We told Joseph that the tooth fairy was busy. I feel AWFUL! The good news? The tooth on the left is loose too. We will try and make sure he does not swallow this tooth too. Then John and I will have shot to get the tooth fairy to visit again. I think the tooth fairy has a lot to make sure for! I am sure she will leave money and a toy this time
Showing posts with label tooth fairy. Show all posts
Showing posts with label tooth fairy. Show all posts
Saturday, November 1, 2014
Joseph Loses His First Tooth - Finally!
Joseph FINALLY lost his first tooth! The boy is all most seven and FINALLY lost his FIRST tooth! His top teeth were pulled because he had fallen so much he had killed the root in those teeth plus cracked them. His bottom left tooth is the first tooth he lost on his own. The bad news... we think he swallowed it! :( Then to compound matters and make it worse... my husband and I forget to pick up his note explaining why is tooth was gone. So no visit from the tooth fairy. We are SO BAD!
Labels:
bad parents,
first tooth,
loss,
tooth,
tooth fairy
Saturday, February 22, 2014
I've Been Slacking!
I freely admit it that I have been slacking lately with keeping up with the blog. In my defense I have not been feeling very well. For the last four months I have not felt well and things have been getting worse. I have been complaining for the last year that my hair has been falling out and it is so bad not I can see my scalp through my bangs. I have been battling chronic anemia since the birth of the babies but I have no idea why. I take iron pills until I am good and a few months after I stopped I would be anemic again. So I went to my primary doctor and discussed with her my issues. She was not helpful because she told me to see a series of specialists. The dermatologist said it would not be something she could help me with. I have gone to a GI doctor. After being invaded in all sorts of ways that would make an alien abduction story sound tame the GI doctor determined I do not have issues with gluten, lactose, or have an ulcer. I thought I had an ulcer with all the symptoms I have including the chronic anemia. I was wrong. So what's my problem...why do I have the chronic anemia? So far, who knows? I also do not know what to think about my hair. So I have have several other appointments lined up. One with a hematologist and an endocrinologist. Hope to find an answer with someone.
As for the children. Well, they are far more interesting to talk about and I would guess that is why most people read the blog! Near Thanksgiving I had all the children lose at least one tooth. It was VERY cute. I love the picture I took of all of them smiling. Joseph has both of him front teeth missing. He had those pulled out when he was at the dentist in Las Vegas. Then Margaret has lost her left, top front tooth. James lost his top, left tooth that day! Very cute! Lots of smiles and not as much teeth! Thanksgiving was a nice time. We had moved into our new house near central Phoenix. I had Maddi, Dimitri and Jerrin all here at that time. It really was a nice Thanksgiving!
I will have to cover the children's 6th birthday some other time.
Christmas was a stressful time. We were running VERY low on money. I was back logged in bills and struggling to support everyone one in the house. My oldest son was helping out too. He had taken a part-time job at FedEx and was helping out with food and bills in the house. Jerrin soon left after Christmas. He went back home to the 16 year old he was seeing (he is 21). I cannot help but say what is in my heart...they do not belong together. Because of that I did not keep my mouth closed and told Jerrin what I thought. In doing so cost my relationship with him. If that is how things need to be right now then that is the case. It breaks my heart but I understand he is following his heart. I just cannot support in that endeavor at the moment.
New Years was quiet. John and I enjoyed our 14th wedding anniversary. It was nice to have a little time alone. By the end of January Maddi and Dimitri had moved out. I hated to see them go. I really did. John and Dimitri were seeming to argue or have some sort of issue most every day. I honest think John was the cause of a lot of the issues. I don't think he meant to be but subconsciously I think he wanted to have the house to himself. After Maddi and Dimitri left John and I were coasting along but things were tense.
We were finally able to find someone to do rehab.services for the Margaret and Joseph. We also found someone to give us some respite. So in the 18 months I have been here I have only been successful in getting rehab. services and some respite set up along with a little intermittent physical therapy services. My children need so many other therapy services and I just cannot find service providers here. Just getting into some doctors too can be a chore. I have been trusting John to handle those duties and I have been trying not to interfere but it is getting harder. I know I need to get the children in to see doctors and specialists and the time is running out for me to have "good" insurance and the appointments are SO far out into the future!
