So, it was back to school and kindy today !!
I always look forward to the school holidays when we can have a week or so together. It’s much more fun than my wife leaving early like she does and then I taking the kids where they need to be. Pretty enjoyable holidays as usual. The 2nd week always seems to go quicker than the first. Once the holidays have come to an end I’m kinda ready to carry on.
So, my daughter will be at school next year, so I’m very excited. It will be good no longer having the 10-15 minute walk to kindy. She still travels in the push- chair which she will do until she is finished there. We walk home after kindy. Next year it will be just down the street for both of them. School is only a few hundred metres away. Not even 5 minutes walk.
I’m often getting asked what I will be doing with myself, how I will full in my time. Not 100 % sure yet. My goal is to work from home. I’m slowly making progress with my online businesses. We’ll reaccess things at the end of the year.
My Epilepsy carries on. Looks like I have had about 7 episodes in the last month. That’s probably a bit of an increase. There was a stage I was having 2-3 a month, maybe 4. So, who knows why.
Most of these turns continue to be brought on by emotions. For example, yesterday we had friends for lunch. When they were about due to arrive, I heard a knock at the door. So, I went to open it…….But it turns out it was my son. He thought it was funny to pretend someone was there. Our friends may have arrived pretty soon after that. I must have gone and had a sleep. When I came out I didn’t really have much to say. It took me a while to get back to myself.
There still isn’t much progress when it come to the NZ Epilepsy Foundation. I actually missed last months meeting, but I will be going to this months in a couple of days.
So, 10 more weeks of school…..
What do you think of the photo ? Not bad for a 7 year old !!
The All Blacks ( New Zealand Rugby Team) recently visited kids in hospital with Epilepsy. This was great to see on our 6pm news, especially when it was on Daffodil Day here in New Zealand. Daffodil Day symbolises hope for 1 in 3 New Zealanders affected by Cancer. Of course my heart goes out to anyone affected by Cancer, but it does receive alot of attention compared to Epilepsy.
Sometimes here in NZ it seems like the world revolves around the All Blacks…..or at least the media see it that way. So to have them visiting Kids with Epilepsy was very pleasing.
( click the pic below to see a short video )
Most Children with Epilepsy should be able to attend normal mainstream schools. They should be able to take part in all activities. As long as the school is informed of the Epilepsy. I remember in my school days there were a few things I wasn’t allowed to take part in, which was a little bit silly. I was quite capable. There was a teacher or 2 that were quite aggressive. Because of a lack of understanding, one thought I was just messing around. At Polytech ( Tertiary Education), I studied Landscape Design. We did alot things in gardening, such as spraying. I was never allowed to do that. Once again, it seemed silly. I come from a Dairy farming family and I was very active on the farm. I had my own motorbike from a young age.
Its may be a good idea to involve other children in ones Epilepsy as well. How ? Well, If they are told about ones Epilepsy, they can learn what to do when a seizure occurs. It will show the children that there is no reason to be scared or panic.
There may be some that won’t be able to attend school. This may be the case if they have many seizures. When I hear of people that have many seizures a day, I think about how lucky I am. Some children may have additional problems. Maybe their Epilepsy leads to learning or physical difficulties. Many children these days seem to have learning issues. I sometimes wonder how real it all is. These sort of issues weren’t as common when I was at school.
My education was effected by my Epilepsy. When it arrived , I was 13-14. I had a few side effects such as gaining weight and tiredness. That’s funny, because since then I have had opposite effects. I have felt that I can really eat anything and not gain weight. I still try to not eat to much junk. Also with the sleeping. I’m not the best of sleepers. I’m often asleep in front of the T.V at 7pm, but only end up spending 3-4 hours in bed. HABIT , HABIT, HABIT. Alot of this is due to bad habits. There have been times that I have improved my sleeping. But then I go back to bad habits.
So, I am still very motivated to get Epilepsy out in the public. We need to get more people understanding it. I won’t stop until I am part of achieving this.
Most people experience a sense of shock, fear and panic when seeing a seizure for the first time. That is completely understandable.
Many people have very little understanding of Epilepsy… well, that’s what I have found. The best thing to do is offer moral support.
So, as you may know,a person having a Tonic – Clonic / Grand Mal Seizure should be laid on their side. This is once any convulsions have stopped. Something soft should be put under their head. Nothing SHOULD EVER be put in ones mouth when having a seizure.
