dec. 2016. Paige came home briefly (3 days) from the hospital after a 2 month stay on the oncology floor. Her levels for her liver dropped and has been undergoing numerous tests and scans since Saturday, Dec. 3rd. She went in this time because she was lethargic and not eating. I was able to see her yesterday and put on some fun music for her. She got up and danced and moved around for 20 mins, which is great progress since Saturday. We were so overjoyed to see her up and moving around. Every little bit helps to get her back to our Paige. So we will take the 20 mins of joy and smiles.
Thank you all so much for the continued prayers and words of support as we battle with Paige. You have no idea how much all the support means to us.
July 12th, She was diagnosed with Tcell lymphoblastic lymphoma (non-hodgkins) and she will need 2.5 years of chemotherapy. This is going to be a very long road for her and for all of her family and friends. The doctors say this is very treatable and the mass has already started to skrink.
October 17th, Paige will be going for her PET scan to find out if the tumor has skrunk or it's gone! She is starting another phase of treatments.
We have been a frequent flyer at the hospital because her white counts are extremely low and she has had to get blood at least once a week, sometimes more. She has been a trooper through all of this and she has shown me how to be strong. She is the strongest little girl I know and I am so proud of her because she just keeps smiling through all of this.
Update: Dec. 2016. Paige came home briefly (3 days) from the hospital after a 2 month stay on the oncology floor. Her levels for her liver dropped and has been undergoing numerous tests and scans since Saturday, Dec. 3rd. She went in this time because she was lethargic and not eating. I was able to see her yesterday and put on some fun music for her. She got up and danced and moved around for 20 mins, which is great progress since Saturday. We were so overjoyed to see her up and moving around. Every little bit helps to get her back to our Paige. So we will take the 20 mins of joy and smiles.
Thank you all so much for the continued prayers and words of support as we battle with Paige. You have no idea how much all the support means to us.