Showing posts with label summer. Show all posts
Showing posts with label summer. Show all posts

Thursday, May 9, 2019

Half Way There!!

The End of Summer!!!

July came and there was no sign of Nikole.  Monday morning I helped Rhett called the Social Security office to set up an appointment that way he can apply for SSI.  Nikole was finally here!!  I was happy to see her and I hope she was happy to see us and be home.  Wednesday after the 4th of July Nikole, Rhett and I went down to the the West Office Building and the Church Office Building to meet the people there to see where he would like to serve his mission.  He decided to serve in the West Office Building and at home on the Virtual Records Operation Center.  The next day I took Nikole to urology for an appointment.  She was not happy about that, and we also found out that he had a bladder infection. She was put on medication and told that they would like to run more test later this month.  I took her and Rhett to the DMV for a eye exam and for Nikole to see if she can get her permit.  The next day I took Dylan to scout camp.  It was day camp and he had a blast even though it was dusty and he didn't like that, but everything else besides losing one hearing aid was great!  Since it was up a canyon I had no cell service so as soon as we left the canyon and jumped on the freeway, I instantly starting getting messages and voicemail's.  Apparently Nikole was sick and throwing up all day.  So I called the doctor as I was headed home to get her an appointment and the soonest that I could get her in was 4:20pm.  When I arrived home Nikole was laying there looking really sick and of course Rhett was sitting there really worried, Gavin was not very fazed.  I talked to Nikole while she was laying there, thankfully not vomiting.  She had emptied her stomach earlier when I was at scout camp with Dylan.  When we got to the doctor she just laid there.  The doctor was stumped so they drew labs to see what was going on with her.  Of course there was infection but we were not sure where the infection was coming from.  I let them know that we had just been to urology and that she has a bladder infection that she is taking antibiotics for.  The decided to give her a shot of antibiotics and put her in more than what she was already taking.  Sadly I missed my friends surprise party the next day since Nikole was sick, but I am grateful for Nikole and what she brings to our family so it was not hard to be with her.  The doctor called me Saturday to check on Nikole since we were at the doctor's office until after 6 pm, I told him that nothing had changed very much.  The doctor guessed that she had a kidney infection.  By Monday the next week she was doing better thankfully.She was still on heavy duty antibiotics, but at least she was not vomiting all over and sick as can be.  I am grateful that she was doing better since she was leaving for Trek on Wednesday morning.  She was able to make sure that she had everything in her bucket and all her camp gear ready by Tuesday night, since we needed to drop it off at 6 pm Tuesday night.  Wednesday morning she was leaving and had to be at the church to leave at 6:30 am.  Do they realize they are taking teenagers?  Teenagers do not wake up that early on their own unless it is because of bribery.  The same morning she was leaving for Trek Rhett had a driving test at the DMV in order to get his licence.  Thankfully I could go with Nikole because daddy was able to take Rhett down to the DMV.  I was at the church waiting for the buses to leave before I left.  As soon as the buses left I soon left and started the drive home.  Little did I know that the bus that Nikole would get on broke down on the side of the rode right before the freeway.  I was the first person to come across the group and called for help.  Soon the stake people who were in a car pulled up behind the bus.  They had everyone get off the bus and then empty it since the bus people were sending a new bus and taking the broken bus to the shop to be fixed.  I hung out with them until the new bus came and they reloaded the new bus and drove away.  It has been a long summer without her around.  I did let the nurse who was on Trek know her medical problems that way I knew someone would know her just in case something happened.  The Saturday that Nikole came back from Trek we went to a 5k and then a car show for Angel's Hands Foundation.  The boys were able to pick out their favorite car to give a trophy to, and they all compromised and picked the yellow Camaro that looked just like bumble bee from the transformers.  As we were leaving we hurried to the stake building to pick up Nikole.  She was the last to be picked up.  I felt bad that we were not there when the buses came back.  I know I would have been there if I had been by myself, but because I had the boys and their daddy with me there was no way to get there when the buses arrived.  I was happy to see my baby girl.  While see was gone we found that my dad had a blood clot in his corardid artery.  The doctor said that he thinks that the artery is blocked possibly up to 95%, so he needs surgery to clear that clot out.  The Monday after Nikole got back my dad went in to have a stress test done on his heart to make sure he is healthy enough to have surgery, since he is now scheduled for surgery on the 25th of July.  This was really hard for my mom and I kept having to tell her that it will be ok and things will work out.  We were also having washing machine and dryer issues that we had someone out to try to fix them before my sister came out from New Jersey.   The day after my dad had his stress test and finding out that he was healthy enough to have surgery, Nikole went in for her follow up appointment to the sleep clinic and we reviewed the sleep study with the doctor.  She was going to have surgery in 2 weeks. HAHAHA!  Rhett and Nikole had a visit to the orthodontist the following day  to get the bands changed and to check retainers.  Rhett and Dylan had a follow up at Shriner's on Thursday.  They are just being monitored and watched there.  Friday Nikole had a VCUG for her bladder.  She did not like it at all, but we found out that there is no reflex into her kidneys!  YAY!!!  I was happy to know there is not that medical problem on top of everything else that I need to deal with.  
It was also Gavin's birthday!  I cannot believe that he is 12 years old!  We had a cake and ice cream and a little party with cousins since they are not normally here.  Gavin you are a light in our family and you shine so brightly.  The Lord knew I needed you, I love you dearly and I hope you will always know how much you mean to me.
My dad had his surgery on the 25th of July and he did really well. The doctor wanted to keep him over night to just make sure things are going good still even after a 24 hour period.  We did find out that his artery was blocked at least 95%!  Oh my goodness!  The blood clot did not get lose and they were able to get it all out.  If it had gotten loose he would have had a stroke or even died.  We are blessed that he is still here alive a kicking.  Gavin had a well child the Wednesday after his birthday. Of course he needed shots to get ready for 7th grade, but other than that he is really healthy psychically.  He does need to see someone for these moods and attention problems that we are running into.  The boys had a wheelchair appointment up at Shriner's after Gavin's well child visit.  Their chairs are well and we made sure they fixed the problems that we had with weight distribution.  Nikole had a follow up appointment with urology the following day.  We officially got the report that she does not have reflex in her bladder (even though I already knew that from looking at the screen and watching her test).  The following morning before our trip to Idaho, Rhett had an appointment for SSI.  We went down there and was there for at least 2 hours going over all medical history and income for Rhett which is la lot of paper work.  When we were finished we got home and loaded the car with all of our stuff and daddy's stuff and caravan-ed to Idaho.  If course it is about a 3 hour drive.  I was exhausted, so I didn't drive, daddy drove.  We had a great weekend with family and I am grateful that I have family who loves me. Sunday we drove back and it was back to crazy with appointments starting Monday.  Both Gavin and Nikole had an appointment with the psychologist.  We decided that Gavin is improving with the mood medication and neither one of them is wanting to take any other medication right now, and with that July was over!  With July ending our pediatrician also retired.  We are so sad to see him leave and have to find a new doctor for the kids.  Thankfully he recommended a doctor for us.  We will miss you Dr. Gardiner!!!

