Farm Journal

Today, at sundown, we will be entering into the new Biblical year. The Barley was found to be at the correct state of ripeness (Aviv) and the moon could not be seen last night due to it’s position in the sky in Israel, so the new moon has been differed to the 30th day after the past new moon.

In 14 days we will be celebrating Passover and then Unleavened Bread. We look forward to the Spring Feasts and remember the coming of our Messiah Yeshua (Jesus) to take the place of the lamb of Passover that was slain for our redemption.

We will be spring cleaning until Passover to remove the leaven from our home, our life, our heart. The most important thing is to look for sin in our heart and things in our life that may cause us to sin. This year the Father has put on my heart to be careful of mixing. This is a primary theme throughout the Word. When the people made the golden calf while Moses was on the mountain, they said that there was a Holy day and that they would worship the Creator G-d with the golden calf they built. G-d was furious! He does not want us to worship him the way that the pagans worship their gods. Over and over he reminds us not to mix or mingle. We will be cleaning out things that may be mixing in our home and our lifestyle.

There is controversy about which year it will be, but Michael Rood suggests that this is the year 6010. I think his info is accurate and important so check out his sight.

Happy New Year!

Whew! I’m exhausted… But we are home! Yay! My own bed felt so comfortable after sleeping in chairs, hospital rooms and hotel beds!

So,  Tuesday morning ICU has Shelly up in the chair at 4 am and by 7 we’re headin’ to the MRI and then to the regular room. The Docs came in and said everything looked great and asked Shelly if she wanted to go home today! (I’m a little stressed by now and wonder if we can’t wait til Wednesday?) But, alas, the docs had different ideas! Shelly walked around the ward a couple times and took a couple catnaps, ate breakfast and lunch and sat in her chair until the Surgeon came by to take the central line out. They finished getting everything done and by 5pm we were heading to the Ronald McDonald house to clean up and load up. We ate dinner there and started for home about 6:30. We had to get some prescriptions filled on the way home and by the time we got to Huntsville we ended up going to 3 pharmacies to get them. Then we headed home.

Shelly’s night went well, she was up early this morning and came in to bed with me for a catnap. She has been up today helping a bit and ate a good breakfast. She is resting now and the swelling has gone down to just minimal. She gets cold easy, probably due to no hair, and tires out quick, but that will get better in a few days. She will have her staples out a week from Thursday!

Our Thanksgiving and prayers go first to the Heavenly Father who has His hand in all we do and has made miracles as we walked this difficult path. And second to each of you who have walked with us, holding us up in prayer as we have made tough decisions and faced fearful situations. Special thanks and blessings to those of you who have helped us through with encouragement and physical and financial aid, we could not have done this without your obedience to the Father. Our sincerest gratitude for your obedience.

We pray now for each of you that Yahweh bless and keep you, Yahweh make his face shine upon you and be gracious unto you, and Yahweh turn His face toward you and give you Shalom. Amen.

Yahweh is amazing!

If you have been praying for Shelly, we would love for you to send her a post card… she has people praying for her all over the world and we thought she would really enjoy getting a post card from each of you with your location on the picture. It would encourage her during the recovery time and give her something to look forward to. We want to make a collage for her room to reminder her how Yahweh uses His people to pray and stand in the gap. If you can send her just a simple post card with a word of encouragement we would appreciate it!

Send your postcard to:

Shelly Berry
PO Box 8391
Huntsville, AL 35808

Ok, So Shelly is out of surgery and in ICU until tomorrow. Lots has happened today. This morning the neurologist did a test to find the good areas around the bad area of the brain… wanting to make sure they don’t disturb the good areas when they to the resection (removal of the area of brain that is causing the seizures.) The test should take about 2 hours. So they get started and the nurse decides that she needs to start the plasma that was ordered for an hour earlier right when the doc is trying to set up for the test.. hmmm. So the doc stops the test and waits until she is done. Then the blood pressure machine starts beeping because she didn’t turn it off. Then the nurse call button starts calling the nurse (but no one is pushing the button). Hmmmm. Then the remote control (connected to the call button) starts changing the channel all by itself. Then the plasma finishes and the machine starts beeping… then Shelly has to go to the bathroom and we finally take a break…. start back up with test and the doc gets an emergency page. Then a student calls him and he goes out to meet her so she can find him so she can observe. 3 hours later we finally finish the testing! The enemy was really in the way.

The test results are in and the brain mapping is done and they come to talk to me. The neurologist that was doing the language analysis said that her language area had remapped to another area of the brain (same as the physical when we did the MEG last spring). The seizure data showed that there is a very precise area in the brain that is causing the seizures. They told me this info at 1:30 today and said they would be taking her to surgery as soon as the OR opened up (at 3:30).  I asked one of the neurologists if he were to put a percentage on a cure from this surgery for Shelly what would it be… he told me better than 75%! Yahweh is Great!

