We had a visit with our doc yesterday and nothing much came of it. Nicole was not very cooperative (surprise surpise) so Dr. T. couldn't even get close enough to see if the bandage contact was in place. We took her out and walked her for a LONG time to get her to fall asleep and went back to the clinic as per the doc. Of course by the time Dr. T. came to see her she was awake again...ugh. Long day for nothing.
On the bright side, Nicole hasn't required any painkillers today. We never did get a script for Gravol. The family doctor said no for under one year olds. He asked me what Nicole had done...corneal scraping I said...ohhhh that's painful. Yup. Nevertheless, she is doing much better today. Unfortunately, it seems her reflux is acting up and it's hard to tell if it's a sore throat from her breathing tube, all the screaming, or heartburn. I hope this clears in a couple of days. Mike and I both have callouses on our hands from swinging her in that carseat. It was the only thing that kept her quiet. Tomorrow morning we are going back to see Dr. T. and have the bandage contact removed. What the heck is a bandage contact anyways?? Apparently a large lens to cover the cornea. This should be fun.
Here's a pic of my poor pumpkin today...oh and Lilia enjoying Skittles...which of course she had to be reminded of not to share with Nicole =)
The story of a child with PHPV, a mom with MS, and our lucky little family.
Thursday, March 31, 2011
Tuesday, March 29, 2011
Disappointment
So, as most of you know and for those of you who don't, our little Nicole was booked for her goniotomy surgery yesterday. That's where they go in and try to open up blocked areas of the eye to help relieve some of the "backup" of fluid that causes glaucoma.
So....we were booked for noon. For any of you with babies you can only imagine having to withhold food for 6 hours. Usually we've been booked for first thing in the morning which doesn't seem as painful. Nevertheless, Nicole was a trooper. Of course the OR was behind which didn't help matters. We endured the whole horrible experience of putting our baby in hospital PJ's (although we've been through this enough that I brought booties from home for her this time), questionnaires, signing consents, handing her off to the OR nurse, and finally the dreaded wait in the surgical waiting room. We were lucky enough to have a visit from a wonderful friend...thanks Nicole! Then an hour and a half later out came Dr.T. Nicole did great with the anaesthesia and was waking up.....but....it was a no go for the surgery. Bubble burst. We were expecting complications but not a total no go. That never even crossed our minds. Apparently, her cornea was too hazy for Dr. T. to have a safe view of what she needed to do. They tried to scrape the cornea to clear it but it was unsuccessful. We now need to go the route of putting tubes in her eye. She explained the whole procedure, including the fact that there will be donor cornea keeping the tubes in place. I think that's when I stopped listening cause I was in total overload. We now wait to have the procedure organized since Dr. T. needs to have a retinal surgeon present in case of....so in a couple of weeks....back we go.
Now, we have the pleasure of caring for a 5 month old infant in horrible pain. I have never heard her shriek this way. We were told it was a painful procedure and to give Tylenol. Yeah, that didn't do a thing. By 8pm we were calling the resident on call. He said he was in the OR with Nicole and was half expecting this call. Well, if you were half expecting it why didn't you prepare us better??? I was ready to take her to ER for some morphine but he said the cornea heals in 24 hrs so we weren't likely to get a script for anything. In the meantime Tylenol/Advil and Gravol and it should be better by 24 hrs. Fine. That's what we are doing. She seems to have settled a bit but definitely does not want to eat. I put in a call to our family doctor to get some dosing for the Gravol. And that's where we're at. Poor thing looks like she's been beat up....but the sweetheart still smiles behind it all. Crazy how kids are such troopers.
Going in on Wednesday to have the "bandage contact" removed and see what's going on.
Will keep you all posted.
Thanks for all the love and support. It is all so very needed!
So....we were booked for noon. For any of you with babies you can only imagine having to withhold food for 6 hours. Usually we've been booked for first thing in the morning which doesn't seem as painful. Nevertheless, Nicole was a trooper. Of course the OR was behind which didn't help matters. We endured the whole horrible experience of putting our baby in hospital PJ's (although we've been through this enough that I brought booties from home for her this time), questionnaires, signing consents, handing her off to the OR nurse, and finally the dreaded wait in the surgical waiting room. We were lucky enough to have a visit from a wonderful friend...thanks Nicole! Then an hour and a half later out came Dr.T. Nicole did great with the anaesthesia and was waking up.....but....it was a no go for the surgery. Bubble burst. We were expecting complications but not a total no go. That never even crossed our minds. Apparently, her cornea was too hazy for Dr. T. to have a safe view of what she needed to do. They tried to scrape the cornea to clear it but it was unsuccessful. We now need to go the route of putting tubes in her eye. She explained the whole procedure, including the fact that there will be donor cornea keeping the tubes in place. I think that's when I stopped listening cause I was in total overload. We now wait to have the procedure organized since Dr. T. needs to have a retinal surgeon present in case of....so in a couple of weeks....back we go.
Now, we have the pleasure of caring for a 5 month old infant in horrible pain. I have never heard her shriek this way. We were told it was a painful procedure and to give Tylenol. Yeah, that didn't do a thing. By 8pm we were calling the resident on call. He said he was in the OR with Nicole and was half expecting this call. Well, if you were half expecting it why didn't you prepare us better??? I was ready to take her to ER for some morphine but he said the cornea heals in 24 hrs so we weren't likely to get a script for anything. In the meantime Tylenol/Advil and Gravol and it should be better by 24 hrs. Fine. That's what we are doing. She seems to have settled a bit but definitely does not want to eat. I put in a call to our family doctor to get some dosing for the Gravol. And that's where we're at. Poor thing looks like she's been beat up....but the sweetheart still smiles behind it all. Crazy how kids are such troopers.