My time is running out because I think the plan is for us to return to Las Vegas. John and I both like it there more. I can get the therapy services I need for the children easier. The therapy services, especially at this age, is significantly more important than them seeing doctors. I know Joseph is a medical mystery. We are still at a lost. In Joseph's recent deep muscle biopsy test and lumbar puncture we still did not find answers. Joseph's test from the lumbar puncture did not show cerebral folate deficiency. That was good news. In the muscle biopsy test on the other hand did not show me what I wanted. The purpose of the muscle biopsy was to test for some of the more "common" forms of mitochondrial disease. Oh course, Joseph tested negative for all of those. That does not mean there was nothing found that was unusual in his biopsy! Joseph showed an increase in positivity for acid phosphatase and he showed abnormal storage of lipids (fats) in his muscle tissue. Not enough for the pathologist to be able to diagnose a specific disease but enough for it to abnormal. In the end the pathologist said he could not exclude mitochondrial disease (because there are other forms that cannot be tested but are determined by ruling out other diseases) but said Joseph should be examined for an "unspecific" (the pathologist's word and it means he could not point to any one disease because Joseph's symptoms were not severe enough) metabolic disease and genetic testing. Ironically, I have done the genetic testing. Nothing was found there. That does not mean I would not revisit the genetic testing again. Tests do change and improve. Metabolic disease on the other hand is not something we have thoroughly investigated. Joseph has had abnormal blood work that points to possible metabolic disease but it has never been to the level that a doctor could point to some number and say....hum, looks like we have a problem with so-and-so disease.
I cannot state how frustrating it is to know something is wrong with your child. You fight years and years to get specialist to see your child as something more than just a preemie that is having problems. Once I finally got to Phoenix...that happened. I have specialists here that agree with me. Something is wrong with Joseph. As to what that is, it even has the specialists here stumped. All I want is to know what is wrong and if there is anything I can do to help Joseph reach his maximum potential.
Sigh, okay, enough venting about Joseph and his team of doctors.
John and I had a really nice Valentine's Day. We got to go out on a real date and have a nice time. I was worried that things would not go well for us since I knew there were relationship issues we had to discuss but we had such a nice time. We did not do the things we wanted to on Valentine's Day because the relationship stuff turned out to be a HUGE topic and pretty productive discussion overall. Currently John and I feel closer to each other than we have in years. I am happy right now and so is he. I wasn't sure if we could have happiness like that again but it seems like we can. I think it has been helpful to have all the twenty-somethings I had in my house gone. This has allowed John and I to be more ourselves. To have our time alone in the evening and the space to fight (and/or make up...LOL) as we wish is rather priceless.
Okay, now that I am caught up I will work on keeping the blog more up to date. Having a desktop really motivates me to write!
![]() |
Thanksgiving Day 2013 |
I will have to cover the children's 6th birthday some other time.
Christmas was a stressful time. We were running VERY low on money. I was back logged in bills and struggling to support everyone one in the house. My oldest son was helping out too. He had taken a part-time job at FedEx and was helping out with food and bills in the house. Jerrin soon left after Christmas. He went back home to the 16 year old he was seeing (he is 21). I cannot help but say what is in my heart...they do not belong together. Because of that I did not keep my mouth closed and told Jerrin what I thought. In doing so cost my relationship with him. If that is how things need to be right now then that is the case. It breaks my heart but I understand he is following his heart. I just cannot support in that endeavor at the moment.
New Years was quiet. John and I enjoyed our 14th wedding anniversary. It was nice to have a little time alone. By the end of January Maddi and Dimitri had moved out. I hated to see them go. I really did. John and Dimitri were seeming to argue or have some sort of issue most every day. I honest think John was the cause of a lot of the issues. I don't think he meant to be but subconsciously I think he wanted to have the house to himself. After Maddi and Dimitri left John and I were coasting along but things were tense.
We were finally able to find someone to do rehab.services for the Margaret and Joseph. We also found someone to give us some respite. So in the 18 months I have been here I have only been successful in getting rehab. services and some respite set up along with a little intermittent physical therapy services. My children need so many other therapy services and I just cannot find service providers here. Just getting into some doctors too can be a chore. I have been trusting John to handle those duties and I have been trying not to interfere but it is getting harder. I know I need to get the children in to see doctors and specialists and the time is running out for me to have "good" insurance and the appointments are SO far out into the future!
