So as I suspected Jude was much older than the other babies at Gymboree. He also could not do as much as they could, BUT never the less he loved the class. He especially enjoyed the parachute!! I think he enjoyed the breeze in his face, and the texture against his skin. So we will be taking him back next week.

The people that own the place are so nice, and welcomed Jude back with open arms. I (of course) immediately shared with the class when we were introduced that Jude suffered a stroke. This #1 allows people to understand what is going on with him, and why he cannot hold his head up. #2 always provides an opening for someone to ask "babies can have strokes" (which I heard), and therefore I can educate on pediatric stroke awareness. Overall, I am happy we took Jude, and I pray that he will someday be able to use more of their equipment. Time will tell what Jude will accomplish.






Yes, Jude is in his Dallas Cowboys outfit, because again I reiterate that Football season is around the corner. Now if I can only convince Jerry Jones this broke girl needs some tickets to just ONE game...(giggle)

I would like to start today's blog out with a picture of my baby's natural mohawk. That's right, his hair is now so long that after his bath it stuck up like a rooster!

Although, I think a little mohawk would be cute on him, the boy needs a hair cut. I sent the picture to my husband who is adamant I am not cutting Jude's hair, and I did not receive a response.

So one of my best friends, and co-workers is pregnant. I have talked about her before, and how excited she is about her baby. Today she had her gender sonogram, and I found myself on pins and needles. Last night I literally sat in my bed praying that everything was ok. I didn't expect to get so nervous, about her sonogram, but I guess all the old feelings rushed back. I remember being like her, looking at names, and being so excited about my level 2 sonogram. Mike, and I went in with great expectations, only to be told something was wrong. No mother should go in to find out if she is having a girl or boy, and come out knowing something is wrong with the child they are carrying. So she texted me that she knew what they were having, but she won't tell me, and that she was waiting on the doctor to come in. Over an hour later I had not heard back from her, and I literally got very very nervous. I knew in my heart everything was fine, so I guess this was a reaction to my own prior emotions. Luckily, all was well, but the woman still won't tell me what she is having. I am just so thankful her baby looks happy and healthy!! Now I just need to know what she is having so I can buy her outfits.

So reflectively I looked back on a perfect sonogram picture I had prior to our gender sonogram, and before we knew anything was wrong. Little Jude on his tummy made me smile.

It's hard to describe to anyone the feelings of being told something is wrong with your baby. It's overwhelming. It's lasting. It's haunting.

Today Jude is trying out Gymboree again. I will take a lot of pictures, and we will see how he reacts with the other babies. I reminded Mike that he cannot look around envious of the other children that are "normal", but to look at Jude and what he is accomplishing.

Another busy day....

I feel out sorts because I am so busy this week. Work was been unrelenting, and I have had stuff to do on lunch, and after I am off for the day. I am currently taking a 10 minute break because I need to de-stress for a second.

Jude had a rather long seizure last night while we were visiting my dad and Kay. Kay said a nice prayer for Jude while he was going through the motions. Jude has a few spasms throughout the day, but he rarely has a long drawn out seizure like he used to. This one lasted about 15 minutes, and even though he did not yelp I could hear his breath become forceful with each crunch of his body. Jude's next neurologist appointment is in August so at that time we will discuss further medication options. I know it sounds like Jude's medication is always changing, but thus is the roller coaster we ride. I informed Kay, and Mike both about the bone marrow stem cell study I mentioned yesterday. Kay said she believes if any stem cell would show promise in neurological issues she would think it would be from Jude's own bone marrow. It's all scary, but fascinating. IF there was a possibility that the stem cells could help with his seizures, then that would be wonderful, but who knows.

So I mentioned I would share Jude's first bday party invites. I generally order invitations early because if people's schedules are as busy as mine, I figure they need plenty of advance notice. In addition I have several showers, a wedding, Jude's bday, and Ems bday coming up...whew. So here are his invites, hope you like them.
Front ~

Back ~


I would also like to share some pictures of Jude in therapy the last few days. It seems he is still making progress with his head control. His lovely therapist Leah brought Jude a brand new shiny bouncey ball to balance on. He loves his new ball!



Jude is going to try out Gymboree music and play again tomorrow. I will be sure to let everyone know how he responds. I am going to meet Mike, and Jude at lunch time so I can participate with them.

One last thing I would like to share. Emily completed an interview with "Kids who inspire", and I would like to share it with you. http://www.kidswhoinspire.com/emilys-smile-boxes-interview
I hope you enjoy it, I did!

Also, I received my blood results from the hematologist that completed all the testing months ago. If you remember I was informed I had some sort of platelet disorder, but there has been no further testing since. I knew I would need my tests for the pediatric hematologist we are seeing for Jude, since she does in utero stroke research. When I received the paperwork I scanned through the results. Under my bleeding time it's marked not as high, not as an issue, but critical?!? That word seems a bit concerning, you would think they could use something less....dramatic. Anyway, I am trying to find out who I see to narrow down what the issue may be. I love my hematologist though, so I am confident I will find the right person to isolate what the problem is.

Quick update

I have been unable to post an update today because I have been crazy busy at work. I will tell you that Jude is currently at 12 ounces today, which isn't much. Although each bottle has been full of rice so that is extra calories. Mike sent me some great pics of Jude at home with his therapist from ECI. She brought a great ball for Jude to work on today, and Mike said Jude enjoyed the therapy session.

I also received an email from senior research nurse with a university. She stated they will be conducting clinical trials in 2010 using bone marrow stem cells for treating brain injuries, CP, and hypoxic ischemic events. She wanted to keep Jude's information on file, and I find this very encouraging. I am apprehensive about extracting Jude's bone marrow, so that would be something I have to really think about. It was nice to have someone contact us, about future possibilities though. I will be interesting in hearing all the pros and possible cons to the procedures.

I also received all of Jude's medical records from his neurologist. It's the first time I have read in bold dark writing "Intrauterine stroke noted". I guess I always think maybe there was something I just did wrong, but there it was in black and white. it was also referred to as a prenatal cerebrovascular incident. What was strange was I received the above mentioned email from the nurse, and I remembered I read hypoxic ischemic event in Jude's medical report somewhere. I believe that is a overall lack of oxygen to the brain, which Jude's stroke caused. It's a little confusing, and I will have to read back over his records, but I am sure it said that somewhere. Anyway, the medical records are just opinions, but they are interesting. Plus, I find this doctor's information a lot more positive than the last dr we had.

I am off, I will hopefully have a chance to update more tomorrow with pictures.

Are we doing enough?

I am happy to report that Jude has taken 16 ounces so far today, and a 1/4 jar of baby food. He also had some play time with his "reward" fan. Jude's therapist brought him a large red button, and if Jude hits it it will make his toy fan light up, and turn. Jude seems to understand that hitting buttons provides a reward. I found a website the other day that provides several of the "walking" stuffed animals that attach to this very same button. I am hoping Jude will receive a few animals from family members for his bday. I received his birthday invitation I created, and I will have to scan them for everyone to see.