Is it worth calling an Ambulance ? If people understand the Epilepsy, it may not be required. This is something that has been frustrating over the years for myself. I now pay an annual membership fee to St John ( NZ Ambulance Service ). It is $80 a year and this covers our whole family. It’s very much worth it , because if you aren’t a member and receive their service, you are charged MORE THAN $80. I can’t recall exactly what it is.
It is important to make sure the history of what happened is recorded. Personally, I write about every seizure I have.
What happened ?
Why did it happen ?
Where did it happen ?
By keeping record of my seizures / turns , I can see whether my number of turns is increasing or decreasing. It’s always interesting to count them once we reach the end of the month. It seems like my turns have increased a wee bit over the last 12 months.
We must remember that there are other conditions that cause a person to have a seizure like episode. Perhaps someone may jerk and twitch, fall down or lose consciousness.This isn’t necessarily Epilepsy. The likes of an E.E.G / Scans looks further into this. All the Scans , etc , that I have ever had have never shown an reason for my Epilepsy.
BUT HEY !!! LIFE GOES ON !!!
Well, it’s been a while since I have posted. I guess the days just continue to fly by. My days are all pretty much the same. Nothing that exciting.
My Epilepsy hasn’t been to bad lately, but perhaps it was better 12 – 18 months ago. It’s probably 12 months ago that I stopped taking Topriamate. I had 5 turns/ seizures during May and 6 in April. I’m still going to stick to my Magnesium. Who knows whether it’s having any sort of effect. There is no stand out effect at this stage. Magnesium is good for you, so………why not.
Remember I had talked about our Epilepsy Family Fun Day ? Well that never happened 😦 A couple of the people on our board had health issues at the time, so I think that made some of the organisation difficult.But the biggest thing that continues to be the issue is people. Where are people with Epilepsy ? Most seem to be to shy. Maybe that is understandable, but I don’t feel that way. As I always say, of course I would lose my Epilepsy tomorrow if I could. Who wouldn’t !! But, it’s really exciting to think I could be involved in getting Epilepsy to a better place than it currently is.
It’s been really rainy here in the last week or so. I have had to endure the rain when getting the kids to school and kindy a few times. No one likes walking in wet shoes and clothes. I wore my gumboots this morning !!! A bit heavier, but certainly drier.
Just one more week to go of this school term !! Isn’t it scary to think we are half way through the year !!
Well, I guess I don’t really have much more to say…..sorry. None of that was really that exciting was it.
Until next time !!
That’s right, come out come out wherever you are !!!!
“Why” ? you may ask. Because people with Epilepsy can achieve alot more together. There are other people with Epilepsy out there. How much of a group do you have in our area, town , city ?
This is something we really struggle with. Let’s do the Maths. Here in Hamilton, we have a population of 150,000. Let’s say 1% of them have Epilepsy in their life. That’s 1500 people !!!!! That’s alot of people. Let’s scale it down. What about 1000 people, or even 500. Those are big numbers. Surely some of those people would like to be part of something. Think of it as a club, community, group…whatever you want to call it. We all have something in common. Yes, it’s something we would rather be without, but why not try and make the best of it.
There are many ways we make friends. Maybe you met your friends through education, such as University or School. Maybe you worked together. Maybe you played sport together. We make friends through our children as well. We have made some of our best friends through starting a family !!!
Forget about embarrassment. There is nothing to be embarrassed about. There are others out there with Epilepsy. That’s why it makes so much sense not to be embarrassed. I’m proud to say I don’t feel embarrassment about anything really. Perhaps this is because of my Epilepsy.I think it has made me stronger in a way. Yes, I like to be my best and make a good impression. We should always try and be our best. But, I try not to sweat the small stuff. I don’t care what others think of me. People out there don’t know your story, don’t know what you are doing with your life.
Remember your younger years ? Did you get called silly names ? Did you want to be one of the cool kids ? When we get older we realize how silly all of that was. If only I could have known what I know now 20 years ago.
We have made some ground here in New Zealand… we are slowly getting some events for people with Epilepsy in place. We still have a long way to go, but it is very encouraging. I’m very proud and excited to be part of it.
So please …..come out, come out wherever you are !!!!
Do you like my t-shirt ?
I’m not afraid to wear it out !!!
When we live with Epilepsy, we have to be positive.
Sometimes it may be hard, but remember that things could be worse. Think of all the good things in your life. Stay active. Don’t think you can’t do it because of Epilepsy. Epilepsy can be your motivation.
