Sunday, August 1, 2010
My Warrior Princess
She's not even 4 yet, but she has endured 2 painful air enemas (no sedation or pain relief because of the danger of intestine perforation), one major abdominal surgery, IV lines coming out from left hand, right hand, left chest through her implanted port, lots of repeated blood tests, finger pricks, lumbar punctures...chemotherapy. after each tear has been shed, she smiles a ray of sunshine and dances to praise and worship songs. She reminds me that God has already healed her. She tells me she's not scared as God is with her. I am scared. I am scared witless. I am scared I might lose my little girl. She is my miracle baby, the one that almost didn't happen. What if God loaned her to me for a fleeting moment? Research shows that 85% of lymphoma patients recover. What about the 15%? So far, we keep falling into the minority percentage. We are the 3% chance that got cancer. I'm falling fast but grasping. reaching for a miracle. She tells me thousands are praying for her. I hope God hears the prayers of the faithful thousands.
Friday, July 30, 2010
A deserved break
"We are going home after dinner! Yay! I think we all need a break from hospital and needles."
Thursday, July 29, 2010
Maeve is getting weak
"Maeve is starting to feel weak and she does not want to walk at all. Pray that she regains some strength in her legs and that the leg cramps will go away. She is also starting to ask why the other kids here have no hair. Do not know how to tell her. Pray for wisdom and that she will not lose her self esteem when it happens."
Wednesday, July 28, 2010
A mother's heartache
"Yesterday was very stressful involving lots of needles and pain. It was very hard watching her go through it all and not understand why I let them hurt her. Pray that today will be event free and we get to just rest. Thank God the side effects have been minimal so far. Except for the mood swings. I know this is because a whole army is praying for Maeve."
Yes, indeed a whole army is praying for Maeve and the Low family. Let's continue to intercede for them!
Tuesday, July 27, 2010
The Low family is sick!
"Please pray for my family. Mum and dad are sick. Bernard and Paige are sick. I am the only one left standing. Pray all will recover before we go back this weekend. Maeve cannot afford to catch it with her very low immune system."
Monday, July 26, 2010
Good news!
Just received a sms from Jo:
"Results show the cancer did not spread to bone marrow or brain. Thank God ! Start chemo later in the evening. Pray for minimal or no side effects and Maeve will be comforted. She is very upset to be in the hospital again."
"Results show the cancer did not spread to bone marrow or brain. Thank God ! Start chemo later in the evening. Pray for minimal or no side effects and Maeve will be comforted. She is very upset to be in the hospital again."
First cycle of chemotherapy
Maeve is going for her first full dose of chemotherapy on Monday (26/07). It will be a 5 days therapy with a 1 day of hydration. Hydration has the purpose of flushing out the toxin and dead cancer cells through urination. During the chemotherapy, different people will have different side effects. Some of them are mood change, constipation, vomit and hair loss. Please pray that Maeve will have minimal side effects during this cycle of chemotherapy.
Although the lymphoma is currently isolated, it has the chance of spreading to other parts of Maeve's body. Hence, she is given injection periodically to protect the cancer from spreading to her brain. As this injection is a painful process, Maeve has to be sedated every time she has the injection.
Maeve did a "baby dose" of chemotherapy while she was in the hospital. It was to test whether the therapy is effective. When it was tested the last time, it showed very positive and encouraging result. So please pray that this full dose of chemotherapy will be as effective.
Someone said doing the chemotherapy is like running a marathon. It is a long process that needs a lot of stamina and determination. The Low family is going for their first lap of marathon. They need our prayers, support and encouragement.
So remember them while you start your day this week.
Although the lymphoma is currently isolated, it has the chance of spreading to other parts of Maeve's body. Hence, she is given injection periodically to protect the cancer from spreading to her brain. As this injection is a painful process, Maeve has to be sedated every time she has the injection.
Maeve did a "baby dose" of chemotherapy while she was in the hospital. It was to test whether the therapy is effective. When it was tested the last time, it showed very positive and encouraging result. So please pray that this full dose of chemotherapy will be as effective.
Someone said doing the chemotherapy is like running a marathon. It is a long process that needs a lot of stamina and determination. The Low family is going for their first lap of marathon. They need our prayers, support and encouragement.
So remember them while you start your day this week.
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