Sometimes when I read the blogs of other special needs mom I feel like I am lacking the therapy dept for Jude. I see such neat adaptions, and equipment they have for their children. I am not sure if it's a failure to research on my part, or a failure on one of our therapists part. Although our wonderful therapist Leah is meeting with the medical equipment specialist at the end of July to fit Jude for his adaptive stroller. At that time he will also have a bath chair ordered, and I hope he can obtain a tomato chair. I sometimes read these other sites wondering how long it took for their children to obtain neck control, Jude shows so much promise, except for his neck. I know Jocalyn will smack my hand for reading other blogs, and being emotional.......smile. We work with Jude constantly on keeping his head up, tummy time, reaching, and more. I feel a bit held back because he doesn't have the necessary equipment yet, but he is still little. One thing I am pushing with Mike is to take Jude back to Gymboree. We got side tracked from his music/movement class because of his hospital stay, and just never took him back. I am hoping the owners will understand, and not have us pay another enrollment fee. Just loved his Gymboree class, and now that he is more aware I think he would truly enjoy it.

So I know my brain is going a million directions lately, but I guess that's going to happen. So let's lighten the mood, and I will tell you about Jude's crazy hair. Mike and I agreed not to cut his hair until Jude was 1 year, but come on folks it's getting out of control. So I gathered his hair into a nice purple pony tail holder on the top of his head, and took him to Mike to make a point. The pony was swiftly removed, and I was quickly reprimanded. Next time, I think I will try pig tails.

Mike is currently working with Jude on keeping his head up, and opening his hands. I am going to go help him.

Just let me be

As I stated earlier Jude is doing better, but he is not a 100% yet. He has eaten enough today to stay hydrated, but nothing more than that. Which means he is doing what he needs to, to survive but ....nothing more. He fought me tonight when I gave him his bottle prior to putting him to bed, and I truly hurt his feelings when administering the Depakene. My friend "Fleck", was here, and got to experience the hissy fit in it's entirety, crocodile tears, big lip, and all. Surprisingly even though there was a fight I quickly got Jude's medication down him I included a few sips of apple juice, and a few sips of formula, before I let him retire for the night.

The ever looming issue of keeping Jude nourished is becoming a huge monster waiting for us. It's like we climb the mountain ahead of us only to find a huge obstacle standing in our way, it's a slap in the face. Jude has had a swallow test, and we know that he is not aspirating, so this is just a flat out refusal to eat. I have issues with a G tube, but if need be we would obtain one, but I hope we don't have to travel down that road. I admire you mothers that have ventured in that direction, but at the same time I selfishly hope I don't have to check into that lesson. I hope that doesn't offend you.

As mentioned my friend Fleck was over tonight watching TV, drinking wine, and talking with me. It's amazing how fate steers the appropriate people your direction in time of need. She sat with me on a Saturday night watching my baby cry, and she ate my chicken casserole.... that I probably baked to long. I explained to her tonight that I tend to be rather trusting, and naive when it comes to friendship. Yet in her case I know she is genuine, and she listens to my issues with an open heart. I told her all about my friend Ginger, my oldest... and dearest friend, who has always done the same. I explained that if I was wandering alone in the middle of the night crying Ginger would take me in and wipe my tears, without question. I know Fleck would do the same with hugs and little questions. My cousin would also do the take me in, and if the situation needed, find the person who created the tears and SMACK them with a sock of quarters. It's nice to have people who can listen without "advice", and just let you be. Just let me be..........me. Regardless of a mention of names my friends are always there for me, and I am grateful. When I leave this Earth I hope to leave behind smiles in people's faces. In other words, I hope my friends will think of something I have done, or said with them...............and smile knowing, "Well that's just Jenn". That would make me happy!

Sometimes I do need to just "be" without agenda, or reason. My life may seem together, but at times it is very frayed. The first year is the hardest.........so I hear............I hope they are right.

Better

Jude slept well last night, and even though he didn't take a lot of formula, he still ate. This morning he woke up a little before nine, and ate 6 ounces with rice...what a relief. He stayed awake for a few hours laughing, giggling, and playing on his blanket. He is now sound asleep in his bed, and I am about to clean Emily's closet. I am relieved that Jude is acting more like himself, and even though I know eating issues will approach us again, I feel much better. Sometimes I think Mike would literally break if he had another week stay in a hospital, but I also understand he would make it through. I also hate seeing Jude getting Iv's, and being poked, and prodded. Maybe Jude could sense our worry, and forced himself back to normal. Regardless, I am thankful that Jude is smiling, giggling, and eating.

The stem cell subject has now shown up in several support groups I am a part of. It seems there are several other mothers that either banked their cord blood, or did not. There is even one mother who has had another child already, and banked their blood with the hopes Duke U, or someone else will be performing sibling to sibling infusions. According to Duke U they will be approaching this subject or donation cords in the future. My understanding is whoever performs the infusion must extract the stem cell out of the cord blood to make sure there is no reaction. Although, I am not a medical professional, and only relaying what I have read. Regardless, it's all very fascinating. Ellen announced that Max will be receiving his infusion in August, and I will be following his blog closely.....I always do anyway though.

I am off to make a pot roast, and invite my family over tonight. I made some invitations for my sister wedding, and everyone needs to look at them prior to ordering.

Yet another update

According to the pediatrician Jude is not hospital bound because he has had 1 wet diaper in 12 hours. The doctor looked at Jude's ears, listened to his lungs, etc, and finally determined this is either teeth, or viral. He left a couple off though because it could also be neurological, or medication related. It's amazing the difference between doctors, because I know the neurologist would have admitted Jude asap. I cannot say I am upset that he is not in the hospital because it's very tiring there.

I understand the pediatrician is unsure how the seizure medication works, but I do trust his judgement. We will be keeping a close watch on Jude, and if anything changes I will not hesitate to take him in. The great news is that Mike brought Jude by my office after the doctor. Jude was sleeping, but I was able to wake him up, and get him to take 4 ounces. That means since 8am he has had 9.5 ounces, but it's something!!!

