Thursday, April 9, 2009

NO CHEMO!!!


Megan had another MRI this week. Marion took her in on Tuesday then went back for more of the Cognitive Testing on Wednesday, and to meet with Megan's Dr's for a review of the MRI. They continue to do the Cognitive Testing and will monitor her scores. It seems that if there is something wrong it will show up in loss of memory and lack of function with her motor skills first. This will give them an indication something may be wrong and to jump into high gear. Megan did great, but was a little concerned because Marion and Megan stayed at Marcia's Tuesday night. They were up late, then had to get up early and be back at the hospital. She thought she may have scored a little lower just because she was tired. The MRI showed NO CHANGE!!! Yahooo!!! I didn't get to go so I did not get as much detail as I wanted, but bottom line is she did great. Radiation put the skids on things and we are believing for a total healing!!! The cavity where the tumor was had blood in it right after the surgery. Yesterday the results showed that the body had absorbed all the blood, and the cavity is now filled with spinal fluid. She has another MRI scheduled for 2 months down the road, and the testing will start all over. Dr. Lang took a look at the MRI and told Megan, "she is doing great!!" He is a great guy and gave Megan a hard time about her hair loss. She has a great relationship with Dr. Lang and likes him. Dr. Pudavalli said, "things look great, and its time for her to live again." He told Megan, "we have removed the tumor, treated the tumor, and now its time for her to go home, and be a mother to her children, and wife to her husband, and not worry about this thing any more. See you in two months!!" Thank God for His mighty hand, and for the Dr's he used to help Megan through this!! Thank all of you for praying. Please continue to pray for a total healing, and that her MRI in June looks even better.

Friday, March 20, 2009

Ring The Bell





Megan rang out last Friday to signify her last day of treatment. The bell is rung by all who finish radiation at MD Anderson in Richmond. On the bell there is an inscription that reads:

Ring This Bell
Three Times Well
It's Toll To Clearly Say

My Treatments Done
This Course is Run
And, I Am On My Way!!

It was met with huge fan fair, with about 20 of Megan's closest friends and family in the waiting area. When Megan went in for her treatment, there were about 6 of us in the room. When she came out they were calling for crowd control. She is truly done, and on her way!! She did not feel many side effects during the treatment but since has been experiencing some fatigue and nausea. We need to continue to pray for her total healing and strength.

Wednesday, March 11, 2009

This Storm Is Just A Walk In The Rain

This week Megan and I had a great trip to her treatment. We meet with the Dr. on Tuesdays, so I get to find out all the details. The Dr. and all the nurses said Megan is doing VERY VERY WELL!!! They all used very two or three times when they said how she was doing, and none of them heard the other. She has had NO! symptoms, other then the loss of a little hair. Her brother Jared said "Welcome to my world". Hair will grow back!!! Well for Megan anyway...sorry Jared... you can blame the Roberts side for that hair thing. We are very excited to hear the good news, and see that she is doing so well. She has experienced none of the side effects of getting sick and tired, weak, cranky.....wait....maybe that last one. She is the Megan we all know and love. She received a quilt from Aunt June with all of the names of people who have been on the blog writing to Megan. She took the names and embroidered them into the quilt. The quilt is a beautiful patch work and says "Megan we are pray for you" and all of your names are on it. Aunt June also sent a pen so people she meets on her journey can write on it. Lola is a friend that was going through the treatments at the same time as Megan. Lola writes " Think of this storm as only a walk in the rain". I love walking through the rain with my Megan!! This is the last week of her treatments. She will then have an MRI about every 8 weeks to keep an eye on things. They have a big bell in the waiting area that the people get to ring when they are done with there treatments. Megan rings the bell on Friday at about 11am. If you would like to be there you can call Marion and get info
(832-607-6937). Please keep praying for her. The prayers are working. She is doing VERY VERY WELL!!!

Thursday, February 26, 2009

They Have The Same Hair or Lack Of


This week was uneventful for grandpa. Nani watched the kids, and Grandma Elaine and I took Megan to her treatment. They met with the Dr. and all seems to be on track. Megan has started to lose some hair on the left side of her head. The Dr. said some of it might not come back, but we are not receiving that. We are praying it comes back the same if not thicker and curly. Megan is starting to feel a little bit of the fatigue that they say she would feel. We are praying for her to have strength, and keep her strong attitude. She met with Dr. Pudivalie yesterday. He ran the standard tests and said Megan looks great!!! He checked to see if there was any pressure behind her eyes, there was none. Her next MRI is on March 31st. They don't expect to see much change, but we are expecting the tumor to be gone. Lets keep praying for a total healing.

Better Look At Megan's Mask

Wednesday, February 18, 2009

All Is Well


Megan and I spent some time with the Dr. during her visit on Tuesday. The Dr. thought I was Megan's husband. This tells me two things. That I am still looking very young for my age. I told the Dr. when she was surprised that I was her father, "I am just very young looking and extremely handsome". She agreed!!! The second thing that it tells me is that the Dr. thinks Megan has some pretty low standards for men (sorry Felix). Oh well win some you lose some. Because I didn't have the girls with me this week, (Thanks Nani) I was able to push my way into all sorts of places. The young lady that helps Megan with her treatments was very surprised to see me walking in the back halls of the hospital like I owned the place. She was nice, but really did wonder who I thought I was just walking around the treatment center. After a little glad handing, and some Stork charm, she allowed me to go into the treatment vault. I am not sure that is what they call it, but that is a great name for it. Megan & I were taken down a long hall way into a room. They lay her on a table and fix a soft plastic fish net mask to her face, and then bolt it to a table. They then take a laser and align the radiation machine. They pressed a button and told me, "we need to leave now". As I continue to ask questions they cup their hands under my armpit and are pushing me back down the long hall. When I look up, I realize why they seem to be in such a hurry. The door at the end of the hallway is about a foot thick, and it's closing!! Once out of the room, I asked if I can stay and watch from the camera room. They politely, but firmly tell me NO!! "You must go back to the waiting area". A little more of the old Stork charm only produced another, but more stern NO!! "Now go so we can get our work done". I have a picture attached that shows the lasers used to aligning the machine as Megan is bolted to the table. It's not the best picture so I am working on getting a better photo. Please continue to pray for Megan, as the end of this week will mark the 1/2 way point of her treatment. The visit with the Dr. was fun. She asked Megan all kinds of questions, which Megan replied NO!! to most of them. Very few side effects if any have shown up. She has started to experience a little thinning of the hair, but that is about it. Please keep praying because it is working. I would also like you to pray for Brian O'Neill, and his wife Angie. They are friends through the blog & friends of my family. Brian is fighting a tumor also. You can visit his blog at aboneill.blogspot.com. Please do so and send his blog to all and anyone you know who will pray for him. We would like to have people all over the world pray for his total recovery.

Saturday, February 7, 2009

Should Not See Any Side Effects


This was Megan's first full week of treatments. The Dr. she met with on Tuesday said they don't expect to see much in the way of side effects from the radiation. Megan is young and has lots of energy. She is starting to feel a little bit of a burn on her scalp. She has been instructed to keep her head covered at all times when she is out side. They have also given her some cream to keep the scalp moist and help with the burn. She has not felt much in the way of fatigue, and the Dr.s don't expect her to. I think she looks great in a dew rag. The biker chick look does her well. Please continue to pray for Megan. I think I over heard the two little ones plotting to do grandpa harm next Tuesday. I am not sure because I can't understand a word they say. We are expecting God to do some great things. Please ask anyone you know to pray for her also.