August first my dad had his first appointment after surgery with his doctor.  Just to let them know he was still alive and to just have a follow up.  Wednesday August 2nd Nikole was schedule to have surgery to get her tonsils out.  She was not happy.  So upset.  I took a picture of her where she looks just like her little cousin who I snapped a picture of her when she was really upset.  Surgery went well, even though afterwards she did try desatting (oxygen levels dropping) while she slept due to swelling.  While she was recovering daddy went and got Rhett for an eye appointment. After he was finished we were able to take Nikole home.  As she slept I found out that a friend's son got hit by a car in Hawaii.  He was in ICU and should have died.  As a parent who is always in the hospital with children I know how hard it is having kids in the hospital with other kids at home and knowing that you cannot do anything for your child, other than pray, talk, and hope that the Lord will give you the answers that you want.  When Nikole woke up from sleeping I let her know what had happened to this little boy who is barely younger than Gavin, her heart went out to him and she was determined to send him something to let him know that she was thinking of him.  I reached out to my friends to see how they were doing.  I know from a parent's perspective how gut wrenching trauma can be, and I know my friends have suffered before loosing their youngest son to whooping cough, they have also lost their foster children back to the birth mother.  My heart really goes out to them, that is a lot of stuff to go through.  It made me happy to know that my daughter was thinking of others even when she was hurting and sore, but she said that she has nothing to complain about since she knew that he was hurting much more than her.  Her tender heart, and her creative mind drew him a picture that she was hoping that he would really love since she loves art.  Friday we meaning Rhett, daddy and I met with a lawyer to go over things for a POLST (physician order for life sustaining treatment) since we had gotten help in May for advanced directives and a medical proxy.  We needed to add to it what did Rhett want before he started his mission.  All that paperwork back in May was still good, but just in case the mission people wanted to know what they are allowed to do and not do in an emergency.  Do you have any idea how hard it is explaining to a 18 year old what a DNR is?  It is no walk in the park, and later that day I just cried.  The next day we met with the stake president and Rhett was set apart as a missionary.  I cried since I was so happy that he could experience this for himself now.  Monday we had a new kitchen sink installed for my parents.  Their was was leaking and was making life a little difficult, but now has a new one.  The following day I took oxygen down to the Global Service Center where Rhett would be serving his mission from, and talked to them about where it is going to be and how to take care of it.  Thankfully we also had all the paperwork that they could get a copy of and the sweet couple that are his "supervisors" know medical stuff.  She was a nurse when she worked before her mission.  The next day was registration for Nikole in High School and Gavin in Jr High School.  I went to work after getting them into school.  The next day Gavin had a play date with his cousin. My parents had a MS thing Thursday and Friday afternoons.  I took my dad to his by-pap appointment that following Tuesday.  Gavin and Nikole were invited to go on a boating activity that afternoon on Tuesday.  School is going to start and I need to make sure I have everything not crazy. Wednesday Rhett had a Orthodontist appointment and while we were at the hospital we dropped off the form for the cardiologist to sign for the driver's license division.  I also went to a meeting about helping those that have neurological issues to see what can help without medication.  Of course my kids were not happy to hear what I found out.  Rhett had to see the doctor on Thursday since he was getting sick and having issues.  Dylan had an eye doctor appointment Friday, and of course his glasses prescription has changed, which means new glasses.  He has refused to get new frames and glasses for a year.  We will see what we can do.  I had an opportunity to go with my sister and mother to a women's retreat Friday afternoon through Saturday afternoon.  It was great to get away and have time just for me.  It was awesome spending time with my mom and my sister without any kids to stress over.  When we got back in town I took the kids down to OBT to see a play Saturday night.  We had a lot of fun and the play was so funny.  That was the last hurrah before school started.  School started Monday for everyone.  What a crazy day that was.  It was good to get into the swing of things with school for everyone. After making it through that first week of school we had the opportunity to go to Cowabunga Bay with Mascot Miracle Foundation.  We had a lot of fun playing in the water and enjoying the end of summer while we had a chance and before anyone is really sick.  The last Wednesday of the month Nikole finally met the allergist and had a scratch test to see what she is allergic to, and she was not happy to find out that she is allergic to most things.  Including cats, and she was so not happy to know that since she loves animals. With that summer was over and it was now fall as September appeared.