Thanks for your continued thoughts. I will update this weekend. Now I just remembered that the adaptive stroller guy still hasn't called me back, so I am off to call him again

Fever update

Jude was a bit cranky last night, and poor Mike got little sleep. Honestly, neither one of us really slept that well, but Mike was insistent in staying up to get Jude to eat something. Since I have to get up and go to work, Mike takes Jude so I can try and sleep. I had worked with Jude until about 11pm, but he would take little more than some drops of Milk in his mouth. I tried some teething gel, but he did NOT like that at all.......I mean at all! He let me know for about five minutes he didn't like it. Jude's fever got to about 101.7 before time expired, and we were able to give him some more Tylenol (he had some earlier in the day), which brought his fever back down. I also put him in a luke warm bath, and let him lay there for a few minutes, which he was rather unhappy about too. Normally fevers do not bother me that bad because I know they are generally just doing their job, and fighting an infection. In Jude's case it may just be teeth, but again with Jude it's always a question of normal baby behavior, or life threatening. With Jude a fever can be very dangerous especially if he is not eating. Jude had about 2 ounces at midnight, and then had 4 ounces at 8am. So he is still eating, but not much. In addition to that he has loose stools, which contributes to dehydration. If Jude dehydrates his seizure medication can become very dangerous for his kidneys, and liver. So Jude's situation is different.

Emily used to run very high fevers when she was a toddler. In the morning she was fine, and by lunch time she would have 103 fever with an eardrum about to rupture. I would never have any warning she had an ear infection it just seemed to be instant. Em's pediatrician was never really worried about fevers, even when hers got to 105 one day. The high fevers made me uncomfortable, but again I learned they were there for a reason. With Jude it's like relearning life, and that sometimes throws you for a loop. Ear infections were Em's only issue, and they caused 7 ruptures ear drums, and 30 percent hearing loss in her right ear, prior to tubes in her ears. It was a nightmare, but nothing compared to Jude.

So I would prefer to be at home with Jude, but I need to work today. I set a doctor appointment for them at 2:15, and I will be waiting to hear. I also sent an email to his neurologist letting him know we were going to the pediatrician. I was unsure if he wanted Jude's pedi to check his blood for his Depakene levels, or not. I figured it's better to cover all the bases. I am still hoping it's just his teeth.


*** Update ~ Since 8am, Jude has only taken an ounce and a half. I am beginning to feel we will be spending another weekend at the hospital. I am frustrated that I am away from Jude, I feel like he needs me.

fever

Jude has a fever of 101.5, but I am not sure if it's teeth or another issue. Jude rarely runs fevers, and of course he isn't wanting to eat or drink. I am mildly concerned this may be an issue with his Depakene so we are keeping a close watch on him. I will keep everyone updated.

Stress Stress

Poor Mike was so upset by the time I got home yesterday I thought he was going to burst. Jude was not eating like he should, and crying constantly, therefore increasing Mike's stress level. By the time I got home they were all so worked up I could cut the tension with a knife. So I tried to keep as calm as possible determined I was going to get Jude to eat. Mike was upset thinking that Jude was going to have to take another trip to the hospital because we had less than an hour to get liquids into him. Without liquids Jude's seizure medication can cause serious issues. So I gave Jude some Tylenol thinking this may be another teeth issue, and I laid him down for twenty minutes, while I took a bath to wash off any stress. Once I got out of the bath I changed Jude's clothes into a comfortable onsie thus waking him up. I then warmed his milk up so it would be easier for him to take, and sat down taking my time getting him to eat. He ended up eating 9 ounces in one sitting. I am sure Mike thought I just think I know it all, but I didn't. It was just a change of people, and a change of scenery. I am sure Mike's stress level contributed to Jude's stress level, and they just needed a different person to step in. In this case it was mommy, and Jude snuggled with me for a long time, he didn't want to be put down. This insured me that it was his teeth, and he was just hurting.

After Jude ate, and had snuggle time he was ready to play. I put him in his crib while Mike and I watched a movie, and I kept hearing his famed barnyard toy go off. After I would hear, moo moo, peep peep, I would hear a shrill laugh, and then the toy would start over again. That crib toy was the smartest thing I ever bought. I would like to confess that the rest of the night went wonderfully well, but little Jude decided to play night owl again. About 11:30 I called for Mike, and he came to entertain Jude for a bit while I slept. They finally came in about 1:30, and Jude was still asleep when I left for work this morning. I know it's so stressful for Mike at times because Jude's situation is not normal. Would I prefer to be at home? of course. Am I thankful for my job? 100%, but I still miss my children. I also know Mike needs a break sometimes.

So while upset last night Mike said he thinks the stem cell possibility is chasing a unicorn. I don't really think he feels that way, and with investigation I think he will find what promise it has. I believe he feels he is betraying Jude if he researches the information like he wouldn't be accepting Jude how he is. It's a matter of accepting Jude, but seeing what may benefit him to help him have a better life. We do that with all our children........don't we? I did talk to a company yesterday that is extracting stem cells from full term cord blood. Since the cells are actually extracted from the blood and then infused there is no reaction. This plan is ran by three doctors, and they are going to evaluate Jude's medical records, and give me their honest opinion. They are looking at everything for free, which I thought was very thoughtful. I did some research on one of the doctors, and found a multitude of write ups on him, and videos. The cases and success stories are amazing, one of the cases was a blind CP patient who could not speak, can now speak, and see. I understand though that for every success story there is probably a failure. Regardless, it's fascinating. If Jude is ever a candidate I am not sure how we would afford the infusion. I guess we could hold a large fundraiser like some other families do. Can you imagine how great Jude's case would be for research?? I mean I have tracked everything from the very beginning, and to then follow a possible stem cell infusion, and whether it shows some form of success, or not it would be interesting. In my eyes Jude has already helped other moms, children, and families, and maybe this information would be helpful too? To help data on whether stem cells can help with those neurologically affected, or whether they cannot.

So Em is still practicing her softball, and we let her batting coach know she didn't make the other team. He seemed very frustrated that the coaches did not complete a practice swing prior to starting the batting. He then explained to Emily that any time she tries out it is reasonable to ask for a practice swing, and then advise the coach if the machine is pitching the balls to high or low. He explained that "there is no coach that would want you to swing at a poorly thrown ball, so why would you in try outs?". I explained that the primary reason she didn't make it according to the coach was her fielding, and grounding. He then told her she has to reach, dive, and get under the balls. I explained we were thinking about bumping her up and putting her in 12u rec, but he didn't seem that happy about that. I think he wants her on a team to improve, but that's easier said than done.

Here is a picture of Jude from last night, I love his cheeks!

A night awake

Yesterday after I wrote my blog I continued to work my booty off at my office, and when given time I researched a bit on stem cells. I put a call into Jude's amazing neurologist, and he returned my call around 5:30 when we were shutting down. He sat and talked with me for awhile regarding his thoughts on the stem cells. He seemed interested in the conversation, and replied the best he could. He said that he is not well versed with stem cells, but he does believe that if children like Jude will have a shot at reconstructing their brains, it will be through stem cell therapy. He explained that he felt like the medical community was truly held back by Bush's lack of support in the stem cell area. I told him that I asked a doctor about banking Jude's cord blood, and I was told that it would help with illness, but there was nothing that could reconstruct the brain. I think he thought that was rather comical since stem cells work as building blocks. Although, he did point out that there is no guarantee that the positive changes they are seeing are due to the stem cells, and they must get more science behind the research first. I then asked him why they cannot use donated, or sibling cord blood, and he explained that the immune system must be compromised for donated blood. So they will not use anyone elses cord blood unless it's a life threatening situation, which makes sense.