Remember….Our Aspirations Are Our Possibilities !!!!!
As I have said many times, it’s important everyone with Epilepsy realizes they are not the only ones .They are not alone.There are others out there, so there is no need to feel embarrassed, or like a “weirdo”.
Continue reading “Get Together With Our Epilepsy”
Today has been one of those days. You know , right ?
What I mean is a day when things aren’t much fun, you look forward to when the day is over. I felt a bit frustrated this morning. The usual bit of silliness that happens when the kids are having breakfast. My wife leaves just after 7 in the mornings, so it’s just me when the kids are eating. I often tell them to stop mucking around and eat their breakfast. They complain that the other is looking at them !! CRAZY KIDS !!!
Continue reading “Not the best of days…”
Have you ever heard of Magnesium as a treatment for Epilepsy ?
Doing a google search, I see that there are a few articles / bit of info about Magnesium and Epilepsy. One would have to have a chat with the doctor first before they jumped in boots and all. But if you were to eat a few foods high in Magnesium, I don’t really see the harm. There is a difference between what we are eating and the medication we are taking. Our eating is a way to keep it all natural.
Continue reading “Magnesium & Epilepsy”
So, Medic Alert ….
Medic Alert is a way your information is kept about your health issue. You wear a wristband / bracelet or something around your neck. On there is what health issue you have, plus a pin number. Do you have something like this where ever you live in this big wide world ?
So say something happens and you end up in the arms of Medical staff, they can look at Medic Alert and see why whatever happened may have happened. Perhaps they will discover there are some drugs you can’t take. I know a few people that wear Medic Alert for this reason. Of course, mine is for my Epilepsy. One thing we haven’t done is kept my info up to date. I should go through my doctor and get things signed off. This would be what medication I take, etc. My medication has changed many times over the years.
I always wear mine around my neck. I have worn a wrist band a few times, but it annoys me a bit. I guess it is something you’d get used to.
I recently received an email from Medic Alert. They were asking me to fill in a survey about my experiences . The main question was whether I had had any experience of medical staff missing my Medic Alert / not taking notice of it. This has happened to me several times.
I had a seizure ( turn) one day when I was picking my son up from school. Even though I probably would have been fine, some thought I was having a heart attack. So, the Ambulance arrived. Did they see my Medic Alert around my neck ? NO !! Don’t you think they should have looked for it ?
So from the look of the survey, it sounds like there has been other people go through this. We pay a yearly fee for my family to be covered for Emergency services like this. I think we pay about $90 a year. Without this , it would pretty much cost that for using their services just once. So it’s good it covers all 4 of us.
Our Ambulance service comes from St John . They rely heavily on donations/ fundraising from the public. Perhaps the government could assist them a bit more.
I’ll say it again. There is a need for a better understanding of Epilepsy.
It’s not really that hard. It’s like alot of things.
TALK ABOUT IT !!
ANSWER QUESTIONS !!
ASK QUESTIONS !!
DON’T BE SHY !!
As we know, the public really lack understanding. Everyone is different , just like our personalities. Imagine a world where everyone is the same. Maybe that will happen one day. Not quite everyone… but a few. All the talk of things Genetic’s. Imagine picking what sort of child you wanted to have. That’s sick !! If you were able to pick what colored eyes and hair your child was to have… If we get to that stage, we would have seriously lost the plot.
ANYWAY, SORRY ABOUT THAT…
Back to the subject.
So, why do Seizures arrive ? Do they come when you are in certain situations ? When your tired or stressed ? These types of things create brain activity.
I keep a diary of my seizures or “turns”. I can often feel when they are coming.Can you predict when they are going to happen ? I wonder whether predicting them and telling my wife about it stops them from arriving. I always ask Alie ( wife ) what happened. I sometimes feel like I’m trying to gain attention…well, I sometimes think that is what she may be thinking. But, it’s all for my diary. That info is handy when you go and see the Doctor or Neurologist.
I’m super excited been involved in the NZ Epilepsy Foundation. I also run a Facebook page for my area. We may soon get some names of people who have Epilepsy. This will help us get a bigger group together.
I’m very glad Hayden ( son ) really understands Epilepsy. He’ll be 7 in May. A couple of days ago we were walking home from school and and he kept asking me if I was ok. This was because I was repeating what I had said. I was fine. We’ll have to get Claudia to that level of understanding in the next few years . She’ll be at school next year.