We started the month out with a cardiology visit for Dylan and Rhett.  Both of them are doing as good as expected and thankfully the doctor could not see the hypertension we all know they have which means their hypertension is not getting worse right now.  Rhett's hypertension was still really high and they talked about exercise that they wanted him to try and we told them what the physical therapist said that after 30 second his pressure increases. So they are still try to figure out how to get him moving to help his weight but knows that if he does too much his blood pressure will be too high which is very dangerous.  Thankfully they are following Dylan and watching him, and there has been not a lot of change yet. The day after the cardiologist Dylan had his IEP and it is a struggle as the school isn't excited to pay for an interpreter.  He still has an interpreter and he is still in a mainstream class, but he is struggling since he was so far behind to begin with.  Now we are working on forming letters, multiplication facts, and comprehension when reading.  The school wants him to be more proactive asking for his interpreter when kids do not understand him or when the teacher is teaching, they want him to be using the interpreter to understand what is going on.  I am frustrated since I know many Jr high kids that do not even ask for help or advocate for themselves.  He is only in 4th grade!  Geez this is only the second year that he has been in a "hearing" school.  Because he is hard of hearing he can hear somethings but trying to communicate back is still hard for him, and there have been many nights he is crying telling me that his mind is blank and he cannot think. :(  My poor baby!  Thursday both Rhett and Dylan had an appointment with the orthodontist and we are just watching to see how Dylan is doing knowing he cannot bite very well and of course Rhett is almost out of braces.  He is so excited!!  They are still waiting to see how Dylan's mouth will form and what will need to happen before they do anything.  Nikole had a follow up with the ENT a week later since she needed to have a follow up after surgery.  She has recovered well and everything is good.  The following day Rhett and Dylan had a pulmonary appointment, where they again had a PFT and of course it dropped again.  They really want to find out if Dylan's lung function is truly dropping or if it is a fluke and it was just that day so they want Rhett and Dylan to return in 3 months to find out if they are still dropping.  On those days seeing the results up front and in your face are really hard.  Yes I know they are not good and I know that Rhett is declining and now Dylan is but I never know how bad they really are until those doctor appointments.  I usually end up crying and having a moment because it is hard and it is hard often.  I usually do not show it since I have to keep going.  I also have so many responsibilities that I need to do that I cannot just cry for a while and take time for me.  I am learning to take more time for myself but it is still hard since then I feel like my responsibilities are burdening other people.  On the 19th I had a dentist appointment and the dentist was happy to see that I am taking care of my teeth even with braces.  He was also able to let me know what the orthodontist was trying to do to help my whole situation.  It was a good day.  Rhett was able to get his braces off his top teeth that Thursday.  He has been waiting for this for so long, I mean he has had them on since 4th grade, it has got to feel weird having them off after such a long time.  It was nice to see that he could get at least the top brackets off, even though he had to wait until later for the bottom brackets.  The 22nd was the first day of U-fit for the kids.  They were excited to start that again, and this semester Dylan had a volunteer that he knew.  It was Itzel from JMS, she is one year older than Rhett, and she brought along two interpreters.  It was great fun for everyone involved.  I also finally got a call from the Jr high where Gavin goes and they wanted to set up a 504 meeting.  We set it up for a meeting for the 26th in the afternoon.  We finally got accommodations for Gavin!!!!  It only took until he was at a different school and older, which it totally shouldn't have taken that long to get seeing as he was tested when he was 8 years old and needed accommodations since then.  The next day was parent teacher conferences for Nikole and it was also the first time that she was passing all her classes at mid term. Dylan had a dentist appointment the following day and his teeth look great!  YAY!!!  Something positive for the month.  My dad had an MRI the last Friday of September, it was a follow up to surgery and a regular follow up with the neurologist.  The blood clot is clear and there is no sign of any other blood clot!  YAY!!!  Good news.  As I have been working I have had both my arms fall asleep while I walked around a room but it took hours for them to be able to have feeling again.  So I also went to the doctor's Friday.  They could find nothing wrong and sent me for nerve conduction testing and a MRI.  They never found anything.  The last day of the month Nikole took her bunny to the vet, they couldn't find anything wrong with him, but he is having digesting problems.