After that call I felt a little down because I understood why they cannot use donated blood. In addition Mike and Emily had been hit from behind, but were luckily ok. So it was a crazy day, and I was anxious to get home. Once I was resting on the couch with Jude I kept looking at his little smile, and I would smile back. I thought about how I love him just the way he is so if I cannot get stem cells for him then... I just cannot, and it will alright. Although, if there is a chance that I might have the remote possibility of improving his quality of life, I would. So I played with Jude for awhile, cooked Em some dinner, and just hung out with my family. It was needed after my whirlwind of a day. I am afraid I woke up about 2:50am due to Emily's meowing cat, and could not go back to sleep. I am not sure if it was the stress of the day, or having to much on my mind for other reasons.

Once I got into work today it was strange, there sitting in my inbox was a request on twitter from a stem cell institute. Not only was it an institute they focus on placenta stem cells harvested from full term baby placenta that is donated. I almost didn't click on the link thinking that I would find the same old information, and feel worthless again. Something drove me to click on it though and I read through the plethora of information. I have always known that the placenta is full of amazing items thus why other countries have different traditions with it. Although you know what stuck out the most, "The placenta stem cells do not posses antigenic properties making the rejection of the stem cells IMPOSSIBLE". Oh my word! I read the diseases and afflictions the cells have been known to help, and cerebral palsy, and stroke were both in there. Who knows if this would help Jude, but I filled out the evaluation form. I have no idea how we would come up with the funds if they chose us, but I trust God will provide. I am sure it's very expensive. Oh, and the funniest comment today was from myself asking my co-worker/best friend Sarah if I could have her placenta after she gave birth in December.

On a happy note, and rather ironic activity Emily opened a fortune cookie last night and it said "A smile will be your passport to the heart of others". How true: www.emilyssmileboxes.com.

Here is a picture Em took of Mike, and Jude on the couch.

Stem cells, and major regrets.

I am so discouraged!

Back in April of 2008 when I heard the dreaded words "mild Ventriculomegaly" I went on the hunt for a support group. I found the following website, http://www.i-am-pregnant.com/encyclopedia/Babies/Ventriculomegaly&page=1, and met many amazing women. One of those women was my friend Amy (aka. Turtlemom) that frequents Jude's blog. She had a beautiful daughter Parker, and she about the same age as Jude is. Once Amy's daughter was diagnosed in utero with hydrocephalus she researched banking her daughters cord blood. Jude did not present with hydrocephalus, but rather what looked like a lack of brain (cortical thinning). I never ran across information on stem cells helping Jude in anyway. Amy, and I have kept up with each other because our children's situations are similar. Although, I must admit she has kept up with Jude's blog more than I have with Parker, and I am ashamed of that. I am now 100% to date with Parker's story. You see Parker also has bilateral schizencephaly, she has 2 cysts in her brain, and she had severe visual loss. Now? After the stem cell infusion.......... she is crawling, sitting, babbling, and she has her vision. That folks is amazing, and I am thrilled for her family. So sweet Amy emailed me asking if I had considered the stem cell option for Jude. I did consider this, and I asked prior to Jude being born if I should bank his cord blood. The doctor said we could in case of illness, but that it would be of little help to his brain damage (little did he know). I still wanted to bank his blood, but honestly with everything going on I did not. It was very expensive, and I think I was just overwhelmed. Parker's infusion was done fairly quickly after birth, so I am unsure if this has a lasting impact vs stem cell infusion later in life. That is a question I need to pursue.

So I called Duke university this morning, and talked with them about the program they are running. It seems Jude most likely would have qualified IF his cord blood had been banked. They would have used his cord blood to do a stem cell infusion. I then asked them if we can get donated stem cells, and they said no. My next question, was sibling stem cells, but she explained that at this time they cannot use sibling donations. I then asked her if she knew of another research program in the US, or beyond that would accept donated cord blood, but she didn't. My heart sank.

So what benefit are stem cells? Well Amy sent me this article about stroke recovery, and it's rather fascinating http://neurosurgery.stanford.edu/about/stemcellsfillgap.html. I plan on contacting the doctor to see if he has any suggestions. My understanding is that the stem cells can actually improve recovery. They are special cells that can become other types of cells, and work as building blocks within the body. There is no guarantee, but if your child had brain damage and even had a remote possibility of being able to walk, talk, or sit because of a low risk procedure, I am sure you would do it.

So would I have another child if they could use that child's cord blood? YES, it's a no brainer. Have I been scolded that I don't have the finances for this, yes. Although when it comes down to your child, and possibility improving or saving their life ........ well what's the question....you would do it. We would hope that we would have a healthy normal child, and be able to help Jude at the same time. Could I give Mike a normal baby? I would hope so, but the pregnancy would be FULL of stress and questions, although the child would be very loved. In the end there is no question, if there was a possibility this would help Jude, we would MAKE IT WORK. Second jobs, whatever it took......we would make it work. The possibility of this happening is very remote people, so I don't need opinions on it. My maternal side of my family has wanted me to have another child for a long time, but honestly I didn't want to. Would I have an issue with having another child? yes, and no. I have gotten myself in the mind set that this will not happen for various reasons, and I am very comfortable with that. So either way we would do what we needed to. I would stress about finances, because we owe so much in medical bills right now. Although, we are in a different situation now because Jude is receiving help through MDCP. Anyway, like I said......remote possibility, and as of right now no possibility if there are no programs out there. So let me stress as of right now this will never happen, it's just me working thoughts out in my head. I guess it's me dreaming of helping Jude.

I am very uneducated when it comes to stem cells, and maybe someone reading this would have more insight. I do know that in certain situations stem cells cannot be used. Anyone having a chromosomal deficiency cannot use their banked cord blood because the blood carries the same error the DNA has. Also in some situations when a child is sick, it will infuse more of the problem back into the child. Although Jude's issues are not chromosomal or illness, it's all due to the stroke. It's all very fascinating though, and amazing that the medical field can provide this treatment to others. Yesterday I learned that Max http://lovethatmax.blogspot.com/ will also be receiving stem cell therapy, and I am crossing my fingers for Ellen. Regardless, of what may happen to Jude in the future I think the possibility of these children having a chance at even partial recovery is WONDERFUL. There are no guarantees, but I will continue to hope for the best for them.

In the end I will pray, and hope that somewhere down the line Jude can benefit from this amazing procedure. I will continue to research, and follow programs that offer this. I will also not accept the immediate advice of some doctors that may not know the full benefits of stem cells. Jude may never profit from this new research, but we can still keep up with it, and see what advances are made. I can also kick my own butt for not following my own mothers intuition, and finding a way to bank the cord blood. That very well may be something I regret for the rest of my life.