My time is running out because I think the plan is for us to return to Las Vegas. John and I both like it there more. I can get the therapy services I need for the children easier. The therapy services, especially at this age, is significantly more important than them seeing doctors. I know Joseph is a medical mystery. We are still at a lost. In Joseph's recent deep muscle biopsy test and lumbar puncture we still did not find answers. Joseph's test from the lumbar puncture did not show cerebral folate deficiency. That was good news. In the muscle biopsy test on the other hand did not show me what I wanted. The purpose of the muscle biopsy was to test for some of the more "common" forms of mitochondrial disease. Oh course, Joseph tested negative for all of those. That does not mean there was nothing found that was unusual in his biopsy! Joseph showed an increase in positivity for acid phosphatase and he showed abnormal storage of lipids (fats) in his muscle tissue. Not enough for the pathologist to be able to diagnose a specific disease but enough for it to abnormal. In the end the pathologist said he could not exclude mitochondrial disease (because there are other forms that cannot be tested but are determined by ruling out other diseases) but said Joseph should be examined for an "unspecific" (the pathologist's word and it means he could not point to any one disease because Joseph's symptoms were not severe enough) metabolic disease and genetic testing. Ironically, I have done the genetic testing. Nothing was found there. That does not mean I would not revisit the genetic testing again. Tests do change and improve. Metabolic disease on the other hand is not something we have thoroughly investigated. Joseph has had abnormal blood work that points to possible metabolic disease but it has never been to the level that a doctor could point to some number and say....hum, looks like we have a problem with so-and-so disease.
I cannot state how frustrating it is to know something is wrong with your child. You fight years and years to get specialist to see your child as something more than just a preemie that is having problems. Once I finally got to Phoenix...that happened. I have specialists here that agree with me. Something is wrong with Joseph. As to what that is, it even has the specialists here stumped. All I want is to know what is wrong and if there is anything I can do to help Joseph reach his maximum potential.
Sigh, okay, enough venting about Joseph and his team of doctors.
John and I had a really nice Valentine's Day. We got to go out on a real date and have a nice time. I was worried that things would not go well for us since I knew there were relationship issues we had to discuss but we had such a nice time. We did not do the things we wanted to on Valentine's Day because the relationship stuff turned out to be a HUGE topic and pretty productive discussion overall. Currently John and I feel closer to each other than we have in years. I am happy right now and so is he. I wasn't sure if we could have happiness like that again but it seems like we can. I think it has been helpful to have all the twenty-somethings I had in my house gone. This has allowed John and I to be more ourselves. To have our time alone in the evening and the space to fight (and/or make up...LOL) as we wish is rather priceless.
Okay, now that I am caught up I will work on keeping the blog more up to date. Having a desktop really motivates me to write!
Labels:
GI doctor,
Lost tooth,
mitochondrial disease,
money,
Phoenix,
respite,
slacking,
son in relationship I can't stand,
stress,
Thanksgiving,
tooth fairy,
unspecific metabolic disease,
Valentine's Day
Thursday, March 21, 2013
Where did the last month go???
![]() |
Photo Credit: Chasedumont.com |
So let me give a brief run down on what all has been happening.
February 12 - I took the kids to a pediatrician. He is new to us and we had a great visit. I am happy we went there. As I have gone around to other specialists they know the new pediatrician and say he is a great guy. How is that for giving you confidence in your primary care doctor!
February 15 - John came to Phoenix for the weekend. We are working hard at re-building our relationship. I am hoping it can happen (for our sake and the kids).
February 19 - Joseph went to the Melmed center to be evaluated. Dr. Melmed examined Joseph and said he may be labeled as autistic. He would need additional psychological testing. It really saddens me to hear this. Mostly because that is not what I think is wrong with Joseph. To me autism is a list of symptoms of a disease. I want to know the disease (root cause) on what is going on with my baby. I am glad of all the improvements Joseph has made in the last year and a half but I would say he is now, at least linguistally, where Margaret was two years ago. I am hoping he will continue to rapidly improve with his speech. I have contacted a psychologist to do the additional testing. I am waiting to hear back from their office.