Sorry No pictures right now I will get some up as soon as I can.

Friday, September 4, 2015

Summer ends and School begins with LOTS of INFO

 So summer has gone and school has started I'm going to try to catch up on everything that has happened since I last posted about Rhett’s birthday. 
Family road trip.  Yes Rhett is asleep in the back of the car.  This is normal to the point that we had not even gone 5 blocks and he was out.  He will sleep for hours, and yes it is sad but this is life.
Rhett had an appointment with the cardiologists on June 15th for his cardiac cath because he has high blood pressure.  The doctor paged for me after Rhett was finished and told me that while he was under they gave him medication for his high blood pressure during the lab and the medication really didn't do anything.  Then he asked me if we have been part of Make a Wish before.  Geez!  This really sucks!


On the 18th we saw Rhett’s primary care physician(pediatrician) for his well-child, and Rhett told him that this last school year was a really hard because he is more tired than before, he can't seem to breathe very well, and that he sleeps more often and he's falling asleep in classes.  The list of what Rhett told the doctor just continues, but you understand that Rhett know himself rather well.  I sat there in dread because this is something that he had not told me anything about, even though I knew about it.  The pediatrician and the cardiologist collaborated and decided that it would be best if Rhett were mostly homebound this school year, because he cannot do a full day of school without injuring his heart by causing it more stress.  On top of making sure he is not turning grey and blue and purple because he is struggling at breathing while at school.  The pediatrician sent out a letter to all of Rhett’s doctors in June finding out what they thought about him being homebound and they all decided that it was important that he not completely be homebound.  Since being homebound is a very restrictive environment and they don’t want to restrict him from having a good quality of life, so they want him to be able to continue doing drama at JMS which he loves to do.  They also said that if he can take one class a day at the high school then by all means do it so.  We also saw the geneticist at the very end of the month of June.  It had been almost 5 years since we had last seen him so he was kind of wondering what was going on with our boys.  Like all the other visits that we had with them they took pictures and they told us that they presented the boys in several different places and nobody has seen anything like our boys before. Which we expected because they are just unique.  By the time we got to August the beginning of the school year was looming, and I still had not known what was decided with the doctors until about the 5th of August. I did find out that everybody pulmonology cardiology and pediatrician all decided that Rhett needs to be at home mostly, and they did put together a letter.  His pediatrician was representing all of them on what would be best medically wise for Rhett.  I had called an IEP which ended up on the 11th of August, which was the day after Rhett’s appointment for pulmonology where he was going to have a pulmonary (lung) function test.  The test on the 10th of August informed us that his lung function had decreased from 16% to 14%. That decrease was from March 25th to August 10th.
His PFT from March.
His PFT from August.
In case you need a little help with math that is a little over 4 months. I was expecting it to decrease because it always has and I'm sure always will. It was still emotionally really tough to get the information from the doctors even if I was expecting it. On the 11th at his IEP we gave them the information that we had, we also asked for him to be partially homebound partially in school and their response was it can be one or the other not both.  HOLY CRAP!!!  I DON’T NEED THIS!!!  It isn’t enough that his health is getting worse and he might die, let’s just do what we want not what the child wants. (Vent over for a little bit.) I am glad that I had gotten in contact with a AWESOME lawyer and was told that they can accommodate him and to set up a different date to have his IEP.  It was rescheduled and the plan was to get them to accommodate Rhett.  For those that are in education this isn’t trying to getting you upset or hurt you I am grateful for everything that you do.  Just a word to the wise, DO NOT CROSS A MOTHER AFTER SHE HAS BEEN TOLD HIS SON’S HEALTH IS BASICALLY FAILING. Get this a day after the supposed IEP Rhett had an appointment with the dietitian who blames his pulmonary function test decreasing on his 4 pound weight gain.  I was appalled that she would even consider that.  