To see the progress little Parker has made please visit her video here: http://www.youtube.com/watch?v=2P8LTCQkaGI. Her mom said she still has her coned shaped head, but she looks just beautiful to me!

Now there is my long rant for the day, and the emotions circling inside of me are many and overwhelming today. I have regret, a little hope, and just pure fasicination. Since Jude was diagnosed my life is no longer simple decisions. My life seems to be full of situations that wreak havoc on my brain at times. I am not just talking about the cord blood, because the possibility it may have worked could be zero. I guess it's just life in general. Sometimes it just isn't easy, but sometimes it's great. It's just the never ending tug of war between the two sides.

Monday

I am at lunch in my office so I thought I would post a quick update. I had a nice weekend with my family, and I think I really needed it. I got some quiet time with Mike which was nice, and always enhances our relationship. Jude was very talkative the entire weekend, and that made me very happy. Here is a video of him last night talking to his barn toy, and just having a great time in his crib. I really miss him today...


Jude's high pitched pterodactyl squeal cracks me up every time he belts it out. Sometimes I watch him laughing along with him, but I wonder inside about when he is older. I wonder if people around us will still look at him with love, or will his disabilities cause people to shy away. I am not sure Jude's drooling will go away when his teething stops, and it's always that unknown factor of what lies ahead. I guess I will have faith that people in general have a good nature about them.

Emily's dad had her this weekend, so it was great to see her last night when we picked her up. While she was out I put her boxes together for her next smile box drop off. That way she can fill them all this week, and get them ready. She was grateful for the extra help, and she even came home to a donation from our friend Fleck. She brought over to huge tubs full of beanie babies to put in the boxes. I am sure Em is at home getting all the boxes together because she plans on dropping them off to Children's in Dallas on 7/25.


So I am still in pursuit of Jude's adaptive equipment. It's my understanding that the person who will be fitting Jude did get in touch with Jude's therapist, but I have not heard from him. I just placed another call to follow up, so hopefully I will hear back from him quickly. That means Jude will be fitted for his adaptive stroller......which is basically a wheel chair, for right now. It will keep his head supported, but I hope someday he won't need this. He will also get a bath chair, and I am hoping a tomato seat, or chair of some sort. I am hoping that at some point I can get the carpet out of our living room, which will be easier for the stroller. Anyway, Jude ate very well this weekend which is so great. He is still working on eating solids, but he is now taking plenty of formula loaded with rice. He is growing, and I can tell he is looking more plump. Take a look:


I am a bundle of nerves today about finances, and medical bills. I hate this part, but I am thankful for my family, my job, and our friends. I am also very grateful for a wonderful weekend, and the chance to re-coop a little. Now I am off to read some other blogs while I am still on lunch.

A Saturday full of giggles

Today we had a baby shower for one of Mike's best friends, Katie. Katie lives in Colorado, and flew in to have her shower, and see family. She looked beautiful in her colorful yellow strapless dress, and seemed to glow like expectant mothers do. I admired how thin she was, and commented how I never had problems gaining weight when pregnant. The most ironic part of the day is that Katie's mother is a NICU nurse. Her mother came over to us, and talked in length about Jude's prognosis, and current situation. She said she worried about Katie's pregnancy, but know the statistics, and understands she and the baby will probably be fine. I assured her I knew they would. Mike, and I have a long running bad humor joke that all our friends and family are covered because Jude took on the responsibility of being the statistic amongst them. I wouldn't have it any other way though, and neither would Jude. I am sure the joke is in bad taste, but there has to be humor in life regarding difficult situations.

Our little baby was as precious as ever today, and was very calm at the shower. We are so lucky that he is such an easy baby to care for. In our situation we are blessed that he does not need more medical intervention, and we understand this. He just seemed to wake up in a great mood today, and smiled, and talked to me most of the morning. Mike said it seems like Jude is a different baby when I am at home on the weekend, and like he knows I am here. That made me smile because sometimes I feel like a lacking mother since I work full time. It's the never ending struggle of wanting to be with your child, needing to work, and a lack of winning the lottery (smiles).

I just sat Jude down for a bit so I could type out this update. He has had a few spasms today, but overall seems to be doing alright. I know his teeth are hurting and I am sure that's causing the additional spasms. Jude was playing with me again while I held him on the couch prior to putting him down. He would lift his hand over and over to my mouth so I would kiss it. Our high pitched kissing noises bring huge smiles, and laughs from Jude, and these moments make our day.

I just made some homemade banana nut bread, and I made some brownies. We are going to my cousins to watch our men yell at the TV while watching the UFC 100 fight. Please have a safe weekend, and hug your children.

A let down

The good news is that Jude again slept through the night, the bad news is Emily did not make the select team she tried out for. Ahh the drama of kid sports. It turns out there were 13 girls, and only four - five spots. I thought there were around 8-9 spots open, but I was wrong. The coach explained that Em is a good little player, but still needs some work on some things. I know this, and she does need additional practice, but she is moving from rec to select so there are going to be issues. Each coach explains that Em doesn't need to go back to rec, but what is she to do if we cannot find a local select?? Anyway, poor Em is crying at home, but this is a part of life so it's a good lesson to learn. Also, she needs to learn that if you want something this bad you will do what it takes to obtain it. That means she practices without being told, and finds the time to improve her skills.

I am afraid if we put her back into rec, then Emily just will not improve as a player, and she won't ever make it to select. It's important to me because it's important to her. Select is a whole new world, and if you don't have a team that is picking you up to start with then it's a menagerie of excellent players. It isn't children that miss the ball sometimes, or miss a swing it's EVERY ball is caught, EVERY ball is hit, and EVERYONE runs like the wind. I guess it's like life, the only way your improve is to meet people that are better players. So now we must decide if she will continue to try out. I am considering continuing her lessons, and letting her play another season of rec, but bump her up to 12 and under. In fact, I am really leaning this direction. If she spends six months improving her skills then she will be a stand out at try outs. In fact, I am really leaning this direction. I am still holding out hope that her last coach, coach Brian will eventually form his own select team. He expressed interest in this, and in bringing Em on. This would be wonderful! I am sad for Em today, but I also think she learned a valuable lesson. In life we have situation that arise that require our full dedication, and sometimes you just get let down.

Jude was pretty fussy when I got home last night so we gave him a dropper of Tylenol. He immediatley calmed down so I know it was his teeth. I am going to keep this short today, but I did want to update.

Here are some pictures for you:




Jude finding his hand.......this is a good thing!

So much accomplished

I am making progress today in the search for Jude's medical equipment. Thanks to Jocalyn I found a very nice man at Allumed. He is contacting Jude's therapist to schedule an appointment for a "fitting". We have a prescription for an adaptive stroller, a bath chair, and a specialized car seat. I am not sure we need the car seat, but Jude really has very limited neck control.