They need to know –
* What Epilepsy is
* What happens
* Why it happens
* What to do
Encourage questions !!
I love to Exercise. I have never driven so I walk a few KM’s every day.I’ll be going for an hours walk tonight. It’s time-out with music in my ears. It helps with Self-Esteem as well. I have looked to getting involved in some social /activity groups. This is where a license would be handy. I use the bus service, but I have to consider where these meetings are and whether a bus is going there. It’s not the best idea to be relying on public transport late in the evening.But, life goes on.
This was a fairly random post about a few things wasn’t it. It was just a time to get a few things off my chest.
Have a good weekend !!!
Have you or someone you know with Epilepsy had trouble with Employment ?
This is something that really bothers me. At a recent seminar, a Neurologist said that Employers shouldn’t fear Epilepsy. He said that anyone could have a heart attack at anytime….and Employers aren’t concerned about that. He said this with a bit of a grin on his face though 🙂
Maybe employers feel that your performance won’t be up to the same level as others. Maybe they fear you are dangerous or perhaps you won’t be able to deal with the public.
We all have our place in society. The public very much lack knowledge of Epilepsy. It gets no time in the media. Sometimes it feels like some health issues such as Cancer receive far too much.
My heart goes out to anyone with any health problems.
There shouldn’t be to much difference between a employee with Epilepsy and one without. Personally , I think my 20 years with Epilepsy has perhaps made me more determined.
How often is one effected by their Epilepsy ? How often and how severe are their seizures ? Currently I have been Epilepsy free for 2 weeks. So, 99 % of the time I am fine. I have been a Stay At Home Parent over the last 7 years and we have never had any problems.
If you find an employer that is understanding of your Epilesy and how it works , then all systems should be GO !!
If you have the qualification’s , you should be looked at the same as the next candidate. One of the best things you can have on your C.V is a good attitude. Do you have it ?
My daughter will start school at the beginning of next year. I may look to some more tertiary study , but my aspirations lie in home business. Hindsight would have been handy all those years ago when I went through Tertiary Studies. We always thought my Epilepsy would go away with time. If I had known it would still be around after all these years , I may have studied something different. I studied Landscape Design. There can be some physical work involved there and a drivers license would be needed. My interests are very much in front of a computer these days.
ONWARDS AND UPWARDS !!!
Hope you had a fantastic Christmas. I had a pretty good one. It’s hard to believe that it was 2 weeks ago. Time goes to quickly. There are times when that’s a good thing, but there are also times I wish it would slow down. For example, I was looking forward to the school year ending, meaning more family time. But , before we know it January will be gone and everyone will be back to school. I enjoy the holidays because of Alie ( my wife ) being a teacher.
So, a little while ago there was a very interesting story on the news. This was about a mother who was taking Epilim while pregnant and wasn’t informed of the issues it leads to. Her teenage daughters have had some development problems.
People are very unaware of this. I recently learned about this at The Brain Train. The Brain Train was an Epilepsy Meeting with a few knowledgeable guest. One of them was from FACSNZ which stands for Foetal Anti -Convulsant New Zealand. She told us how many drugs can have a real effect on a pregnant woman, leading to their babies / children. It seems not many know about this. But,it is a topic in different places online.
There was a reaction to this news story on Facebook. Many people seemed to think they were an experts. This is the same whenever it comes to Epilepsy. Frustrating !!
Take a look at the news story – HERE
I have gotten to know Roxanne because we have something in common, which is Epilepsy. She is very active online when it comes to Epilepsy and this very much benefits others. People like Roxanne is just what Epilepsy needs.
Take a look at her blog – “SEIZE”URE THE DAY!
I didn’t consider myself an EPILEPSY ADVOCATE until after I had an unexpected seizure while I was driving. I had been seizure free for seven years. The drug store that filled my prescription switched the company that manufactured the generic medicine I took because it was cheaper for them. After taking that different generic medicine one day, I had that car wreck. My seizure wasn’t like my usual stare for thirty seconds. This time I stiffened up, fought my daughter while she tried to take over the steering wheel and pull the emergency brake, and my foot stayed on the gas pedal.