That 4 lb weight gain was from June until August and I was surprised that it wasn’t more seeing as we had family out and Rhett had a birthday and everything. So I had to explain to her that Dylan’s lung function also went down even though he did not have a 4 pound weight gain.  What a stressful week!!!  I was planning on having a fun evening trying to forget everything that happened that week with my friend Crystal (who I think is amazing!!!), But when I went to leave the house I looked at Rhett and noticed that he was breathing really hard and he was a little pale and blue.  I had to stay home and make sure he was ok, and force him to have a breathing treatment since he doesn’t like them.  On top of a breathing treatment I also had to give him a lot of extra encouragement to turn up his oxygen.  After all that and some time he did feel better but it was still frustrating because I still have had that opportunity to just relax and have fun with my friend.  The things that are given up for our kids.  On the 19th he started school at Skyline that one class every day.  I was picking him up and dropping him off that first day.  Then I found out that his aide will be coming to get him before class every day.  I did a happy dance when I heard that.  The next day was the first day of drama and he was able to go.  He love his drama.  We set up another follow up IEP after the one attempt on the 11th and we had that IEP on the 25th of August.  They had to have the assistant superintendent come and the compliance person.  We invited the lawyer that we had been working with to be there with us.  They finally said, alright we will support you at home.  But because we are doing that you need to do electronic high school with 30 minutes of home support a month.  Which for right now I'm okay with if they can give it to him in packets and as long as he has access to his email to email teachers with concerns and problems that he runs into in his education online.  So for now he is picked up every day from home around noon to go to his class at Skyline.  Then from there if it is a drama day he will be able to go to drama and if it isn’t he will get a ride home on the bus, or I will pick him up.  That is a lot of what we did over the summer for Rhett.  That is just a summary. I just couldn’t go into everything like I wanted because so much has happened.  I am still working on trying to find out where he can get his math, English, history, and science.  Who know how long it is going to be before he actually starts those classes.  Rhett was my helper when I tie dyed some shirts for all the cousins and myself.  Since I like color.  I would have gotten pictures before washing them all if I had thought about it sooner, but I did get them all after they washed.
He is always tired and sleeps often.
Told him to check his Os.  He wasn't very happy with me for asking him to do that, but he did.
When he is laying down this is what he was at.  Working a little hard to breathe, and as soon as he sat up his heart rate went up to about 120.  Not sure I like that number, but there is nothing that I can do about that.
Abby
Josh
Benny
Daniel
Mine
Gavin
Levi
Kofi
Dylan
Ama
Caleb
Nikole
Rhett
After being washed it was a great day to dry them.
My sister is awesome!  She took us out to dinner while she was in town.  I was not expecting it but my kids were sure happy to hang out with cousins and I was happy to hang out with all the rest of them.
Best picture!!  We were first at the restaurant waiting for the rest of the family.
Now the playing ensues.
Can't get enough as they were trying to out due each other.
All of them were so happy.
Crystal and I had a booth at the Angel's Hand Foundation motorcycle firefighter car show. This was for the non-profit that we set up this year.  We were able to talk to may different people and we were able to give all but 6 cake pops to those that we met.  We had a lot of fun.  My super helper went with me and helped set up and hung out until daddy came with the rest of the kids.
Here we are finally ready!
Our amazing booth!! With all the cake pops too bad we were ready before it started. LOL!
MINIONS!!!!  He was so excited!
Had to give them both hugs.
A quick pose before they were on to the next child.  But look at Dylan's face, so happy!
I am proud to present "Batman"!