We also scheduled a hematologist appointment for Jude on 7/30. We are meeting with a in utero and childhood stroke specialist with Cooks. I never knew they had a hematologist that specialized in childhood strokes, but that is encouraging to hear! I think this is a great thing. I went through a time where I think it mattered what caused Jude's stroke, or brain bleed, but now I understand it's necessary. I also followed up with my hematologist to finally find out what this underlying platelet disorder is they discovered after the pregnancy. I guess we will finally know if Jude has the same issue, if he has factor V leiden, or anything else. Our main concern is to make sure Jude doesn't have the potential of suffering another bleed. Seeing how when my platelet problem was discovered the doctor called me a "bleeder", I think it's a high possibility Jude could have the same issue. In addition to the hematologist appointment we also set up a follow up opthamologist appointment for Jude. We know he has gray optic nerves from lack of oxygen which has caused visual impairment, but we don't know the extent of the impairment yet. We have noticed Jude is looking at us more, objects more, and is very interested in bright lights.

In addition to all the above I talked with the Division for the Blind yesterday, and they will be following up on Jude's case. They can provide additional help as needed. Also, the nutritionist said she really feels Jude will only need her attention on an "as need basis", so we will not be setting up a follow up with her right now. So to say the least we have gotten a lot accomplished this week. I would also like to report that Jude is back on schedule regarding eating, and sleeping. When I got home yesterday he had taken over 20 ounces, and eaten vegetables with rice. He did wake up with a seizure this morning reminding us that we are still on the roller coaster. His seizure was quiet, but it was a cluster and lasted about ten minutes. The strange thing is he can smile through these clusters, which is a new development.

I would like to take a minute to share one of the reasons why I have written this blog every single day since April of 2008. Why I share personal highs and lows, and information on Jude. Below is a quote from Hope's mom at www.honkeyplonk.blogspot.com.

" this blog is for other mummies who may find themselves walking an unfamiliar, unchosen path. I was and still am privelidged enough to have followed a blog about a baby called jude. Jude is a few months older than Honk, but with similar diagnosis and prognosis. His mom blogged dàily; the highs and lows. Like Jude, hope was blessed with a good start, and at about 3 months began having seizures. If it wasn't for his blog, I may not have even recognised honk's seizures. I feel that although the path Im on is new, I'm slightly better prepared for the journey thanks to jude's mum. Perhaps then I can be the one to show someone else the way! By the way, though I said this wasn't a path I chose, if someone said they'd show me how to go back to the start and chose another path, I wouldn't! "

I am honored, and glad I could help in some way.

Time to go back to work, have a great day!

a nutritionist, and a softball game

While I was at work the famed nutritionist finally visited our household. Honestly, she came out as soon as she could, and according to Mike she was fabulous. She said that, "Jude is so much better off than many babies I see, even many adults I see". REALLY? Did these words actually escape a professionals mouth? No "prepare for the worst", no "wait and see", no "I just don't want you to get your hopes up", no "I am sorry it is not good news" ?!?!. Mike said she watched Jude hitting the red button turning his fan on over, and over, and that she seemed impressed.

She measured Jude, weighed Jude, and looked him over in general. She explained that you can tell just by looking that our baby is underweight, but just "slightly". We were told that we are doing the right thing by putting rice in every bottle, and that we are now suppose to add a slice of butter to each jar of baby food. This will add extra calories to Jude's food, and she had a few other tips for us too. On top of her advice she left us 4 cases of Good Start Carnation, which is different from what we currently use, but she likes the product. Also, this helps us so much financially, so we are very grateful to her. The nutritionist then when on to tell us that she suggests adding Pediasure to Jude's diet, but not until 1 year.

One year..............wow, Jude is about to be one year. This is both shocking to me, and then on the other hand the last year seems an entire lifetime. Today I created his birthday invitations, and informed friends that the official celebration of Jude's first year of life will be September 5th. After planning this I then took Em to try out for the select softball team she wants to join........only to find out the first tournament they are planning is the beginning of September......ugh. We will manage though.

Yes, Em tried out for a select team, and I liked the coach, and the players. There were 15 girls trying out for positions on this team, but there are only 8 spots. I could tell that Emily played her little heart out, but I could also tell that she was a bit nervous. The coach said that he is looking for "coach able" girls with great attitudes, and the fundamentals down. Emily really wants this, so we can only hope he saw Emily's amazing attitude shining through. I really liked the moms I met, although it's always awkward for me when I meet new people. I am sure I come off like a huge goof, but I guess I am, and so hopefully they are accepting of my true character. I took the opportunity to pass some of Emily's Smile box cards out. I figured if she didn't make the team, they might still remember that her cause needs some support.

Jude is still awake, and I am exhausted. I am about to rock him to sleep, and I will join him in slumber land. Good night all.

Fourth and Long

Last night when I got home Mike was again frustrated with Jude's lack of eating, and having to get Emily to softball practice made it worse. I think when he gets rushed it makes the non eating issue a huge deal, and makes it seem unmanageable. Honestly, Jude had eaten, but he seems to eat more at night than during the day. Once Emily and Mike got back from practice we sat down to eat a bit, and Jude played on his blanket. He likes to coo, and laugh while laying there, and I always wonder what he is laughing about. . Sometimes I feel sorry for Jude because of his issues, but he constantly reminds me with his sparkling laugh that he is happy, and that is all that matters. Depending on the severity of Jude's impairments as he grows he may never know cruelty, pain, or the other negative things in the world. I guess in the end.......that isn't such a bad thing.