February 28 - We finally got to see the ENT. I was FURIOUS at first with the doctor's office. I had gotten a call the day before and I asked them if they had received all the information for the Margaret and Joseph to be seen the next day. I was told yes. I had spent an hour in the office last time filling out paperwork and medical releases for them on Feb. 6. The day of the appointment I was called at about 10am. The nurse asked about Joseph's surgery. I said he did have surgery but I did not have the records handy. They were at the hospital and I did not remember any of the details because this surgery happened back before Joseph turned one. The nurse then tells me the doctor will have to have the records and Joseph would not be sent that day. I was LIVID! Here I was having the appointment cancelled on me at the last minute. I got snippy with the nurse but I ended the call very politely. It completely took her off guard because I KNOW that was NOT how she was expecting the phone call the end....LOL. About an hour later I had the ENT doctor call me. He said he wanted to discuss Joseph and would I please call him. He said he was out at the hospital on an emergency and gave me his PERSONAL cell phone number. I was shocked! Every bad thought I was having I lost at that moment. I called the ENT back and spoke to him. I explained about Joseph and why I wanted to bring him in. The ENT agreed with me and said he was looking forward to seeing Joseph this afternoon. I told him his office staff had cancelled Joseph's appointment. He said there was no need for that and to bring him in. He said he was going to call his staff and tell them to put Joseph back on the books. We went to the appointment. I took everyone with me. I had me, Bailey and Alexa along with all three children. In the waiting area James decided to misbehave so I had Alexa take him back to the van for a bit. I know he screamed like a banshee but he did finally calm down. He was able to rejoin us before we went back to the exam room. While there the James was having a fit. He wanted to see the doctor too. Plus Bailey had told him he would get shot if he had to see the doctor...you know what, James agreed. This is the danger to threatening James with something you can carry through. He takes things so literally and he would expect you to carry though with what you promise. He would NOT let it go! When the ENT came in James INSISTED he get a shot. The doctor tried really had to humor him. The fact he took the time to do that made me like the guy! He brought in suckers in the end and James was at least distracted for a bit. We started to talk about Joseph. I explained all that was going on with Joseph and the multiple health issues he was having. Bailey piped in and said I did not believe in vaccinating the children or giving them medication. I explain why to the doctor since he had asked about giving Joseph the flu shot vaccination. When I was done he turned to Bailey and said it was a good thing I was not giving the vaccinations or medication consider all that is going on with Joseph and there are still a lot of unanswered questions. So the ENT examined Joseph and Margaret while we discussed Margaret. Margaret was found to have enlarged adenoids and inflamed sinuses. We are going to treat her with medication at the minute since the only other real option is surgery. I have no interest in having her go through surgery at the moment. I had also given the ENT a list of all the specialists we had seen in Las Vegas. The doctor was nice enough to recommend local doctors for each of the specialties. That was SUPER nice! He is a really great man and I can tell he care a lot about the children. What more can you ask for in a doctor?
March 8th - I get a notice from my insurance about the visit from the Melmed Center for Joseph. I had checked and there was not a problem. The insurance comes back though and says that the Melmed Center is out-of-network and I about nearly panic! The bill is for $660! I cancelled my appointment for Margaret (since it was for the March 13th) because I panicked! I wanted to make sure the medical insurance was going to cover the bill. It took several days and several phone calls but we finally think we have it straightened out. At least the insurance admitted there was a billing error on their part.
March 12th - I called the Geneticist's office. OMG, I wait on the phone for someone to pick up for 40 minutes! I get through and give them information. I find out they are booking appointments into October at the moment. Not shocked but I was hoping for better. They would not schedule an appointment for me until I fill out all the new patient paperwork. I got the stack in a few days ago...WOW! So I will be working on this information so I can fax it in and set an appointment.
![]() |
You can see the height difference in the boys. It's a lot! |
March 18th - Finally got someone from the Long-term care people call me. They supply the funding for the services I could get the children (such as therapies (OT, PT and ect) along with anything else) through the DDD. I tried to do this before but I could not. I am hopefully I will be able to get it done this time. Got the ball rolling again at least.
![]() |
Happy Birthday Bill! |
That evening we celebrated Bill's birthday! The kids were SO excited! They LOVED eating cake and seeing the candle blown out. I am glad they had fun!
![]() |
My Baby lost her first tooth! |
March 20th - Mark it on your calendars...Margaret lost her first baby tooth and she is the first of the babies to lose ANY baby tooth on their own (Joseph has his two top teeth pulled awhile ago). I cannot believe she lost her tooth. I am glad she did though. She had her permanent tooth emerging in the floor of her mouth. It looks HUGE compare to the baby teeth. I am hoping the tooth will move forward on its own but I am worried it may not. Will be making an appointment for her to go to the dentist. I got to help play tooth fairy. I had found a small Hello Kitty bag with a toothbrush, toothpaste and dental floss. I put that under her pillow along with a dollar bill. I also placed a dollar bill under the boy's pillows. I did not want them to get it into their head that they had to get a tooth out to get something from the tooth fairy too. In the end the money meant nothing to the children...everyone fought over the Hello Kitty stuff...LOL!

March 27th and 28th - James and Margaret have an appointment with the dentist. They will go first and the next day Joseph will go. It will be good to take them in and have them examined.
Now you are caught up on at least part of what has been going on. I have been SO busy with work and other things too. At least I have been able to get things squared away though. In getting all of this off my mind it leaves me free to think about other things and do write the stuff I need to for work.....Thank goodness! Got to get a paper researched for school and then one written for work. Back to work for me...
Labels:
cerebral folate deficiency (CFD),
DDD,
developmental pediatrician,
endocrinologist,
ENT,
geneticist,
lost first baby tooth,
Melmed Center,
mitochondrial disease,
Pediatrician,
therapy,
tooth fairy,
work
Subscribe to:
Posts (Atom)