Missy Nikole has had a full summer she went to girls camp and she also went to Brighton camp which is another girl's camp enjoyed both of them a lot.  I thought she was looking forward to starting school 8th grade being up at Churchill instead of at Northwest, which I don't blame her, less kids is always fun especially for junior high age.  She has since decided that she would rather not do the work and would like to change her classes.  Too bad for her is that I know she can do the work she just needs to do that.  She really enjoys school even though she is in all honors classes, she does struggle sometimes but not as bad as it could be right.  She has been struggling with being the only daughter, but she's starting to realize it's not that bad sometimes, only sometimes though. I have had good talks with her about her brothers and especially like with Rhett’s health and what's going on with it.  We are very open about things going on in our house, and things going on with us personally trying to make sure that communication is always open. That way they know they can always come to us with problems.
Dylan refuses to sleep in a room all by himself .  When Nikole is gone he would rather be with Gavin 
They are too cute together.
Gavin on the other hand is a whole other story and he was doing great for a while and then just exploded over the summer with anger and frustration. I'm not exactly sure what happened it got to the point where I did have to call the police on him, because he was out of control and raging toward me and toward his siblings.  That was everyone in the house at the time.  When that happened that was actually his birthday, which was really really sad and broke my heart.  I really didn’t want to have to do that, but he needs to understand that he cannot do stuff like.  I feel like this is going to be a slow process for him to realize and accept. When the police finally arrived they ask if we're going to be okay.  By then Gavin had gone to sleep which I am very grateful for, but before he did he broke his bed and he broke a few other things because he was just really really mad.  Since his bed was broken he ended up sleeping on the couch for about a week until we can get a new board in order to fix his bed.  We had him help with all that so he could see what it takes to fix something he breaks. So when he pitches a fit and gets explosive with anger and outrage it is easier to remind him of how much it cost to fix his bed.  I usually have to remind him that he will be fixing it himself again then he stops. I'm grateful for the opportunity of teaching him that he can't break things and just get away with it. Also by throwing a fit it is not helpful, respectful, or appropriate. He started off the school year kind of rough.  I honestly think they should have back to school night before school starts that way he would have an opportunity to meet his teacher and go over classroom rules and expectations before the first day.  For him it is much more helpful to have a heads up.  Sadly he didn’t have that this year, so the first day he ended up getting really frustrated.  He said I woke him up way too early and fell asleep for 5 minutes in class, and then his teacher nitpicked him out about that after school.  So he asked me to get him up a little bit later.  I have been getting him up a little later but in enough time to get to school on time.  He has done better, but still refuses to do homework.  Sigh, I think as long as he isn’t doing badly what is the point.  I have to pick my battles with this one. GRRRRR…..
Pitching a fit at the doctor's when I took him in for his well child.  Mostly because I had to let the doctor know what had happened on his birthday and it was bringing up not good memories.
He did ask me to delete this picture, but he is so cute I just couldn't bring myself to do that.
Dylan is just one of those kids he's always smiling always giggling and always laughing so happy unless he's being picked on, but for the most part this summer's been great for him.  He's had to play with his siblings, he has had time to just chill for a while, because with him and Rhett being the way they are they don't get to do too much.  What they do get to do is very important to them, that's a lot of us needing to stay inside.  We have been doing our best to just relax so that way we're not putting an extra strain on their bodies.  Mr. Dylan just loves playing with Gavin, he adores Gavin.  He also loves group hugs and he likes to be the monkey in the middle and have everybody grab around him and give him hugs.  He is such a lovable kid.  I am grateful that he was my last baby.  He is like putting a period at the end of a sentence.  LOL!!  On the the 21st of August I picked him up from school it was a Friday and he was so excited to see me.  He was giving everybody he saw a hug.  So for every person that came out of the building he was bound try to give them a hug.  The reason for this behavior was his friend’s birthday and he was just so excited.  He told the director of the school that he was giving everybody hugs because it was her birthday.  What a cutie!!!
He lost his first tooth!  He was so excited, but then that excitement turned to worry that he would lose all his teeth and not get any teeth back.
Trying to get a cute picture of him is too easy.