So have I told you I love the Dallas Cowboys?? I do! My grandfather played in the NFL for the Bears, and the Giants years ago when they had leather helmets. I am therefore by nature a football lover, and my grandfather taught me to throw my arms up for a touchdown, by age two. It's a fond memory I have of my childhood. My grandfather always said he was conflicted when the teams he played for played Dallas, but in the end he was a true Dallas fan. He was drafted with Tom Landry, but they went to different teams, but he often talked of him fondly. Anyway, I love football season, and I am looking forward to the games just lurking around the corner. We have people over every night the Cowboys have a game. We make dinner, and everyone participates by bringing a dish. We then all crawl into Mike's bright Cowboy blue "man cave", and we all surround the TV. We yell, we scream, and yours truly has even fallen on the floor. Yep when Tony Romo fumbled the famed playoff ball I fell flat......I felt for him, but was so upset. My favorite football players are from my era, and I recall their games fondly because they were.....the "dream team". They consist of Michael Irvin, Emmit Smith, Troy Aikman, Moose Johnson, and Deion Sanders. So to my great surprise, "Fourth and Long" came out this season starring Michael Irvin, and he has brought in a host of all time great players to help him pick one man for the Cowboys training camp. The group consists of prior candidates for the NFL that for one reason or another didn't make it. My husband, and I watch these second chance players battle out for a spot, and give it everything they have got. I have watched these men work to the point of throwing up on the field, and to the point of seeing their bodies break down. I watch in awe because I know I could not personally accomplish that type of work out. Although, I sat there last night watching the plays thinking to myself how this battle for Jude has been much like football. We are the key players that have lined up to go to battle for Jude, and to give our team everything we have. Without us being strong we will never make it through so despite our injuries we must brush ourselves off, and keep playing. We also have our defense, Offense, and Special teams geared up to take tackles, and blows for our baby. In the end of the game each day we are sometimes beaten up to the point we feel we cannot go on, but to win the spot we know we must. So therefore we ice ourselves down, we see our trainer, and we move forward to in the end win our superbowl for Jude!! I know that football players train hard for their roles in life, but we had no training regarding our baby having a stroke. It was unexpected, and we were unsure how to handle it. No one plans on anything ever happening to their child, but you just deal with it. We still get told, "I just couldn't handle having a disabled child". Sure you could, you have to, and you want to. You will do whatever it takes to protect and nurture your child. I also wondered if Jude would ever be able to love football as much as we do. We know we will never see him play in a pee wee game, but we currently help him participate in one of our favorite past times. My dad bought him a tiny Cowboys outfit, a bib to match, and a little bity Cowboys football to hold during the games.

I don't talk about this much, because I normally keep private that I was able to attend. My friend Dennis invited us to Michael Irvin's 2007 induction to the hall of fame party. I took my husband who said he was going to marry me three times for inviting him. We walked around the room sprinkled with sports greats of my early adulthood, and I was in awe. I was not star struck, but awe struck by the great players of my generation in all their glory. I shook Emmit's hand, and Michaels, and I went home a very happy girl!

Here are some pictures they took when we came through the door, and Emmit and myself

I was never able to watch a game in the old stadium, and with the rates in the new stadium I am not sure I will there either. Although, someday I would like to go, and I hope we can make that happen.

After we watched Fourth, and Long I gave Jude a 6 ounce bottle. He fought with me for a minute, and then took the entire bottle without stopping in about 4 minutes!! He then fell fast asleep, and slept through the whole night. I am hoping that we might be getting back on track, but again it's a roller coaster we ride with dips, and turns. I did talk to Jude's neurologist yesterday who confirmed that his lack of eating, and waking up at night can 100% be neurological. He informed me that we needed to watch Jude's weight, and if it started to decline they might look into a temporary G button for him. I do not want that to happen, and honestly I doubt it will. Jude is still gaining weight according to his last pediatrician visit. I have noticed that Jude is also getting a lot more phloem in his throat, but the good news is he coughs, and gets it out. I hope that this is an indication that he will have little problems with aspiration, but I am unsure if it is. I told Mike last night that I have noticed Jude looking directly at me a lot more. Before he would look at me, and seem to get a bit overwhelmed, and turn his head quickly. Now he really looks at me, and will even flash a little grin when he sees me. Another thing we have noticed is that Jude is turning his head to find voices, including turning to the left. He would not turn to the left before because that is his most affected side from the stroke. Jude is also working hard to keep his head up a lot more. Yesterday I found myself getting my hopes up that he will indeed eventually keep his head up, and maybe have a chance to walk. I am curious to know how long it took for other CP babies to learn to keep their head up, if they did. If you have any feedback I would appreciate it.

Thank you for indulging my long post today. I will leave you with some pics from last night.

A little better

Trying to feed Jude:





Not trying to feed Jude:





Trying to feed Jude:





Not trying to feed Jude:



You get the picture? He is actually doing better than he was, but he still resists eating at first. Last night I gave him some Tylenol, and he ate a bit, and slept well. So again, I think it's his teeth, and Jude is unsure how to communicate that they hurt. When I wasn't trying to feed him Jude was adorable last night, and very expressive, which made my day!

I was rather exasperated yesterday, and I appreciate everyone's words of encouragement. Once I left the busy office I called Jocalyn, and she went over some tips for ordering equipment. She even gave me the number to an office in Arlington that supplies adaptive aids. I then sounded off to her for about five minutes on keeping up with work, home, a disabled child, and more. It's nice to have someone that's can truly understand you. I also received a nice email from Gage's grandma who always gives nice virtual hugs. No one said this was going to be easy, but I am reminded to count my blessings. Jude giggles, he smiles, he coos, and he currently does not need any type of feeding device. Jude may have his issues, but he is overall doing much better than we ever expected him to, and that's what I need to focus on.

Last night I finished watching, "The Curious Case of Benjamen Button". Let's just say that my eyes are still swollen from crying at the end of that movie. I love movies that make you sit down, and think about your life, and what's important. This movie did a great job on displaying unconditional love. Mike asked me if I loved him that much, and I told him yes. I also bawled at the end when she was rocking the baby......if you have seen it, then you know what I am referencing. I was a red faced bawling sniffling mess.

Anyway, I have been trying to finish this blog since 8:30, and it's not 10:44 so I am super busy. Luckily, I have been on hold on the phone a lot, and able to finally complete this. Have a great day everyone.

A vacation in pictures

I am a bit overwhelmed today. Sometimes I feel like no matter how hard we try to deal with Jude's issues in a positive manner we get pulled into negativity. I am sure that it's lack of sleep again that's talking. Jude was up until 2:30 last night, and Mike was beyond frustrated so I took over. Sometimes I am not sure which direction to step to help Jude, and which direction to step to keep the rest of us sane too. Today I am looking into getting Jude a bath chair, a pediatric car seat, and he will eventually need an adaptive stroller. So the question is.......where do I find that stuff in DFW that accepts medicaid provided through MDCP. I also have personal insurance for Jude, but I believe this goes through MDCP. I get lost, and by not being at home I feel even more lost. I am sure if I was there for Jude's therapy I would know more about where I need to find items to help him. I am also setting up Jude's follow up vision screening with the pediatric opthamologist. In addition he still needs to see the pediatric hematologist. I can say that the reason for Jude's stroke is not relevant, but is actuality it is. #1. I need to know if Jude had any blood issues that could potentially lead to another stroke. #2. If there is something underlying (like my platelet issue) and if so, can this information help other children in the future? #3. Does he have any issues that need to be treated? I guess it's a pleothra of questions that need to be answered.

So it should be a week filled with appointments, and information. Jude ate pretty well while I was at home, but he is still resisting the bottle at first. He literally throws a hissy fit, pulls away from the bottle, and then will finally calm down and eat. You have to keep the bottle in his mouth until he gives up, and eats. Regarding baby food he will eat some of it, but only after he has acted like a sprinkler, and the feeder is coated in food. If anyone has had feeding issues like this before please let me know what you found out.