I don’t remember anything. I don’t remember hitting multiple mailboxes, swerving side to side on the road, and then hitting a tree. Thank goodness the tree went in between me and my daughter. I didn’t come out of my seizure until someone was pecking on my car door window. Then I noticed someone else carrying my daughter from the car to lie her down on the ground. My other daughter in the back seat was little and had to be in a car seat. Thank goodness she was restrained and didn’t have any cuts or bruises. My oldest daughter’s ankle was shattered! She has had five surgeries in the past 6 years. Finally her ankle had to be fused with titanium. I’m not blamed for the wreck, every time someone asks what happened to her ankle she just says “I was in a car wreck”. Never once have I heard her say that I did that.
While she was out of school, I wrote my Congressman and fought my insurance company about taking generic epilepsy medicine. I WON! Brand name medicine is what the doctor orders for me now. I don’t drive though. I found a way to deal with that. Since I can’t make it to epilepsy group meetings because I don’t drive anymore, I can talk to people on line. Meeting people from everywhere!
Something I am doing now that I never thought I would do, WRITE. I used to work in the medical field and would talk to patients about epilepsy. Now that I am not working, it’s amazing at how many more people I have talked to.
Spreading EPILEPSY AWARENESS is what I do now.
The number of overweight youngsters has increased dramatically over the last thirty years. Obesity has currently surpassed smoking as a pathological state. If action is not taken,Obesity is probably going to continue throughout lives. We do not want our kids to be having shorter lives than ourselves. After we scrutinize technology, it’s as if it’ll be the opposite. Ones on the improve , and the other is going down hill.
Obesity will bring several issues like Diabetes and Cancer.
So, what steps ought to be taken ? Is Education the solution ?
Parents have to take a look and see that everything we eat has an impact.
Education is a component of the solution, however alot more can be done. A part of the answer for Smoking has been the adding of a tax, which means higher costs. This could be a deterrent from purchasing some food . Some countries have goals of been smoke-free by an exact date. Sound Optimistic ? New Zealand goal is to be smoke free by 2025. It seems like a big ask, but smoking continues to decline. We all know that setting goals is the best way to reach targets. More information needs to be in place within the food market and on food packaging. This can lead to better decisions.
At times it looks as if Government is bringing up children, not parents. Parents need to be responsible when feeding their children. Parents are of course the biggest influence in a child’s early years. Habits can last a life time.
Children are not as active as they were in the past. Technology has modified the way many spend their time. How much time do your youngsters spend on the computer or with a tablet. Look at activities 30 years ago. Everyone was taking part in a lot more sport and generally just more active. Sport could be made more accessible, fees could be brought down.
Tackling Obesity may begin as early as in the womb.
At what level is the mother-to-be weight at ?
How much weight should she gain throughout gestation ?
Should she be eating additional food for her baby ?
How long should breast feeding last ?
Everyone needs to be eating their fruit and vegetables. How often do you have takeaway’s ?
Advertising is part of the problem. Adverts need to be limited and also at the right times. In some countries, Alcohol has been taken away from the television screen. Maybe the same action could be taken for some foods. EG : McDonald’s.
When you see that McDonald’s advert, do you desire a Big-Mac ?
It’s up to individuals to make the right decisions. Are you making the best ones ?
What is that you may be thinking ..
FACS can occur when anti-convulant Medication is taken during pregnancy. The medication crosses the Placenta and through to the developing Fetus.
FACSs refers to 3 different syndromes. These are –
- Foetal Valproate Syndrome
- Foetal Carbamazepine Syndrome
- Foetal Hydantoin Syndrome
FACS can be diagnosed by a specialist when a mother to be is taking Anti – Epilepsy Medication during pregnancy.
The of type of drugs to think about are –
- Tegretol – Carbamazepine
- Dilantin – Phenytoin
Some of the possibilities are
- Spina Bifida
- Visual Difficulties
- Lower IQ
- Small size at birth
- Attention and Memory problems
- Slow Development
I have seen many questions about Medication and Epilepsy. It was interesting to hear this information. I have always thought the possibilities of these type of problems due to Epilepsy were pretty small. As I said, not all woman taking this type of medication will be affected, but sounds like they are a possibility.
I have often though that it wasn’t anything to worry about. I did think about this sort of thing when becoming a father. I was glad we didn’t have any problems getting pregnant. We have 2 healthy children.
People can be on these drugs for types for Medical issues other than Epilepsy, such as Mental Health.
For more information , take a look at the following website – FACSNZ
Bring on November !!
We’ve got some Exciting Epilepsy things coming up in November. In a few days here in my home town, we have The Brain Train. The Brain Train is an event to really learn the facts, ins and outs of Epilepsy. We have some exciting speakers coming like my past Neurologist . People will really be able to have their questions answered by simply putting their hand in the air. People really do need to learn the facts. There isn’t enough public knowledge of Epilepsy. It’s also an opportunity for people with Epilepsy to realise that they are not alone.