After getting all of the horrible news in June between the cardiologist and the pediatrician, I decided I need to try to figure out what I can do from home that way Rhett is not by himself during the day while he was at home.  I went to a meeting that a friend invited me to go to.  I found out that he and several people that I am now good friends with are real estate investors.  Well I am also a real estate investor but I never considered it too much.  After meeting with him and all these other people I figured I would have the support and encouragement I need to build my portfolio.  I am grateful to come along and get the support that I need to increase my investments to the point that my kids can work for me and get paid to do what they do for me.  On top of being home and having the freedom to take care of things that I need to take care of.  If you know anyone that wants to also real estate invest, or needing to sell their house please contact me.  I have only been part of this community a few short weeks so I am fairly new.  Even so I am loving it completely. 
CASHFLOW!!!  Love it!!  If you ever want to play let me know.  It will help you figure out how to think about money.
Every time I go over to Crystals house my cute little Daenerys friend just cannot get close enough.  She thinks I am stressed all the time and I am so happy to know that she cares.
One of the many times she cuddles with me.
Yes my sister is fun and amazing and love to go to the store with me in the middle of the night.  We have the whole store to ourselves, it is AWESOME!!!  Oh BTW Emily our produce friend wishes you would come back, he says we light up the place with our giggles and jokes.
One of our many middle of the night Walmart runs.
On a totally different tangent I had a fun summer with my sisters.  We are a crazy group, but it is nice having such great women to be related to.  We were all able to go to our family reunion in Idaho and these are some funny pictures that we got while we were there.  It was way too much fun!  Love you Emily and Hillary!!!