Shelly’s surgery went well. She has a really bad headache. Satch is staying with her tonight in ICU. Tomorrow they want her up and moving early, 6 AM in the chair. Her eyes will be swollen for a while and there is a lot of bruising from surgery, but she has come through with flying colors. They did an EEG after her surgery and she had no more seizure spikes!

We should be going home on Wednesday and will have a couple weeks before the staples come out and 6 weeks before she can go back to full normal activity.

We will be keeping a low profile for the next couple weeks while she recuperates. Keep us in prayer (so we don’t go stir crazy!) and in a few weeks we would love to have company!

Hello all,

Shelly went into surgery at 3:30 pm today and is still in surgery. The Docs were able to compile the data and map her procedure earlier. They did a language evaluation and test to see where her language center was in the area with the electrodes. Once that was completed, they took her to surgery… I will let everyone know how things go tonight.

Thank you for your continued prayers.

This morning they moved Shelly from the NICU to the Seizure monitoring unit. She hadn’t had any seizures through the night. We were hopeful today that seizures would come and they did. She began having mild seizure activity that was only detectable by the internal monitor, but they were not showing up in her body. We had to stay with her to monitor when the seizures showed in her body. Well, my dad and brother had made it to visit and get Satch’s truck home and my mom and I saw an opportunity to take a break and we walked down to the street. My phone rang and it was my brother telling me that Shelly had gone into seizure. We hurried back upstairs.

They had given her 2 mg of ativan to stop the seizure by the time we arrived. The seizure didn’t stop, so they gave her 2 more. The seizure didn’t stop. The neurologist asked me how long it takes for her to come out of seizure. I told him when you give her enough meds! She was having a generalized tonic clonic that went static (for those of you who know seizure terminology.) The doc was really concerned and gave her another 2 mg of ativan, it was 45 minutes into the seizure. Still it didn’t stop, so he asked me how much we give her. I told him 10 mg of diastat at a time up to 20 mg. He called the nurse for the ambu bag and we cleared the room (except for mom and me.)  They gave her another 2 mg of ativan and loaded her with dilantin. She finally started showing signs of the seizure activity slowing down. He asked if she had ever had a static seizure before and I explained that for the last several years all of her seizures were static. They were very concerned and sent her back to the NICU.

She is doing better tonight. She is sleeping mostly and Satch is staying with her in the NICU.

The docs have decided that they have enough info for surgery and that they don’t want to see her go into stasis again (prolonged seizure.) They have her back on her meds and it seems that they may do the surgery Monday afternoon. We will know better tomorrow.  Yahweh has blessed.

Shelly got out of surgery at 11:30 and is doing well. The mesh is in place and she is hooked to the monitor. She has a headache and sore throat from the vent tube. When she was finally hungry, they brought her a big piece of chocolate cake which she quickly devoured! Tonight she will be in the NICU (Neuro-surgical ICU) to be monitored. We found favor with the neurosurgeon and got special permission to stay with her in the NICU. Tomorrow they will move her to the seizure monitoring unit. Now we wait. They want to monitor the beginning of her seizures, a minimum of 3, so it may take a little time to get 3 or more separate incidences. We are praying they come quickly.

We are not getting much sleep, so please pray also for us to get restful sleep.

More updates to come.

Hey to all!

We came down to B-ham on Wed… The Ronald McDonald house did not have an opening, so it was off to the Motel (not much sleep there, it was right next to the freeway!)

Then Satch’s truck broke down on the way down here last night and I had to wake up and drive to get him (hasatan is still alive and well and bothering people on planet Earth!)

This morning we visited with the doc and anesthesiologist and did Shelly’s blood work. She cried, but was brave and all was well. She still wants to go home!

Satch had the truck towed to the nearest exit and My dad and Brother will bring my mom’s car (so Satch can get home on Sunday) and their truck and car hauler down on Saturday. They will visit and then pick up Satch’s truck on the way home.

This afternoon we got into the Ronald McDonald house (thank goodness, ’cause now we have to repair a truck!) and went to get some groceries. Money doesn’t go as far here as it does at home! $250 of groceries was very little! But we found out that they will feed us here at the House breakfast and dinner, so we just needed lunch stuff.

We have to be at the hospital tomorrow morning at 5AM so it will be an early night tonight.

Blessings to all who are praying for us!

Christie

Shelly is nervous and wishing it was all over…

The Father has truly stepped in and provided for our finances! Baruch HaShem Yahweh! Thank you to everyone that has helped us! May Yahweh Bless you and Keep you!

Hello to all,
On Jan 20th Shelly will be going in for brain surgery. Please pray God’s hand in all that happens. I will update our blog from the hospital as I can.

The hotel will run us $45/night (plus tax) and we expect to be there for 2 weeks. Currently there is a waiting list at the Ronald McDonald house of 20 families. You can make donations via paypal to clberryr@gmail.com. Thank you!

Please share this blog site with all who will pray for us during this difficult time. You can read Shelly’s Story here.

Thank you and Blessings,
Richard and Christie Berry