PrayfortheGantgirls: March 2022

Well, yesterday Tuesday March 6 we met with another neurologist, this time at Memorial Hermann Children’s Hospital. Don’t want to get overjoyed with her being so “observant and knowledgable” to Olivia but I have to say I went in with an open mind and an open heart….I thought. We met with her for RO housing – https://www.hulkshare.com/jaguarfloor9, a little over two hours. She read through all the previous reports, looked over all the scans, ultrasounds, MRI’s and lab reports. While discussing Olivia’s daily behaviours, problems and concerns, she showed me all the MRI’s. In between all of our brains, there is a thick membrane lining housing all of the nerves that connects our right side of the brain to the left. It allows all the nerves to send signals back and forth properly, keeps everything in tact. Well on the first MRI back in July of 2011, the radiologist noticed that the membrane was thin. He quoted ” concerned about the thinning membrane lining the corpus luteum”……..was that EVER discussed when neurologist got the report, NO! OK am I angry, thats an understatement. Then the last MRI that we had on February 24, 2012, reported that there was no lining……OK am I pissed off now, NO I have surpassed that emotion. I told her am I supposed to be glad you found this! Why can’t I just find out the first time what in the hell is wrong with my child….Im sorry I am so angry, frustrated, full of emotions that I’ve never even had before but you are talking about something that we could have known about a year ago. Not that anything could have fixed it as the conversation went on. As her explanations of the days to come continued but still. Why go to medical school, why take an oath, why have a practice if you’re not gonna follow what you promised. WHOA!! I just put my foot in my mouth. I promised myself, I promised God that no matter what came out of the doctors mouth whether it was what I wanted to hear or not, I was going to accept the answer, accept the outcome and say what do I do next….You know it really is hard to do what you set out in your mind to do, or what others recommend you do when you’re faced with your child suffering, living a “not so normal” life and feeling absolutely GUILTY over the fact that maybe you should have sought an outside opinion sooner,maybe you should have fought harder to begin with. Maybe so, or maybe I should have shut up along time ago and listened to God tell me you are the mom and I am the healer. You don’t have the letters behind your name that say M.D. you dont have the nail scarred hands to prove you CAN do it all, you just have my child to care for, my child to teach and raise and my child that I can heal on Earth or in Heaven….I am so humbled when the good Lord brings me to my knees once again because it truly lets me know the power of His love, His forgiveness and of His presence in my everyday life.

Needless to say, by the end of the visit with the doctor, I was pleased that we met with her, upset over some of the news but accepting of the fact that we have plans, plans in place for the days to come. We have a strategy of how things will be with Olivia and how we are going to deal with her and the best of all, we actually have a follow-up appointment with her after all the future tests that are ordered will be done. Olivia will have an MRI of the neck and lower spine, followed by a spinal tap to remove excess fluid so that the fluid from the brain can drain down. She is going to start steroids an on/off regimen to help reduce swelling and hope and pray that the brain begins to breathe and realizes there is space and it can begin to grow. Next she is going to start her on seizure meds for a trial period of 30 days to see if there is any change in behavior. To see if she begins to sleep at night, has less screaming fits. She is also scheduling a hearing test to see if there is any damage since the tumor is on the paratiod gland which houses the nerves. She knows she hears us but the question is how well..The best news was all these tests will be done within the next few weeks and ALL results will be in when we go to our follow-up visit. That was an answered prayer that wasn;t even prayed for….at least by me, maybe one of my wonderful prayer warriors asked for that and if so I am eternally grateful!!

As far as dealling with Olivia, she is going to need to continue her therapies, she is going to need the extra pushes to grasp concepts, commands and everyday life as opposed to others…. If you have just about any concerns with regards to in which as well as how to make use of Reverse Osmosis Membrane (Www.Blurb.Com), you can contact us at the page. but we can handle it, we can handle anything….thanks to a very dear friend who helped me realize that it’s going to be hard but not impossible. Olivia has had an interview at a very good school that deals with children with autism. Neurological disorders in hopes that this might be the place for her. We have also had an interview with some therapists that can come into the home. Do the same treatments that this school would do. We are just waiting to hear back from both places and then praying that what God wants for Olivia that we will be open to and accept.

Please continue to pray for Olivia. All of this has been very difficult on her and on top of all the usual things we are currently going downtown to Texas Children’s daily for whirlpool treatments for her excema and this will continue for quite some time. That is hard but she is doing good on the treatments. Seems to fight a little less each day. Please continue to pray for sam and hannah as well. This has been hard on them with having to be at the hospital lots more than normal, but as always they seem to adjust and it becomes a routine thats not even questioned. As always, thank you so much to all of you who pray for my precious babies for their comfort, for their healing, for their peace. Thanks to all the many wonderful friend who have been their to love on my babies, give them a little joy and give me a little help even if it is in the surroundings of Texas Children’s…..we DEFINITELY have a wonderful church family, wonderful family and friends. Thanks to all who pass along this blog and share and ask for prayers, it’s greatly appreciated. You all mean so much to me, those who are my nearest and dearest, those who are aquaintances and those of whom I have never met, you mean the world to me and my family for taking the time to read, pass along and pray. I truly believe God hears all our prayers and I know He has already answered I just have to be patient and trust and have faith in Him.

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