We were practicing our fish faces. LOL!
See we needed all the practicing we can get.
You know how hard it is to hold a fish face and not laugh when everyone else is laughing?
Oh idea time is coming up!
I am expecting TWINS!!!  How lucky am I?!?!
Honestly couldn't stop laughing!
The last picture before the TWINS arrived.  How exciting!!!
The TWINS have arrived!!!  Baby Mel didn't survive more than 2 days and baby Malaika is doing wonderful.
As the summer drew to an end we were bless to be able to take the kids to Cowabunga Bay with the Mascot Miracle Foundation and with Angel's Hand Foundation.  The kids enjoyed it both times, but with them there is no way we could have gone and done something fun like that.  They were only a weekend away from each other but the kids loved being able to go and be "normal" for a little time.  Nikole and Gavin found out that the water slides have cold water on them, but they still enjoyed going.  Here are the pictures I was able to get while we had fun in the water. 



I was surprised to see the "Zoo" playing in the water too.
I was awesome to see them coming down the slides. 
And he was all wet. LOL!!!
Need a hand?

Next?


Not even phased. :)

Watched to see what was going on.
They didn't even see me.
What a good sister the boys have.

That has got to be hard to walk in water in fur.
The kids thought it was so funny to see the "Zoo" walking around in the water.

Wondering the river.
Ha ha! There are all three of them!
You can see them all so much better here.



Who can hold their breath longer?

He wants to play too.

Who is the winner?












Love how they are social creatures.  They spotted the kids.

Dylan loves hugs and is grateful that he gets hugs.
Knuckles!  Caption this picture.  LOL!!
Pose for the camera.


The bear needed to have some attention too.





What awesome buddies!!!



Swim Dylan!!  What a helper Nikole is for her brother.


Ready?
I am totally missing a child.


Gavin is in the background.



Rhett wanted a picture of this.
He said to get a picture of the buckets dumping. Not a great shot.

Ok so this shot is looking pretty good.

Bring it on, FIGHT!

Oh kid caught in the middle.


Circling each other.


Trying to be the referee.


I dare you to bring it on. LOL!

I am ready!!!!  Bring it!!!
Charge!!!!!!!
You missed!

HA!



Wonder how heavy those costumes are after being in the water for that long?  Thank you MMF!!!
Back again and enjoying it.  Thank you AHF!!!

Yes he looks tired.
Ready to play!!!!
We came across this "bike" while we were running from one place to another on a Saturday this last month during our last summer good bye.
What kind of bike is that?
We also went to the zoo with Crystal and her kids for the last summer farewell before all the kids went back to school.  The only picture I have are these below. :)
Those boys are too cute together.
Crystal and I hanging out.  Man I miss doing that.  I think I need to hang out more.
This was our summer in a nut shell.  There have already more things going on that I need to update on but this post is already really long.  Sorry, but I have been going a million miles a hour.  I will be better, at least I hope I can meet my expectations of myself.
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