So, next……Our Car Boot Sale !!
The New Zealand Epilepsy Foundation Support Group – Waikato .This is our group/board here in my home town. On the 8th of November we are having a Car Boot Sale. So, bring your Car or Ute along, pay a small fee and see if someone else is interested in a few things you no longer require. We’ll have the BBQ going, so it should be a productive morning. It’s exciting for us to get these events going. As we all know, actions speak louder than words.
I am also taking part in a November Epilepsy Blog Relay . Every day in November, someone will put forward a blog post around the subject of Epilepsy. There are a few subject within the subject of Epilepsy. My post will be about Genetics. Is someones Epilepsy Genetic ? Or are they the only one in their family with Epilepsy. I know for myself I’m the only one with Epilepsy. I’m also the only one in my family not wearing glasses. You never know what your gonna get.
It’s fantastic to be involved in all 3 of these activities. I love the feeling of being involved, working with others, making a contribution. Together everyone achieves more.
Yes, that’s right, no more Topiramate.
Tomorrow is my last day of Topiramate. I’ll then just be taking Levetiracetam and Lamotrigine. I have been in the process of cutting down to 2 drugs since my visit to the Neurologist in mid July. Each month I took 25 less. I was at 50 mg twice a day.
So, will this make a difference ? Who knows. I haven’t really been the best lately. At the end of last week, I had turns 4 days in a row. But it’s all emotional. What I mean by that is that most of the time I know why my turn happened, what brought it on. If we look at the year so far, I was better in the first half.
Here is my number of turns month by month.
- January – 3
- February – 3
- March – 4
- April – 4
- May – 6
- June – 6
- July – 4
- August – 6
- September – 4
- October ….so far – 5
So, has the small increase got anything to do with medication ? I don’t think so. We’ll have to wait and see. I’m still keen on seeing a Hypnotist. I did speak to one a while ago. He said they weren’t allowed to see the likes of myself, that they could be held accountable for anything that happens. There is a Hypnotist that advertising that she can relieve stress, confidence…. all types of emotional stuff. I’ll think I’ll give her a call sometime.
Let’s see if no Topriamate makes a difference. I’ve been on it for a very long time !!
Yes, it’s that time again !!
What time ? This week is the last week of the 3rd school term. So, here comes 2 weeks Holiday for our boy, and a week or so away from School for my wife ( she’s a teacher ) . Our girl normally just has one week off Kindy when the School Holidays are with us, but these holidays she’ll have both off.
So, as we do in alot of holidays, we’ll go to Gisborne and stay with my in-laws for a few nights. Might say with my parents at their beach house on the way home as well. Family is very important, and it’s fantastic for Grandparents and Great-Grandparents to spend time with the kids. My parents are lucky in that respect. They are only 15-20 minutes away and we see them at least once a week.
I always look forward to the school holidays because it means I’m not at home alone with the kids. I’m lucky in the respect that my wife is a teacher and she gets that week or so away. But please don’t say to me that teachers get alot of time off work though. They put in big hours during the school term and time at school is required during the holidays. It’s not a 9 am-3 pm job as many think it is.
My Epilepsy hasn’t been to bad lately, maybe slightly on the improve. So far this month I have had 3 turns. ( Complex Partial Seizures ) . Lets hope I can get to the end of the month without anymore. I’m currently in the process of ending taking Topiramate. They will be completely gone on the 20th of October. That will leave me on Lamotrigine & Levetiracetam.
Our daylight savings start this weekend . Bring on the summer. It’s slowly getting that tiny bit warmer. As I write it’s raining…. I’ll get wet when a go and get my daughter from Kindy in a wee while. Summer seems to get later and later every year.
Time certainly does fly. It seems like just yesterday it was last Christmas. Before you know it, it will be Christmas once again. There are good and bad parts to this. I do look forward to my daughter turning 5. ( Dec 2016 ) Alot of parents find this upsetting. Maybe I will when it actually happens. I have never been able to drive, so most of my days are at home, just the kids and I. A friend of ours, who’s son just turned 12 , said that it is frightening that his son is now 12. In a few more years, say 6, his son may be off on his own path. I fully understand where he is coming from. I also think of our parents getting older, like we all do. We can’t be here forever.
All the best,