Jude will be one in September, and his next neurologist appointment is August. Since we will be approaching his first birthday we will be looking into a new EEG, and a new MRI. I am afraid they will have to put Jude asleep for the MRI, which scares me to death!!! I may request the MRI at cooks, and have the information sent to our doctor in Plano.

So without further delay here are all the pictures I promised.

Emily dropping off her smile boxes at Cook's Children's Medical Center:


Emily, and Jude at the zoo:


Emily, and Jude "watching" fireworks from her window:


Jude practicing keeping his head up:


So last night some of our friends came over Natalie, Andrew, and their daughter Camille. We had a great time talking, and they have been such huge supporters of Emily's Smile Boxes. We watched their little daughter play with Emily, and laugh herself silly. Em had such a great time playing with her, and "babysitting" her. Em was literally out of breath at one point, and looked at me saying, "wow babies are hard work". I just slightly grinned as I looked at Jude on the floor just laying there. He didn't do much. He didn't run around, giggle, sit up, or anything that Camille could. I felt sorry for him, and for us, but then shook it off as I picked him up. Jude looked into my eyes as I held him close, and it's like he could communicate with me. I believe that there is an instinctual nature for a mother to protect, and communicate with their child. I wished Em could share in more playful moments with him, but I know she loves him with all her heart. We were so happy they came over, and Camille took a liking to Jude's yellow chair. In fact any time I put Jude in there she would want us to get him out. Here is a picture of her telling Jude to get out,

It was sooooooooo cute!!! She is just precious. I truly enjoyed their company.

Fireworks are pending

I feel rather out of the loop since I have been on vacation. It's amazing how quickly the days go, and how you can lose track of news, and more.

Jude is doing well. He is frustrated because he is really wanting to hold his head up, but isn't able to. He is trying though, and I hope someday his body will cooperate with what he wants to do. I can really see the frustration in him that a normal stroke victim suffers from.

I am going to keep this blog short because I am working on a long blog. For awhile now I have needed to email the in utero MRI doctor who originally said she predicted Jude's outlook would be bleak. I needed to tell her that at only 19 weeks she was right in saying he suffered a bilateral bleed. There are many things I need to tell her, and I just need to find the right words. I am sure it will be a tear jerker for me so I am going to take my time. I will post it as soon as I get finished.

Before I got I would like to tell everyone how happy I am with Jude's new therapist Leah. I am afraid I cannot be here for his ECI meetings because of work. I am thrilled when I come home to new therapy items, instruction sheets, and words of encouragement from her. It's so nice to find someone that truly cares about Jude. Sometimes (not always) in the medical field the individual administering the therapy/diagnosis loses track that the child they are dealing with is indeed human. They begin to think of the baby, child, or adult as a stationary object, and lose track of why they went into the field. Luckily Leah, seems to have a genuine heart, and I like that!

Each year we can always see fireworks from the city's Independence day performance, outside Emily's window. This year I took Jude up to her bed so we could watch the brilliant display of color streaming across the summer sky. I stayed for a few minutes, and I noticed that Jude really didn't have any idea what was going on. I imagined him as a healthy 10 month old scooting across Emily's bed, and pulling himself up on the side to peer out the window. I smiled and gently kissed his head and fought back tears. I was thankful for him being in my arms, but I wished for more. As Ellen has frequently pointed out on her blog, it's okay to have moments like that some time. I have to remind myself that it's ok to cry every now and then...........it's okay!! The good news is we were all together as a family, and again we have a perfect view of wonderful fireworks from an air conditioned home. Smiles!

Have a wonderful, and safe fourth!!!

Still on "staycation"

While I am typing this I am watching Mike talk to Jude, while Jude sits in his yellow child rite. If you are just joining my blog, a child rite chair looks like a large version of a Bumbo. Jude cannot sit in a bumbo because it doesn't not provide enough support for him. His child rite chair gives him extra support, and also helps train Jude's abdominal muscles, and neck muscles. I am watching Jude look at Mike, Jude is making such progress about holding his head up. Now Emily just walked through the door with her friend Casen, and they are making Jude smile. Casen brought Uno so they are all going to play, and they have Jude included in the circle in the floor, which makes my heart smile.

Today on our "staycation" we took Em's friend Casen, and we went to see Ice Age 3 at the movie grille. This is a great little place near us where you can eat lunch, and watch a movie. Jude stayed with Mike's mom while we enjoyed the movie. He probably would have been okay at this movie, but I didn't want to overwhelm him besides his grandma loves time with him. I am enjoying my time home with my family, but I also stay in contact with my office by text/email. I am glad we stayed here for vacation it has saved money, and we are enjoying the time together.

I am happy to report that Jude is still eating better. I have noticed that he is eating solids better, and it's hard to get him to drink his formula. I have concluded this is Jude's way of trying to tell us he is ready to move to different levels of food. For awhile he quit eating the solid foods all together, but now he is wanting more solids, and limiting his formula. He is still eating about 20 ounces a day, and is adding in bananas with whole grain oatmeal, peas, and more rice. I am going to attempt to give him turkey, and sweet potato's later tonight. Slowly I will introduce more solids to him, and I am hoping he doesn't have any reactions. Jude's spasms were pretty frequent today, but we will not know a resolution for this until we see the neurologist again.

I cannot wait to post pictures for you guys from Emily's drop to Cooks. I think it will show how much work she is putting into her smile boxes. Anyway, I am going to run. Jude seems to be getting very frustrated watching them play UNO, it's almost like he wants to play. I know he doesn't full understand what they are doing, and is probably reacting to the noise. He is straining to look at the kids, and is trying to get their attention.

The zoo on a hot day

Today started my much needed staycation with my family. We slept until 9am (even Jude) and then we got up and headed out. We loaded up all of Emily's smile boxes for Cooks Children's Medical Center, and we dropped them off. Emily had so many boxes that they filled up the two level cart. I took lots of pictures, but I am afraid I left my card reader at work, so I will have to post them next week. The child life coordinator seemed very happy with them, and even invited Emily to a camp for kids who have ill siblings. I thought this was a wonderful gesture.

After the hospital we went to lunch, and then to the zoo. It was extremely hot but with shade, a lot of water, and misting fans we stayed cool. You could really see the difference between Jude's abilities, and other kids his age, but we still had a great time. We pointed all the animals out to Jude, and Emily really tried to involve him. At one point Emily wanted to go into a weather show that produced rain and snow on the audience, but I refrained from taking Jude. Mike went with Em, and confirmed that my suspension of over stimulation was probably right because another special needs child left in the middle of the show.

Jude is eating a bit better, and I even got 1/4 jar of peas down him along with his formula today. I am praying his eating continues to pick up. For some reason he is really resisting his bottle. The nutritionist is coming out next week, and I cannot wait to hear her suggestions.

Have a great day, and stay cool