Going in on Wednesday to have the "bandage contact" removed and see what's going on.
Will keep you all posted.
Thanks for all the love and support. It is all so very needed!
Friday, March 25, 2011
Project 365 - Week 12
| Mar 19 - Watchya doing in there? |
| Mar 20 - She was being a little too quiet playing with her dollhouse |
| Mar 21 - The apple doesn't fall far from the tree |
| Mar 22 - How did Lilia talk Baba into climbing in? |
| Mar 23 - Keeping occupied while Mommy does patch time |
| Mar 24 - Lilia thought we meant dump the diaperbag and climb in when we said let's try the new backpack carrier |
| Mar 25 - Monkey see monkey do....Lilia had to have her shades too! |
Wednesday, March 23, 2011
It's been awhile....
So, I have sat numerous times to update this blog with more than just Project 365 entries, but every time I just close the page and change my mind about what I want to say. Right now I am in a feel sorry for myself kinda place and no one likes a buzz kill so I've decided not to write about it. I'm feeling a lot of resentment towards this whole PHPV thing and I really don't want Nicole to ever come back and read this and think any of it was directed at her cause not one tiny ounce of it is. It's just that we are all tired and feeling a lot unlucky. Don't get me wrong. Nicole has been doing great. If I dare say it, patching is going OK. I can usually get almost 4 hours in without much fussing. It's just that the whole process is really tiring. When Nicole is patched she demands one on one attention. This is EXTREMELY difficult with a 2 year old running around. Lilia is so amazing and so patient and I am so very lucky to have her. If she'd had any ounce of "terrible twos" in her this whole thing would be unbearable. For the most part I can double duty it and play with Lilia while holding Nicole. Lilia is often right there with me shaking toys at Nicole. Sometimes it truly makes me laugh.....and then there was last week. Nicole had finished her patching and was getting a total kick out of Lilia running down the hall. Like full on belly laughs. Lilia loved it! It was the first time I'd seen the two truly interact. And then the next day Nicole was patched and poor Lilia had gotten it in her head that she was going to make her laugh again. She ran down that hallway full force and Nicole, of course did not laugh. The look of disappointment on my toddler's face was brutal. "She's not laughing" says Lilia. No sweetie she is not. I wish I knew the patching would be useful. But if she's not going to get any better vision than color and movement I don't want to do this anymore. But still everyday I lay that little baby down on her change table giggling away and slap that stupid patch on her and watch her smile fade away. I hate it. I hate every moment of it. But I do it for her. I do it cause I love her and want the best for her, even though it is by far the most difficult thing I have ever ever done in my life. Those moms reading this that are in the same boat get it....no one else can.
Now that's the honest truth. Like I said, in a feel sorry for myself kinda place....there's a lot more "woe is me" kinda stuff I could write but I don't actually want to be able to come back and read it. I am hoping that things will turn around soon, things will settle down and maybe one day I will forget all of this.
And now, on top of it all, I've realized I still have a needle waiting for me before bed. Lovely.
I am tempted to delete this post too....but I think maybe it's OK to feel this way sometimes. Makes the brighter days more special....
Here's to many sunny days soon!
Now that's the honest truth. Like I said, in a feel sorry for myself kinda place....there's a lot more "woe is me" kinda stuff I could write but I don't actually want to be able to come back and read it. I am hoping that things will turn around soon, things will settle down and maybe one day I will forget all of this.
And now, on top of it all, I've realized I still have a needle waiting for me before bed. Lovely.
I am tempted to delete this post too....but I think maybe it's OK to feel this way sometimes. Makes the brighter days more special....
Here's to many sunny days soon!
Saturday, March 19, 2011
Project 365 - Week 11
Hey...who can believe I'm still on track...woohoo!!
| Mar 12 - Not a good pic but had to remember this...Having fun with Dad |
| Mar 13 - Celebrating Baba's bday...Nicole was asleep on the floor |
| Mar 14 - It was 10:40pm and I had forgotten to take a picture....sizzling fire, oh no, sizzling chickens!! |
| Mar 15 - Hanging with our new buddies! |
| Mar 16 - I can't hear you! |
| Mar 16 - Let me see your foot... |
| Mar 17 - Fancy new plate |
| Mar 18 - Look who can roll over now! |
Saturday, March 12, 2011
Project 365 - Week 10
| Mar 5 - Styling new boots...thanks G! |
| Mar 6 - yum yum homemade donuts! |
| Mar 7 - Proud Daddy |
| Mar 8 - Professor Lilia |
| Mar 9 - Professor Nicole |
| Mar 10 - Getting into trouble |
| Mar 11 - Jump Jump Jump |
Thursday, March 10, 2011
Decision Made
Today Nicole had yet another visit to the Eye Clinic. We had a good chat with the doctor, I think we were in the room for an hour and a half total. Nicole, with much distractions, allowed Dr. T. to measure the pressure in her eye. Still high at 27-30 despite all the drops and medications. This means the glaucoma is still uncontrolled and that surgery is inevitable. Our goal now is not great vision (although we are still hopeful) but rather to give her a comfortable eye that does not look unsightly. Unfortunately, baby eyes are very pliable so high pressures stretch the eye. The high pressures can also eventually damage the optic nerve giving us no chance at vision at all. Dr. T. says we should be happy if Nicole can see color and movement. We are trying to give her a spare here in case something happens to her good eye...not get 20/20, but of course we are trying for the best. The plan now is for Dr.T. to talk to the retinal surgeon who did our initial operation and see if he is confident that the retina will not detach. If he gives it the OK Dr. T. will try to open up the area of the eye where fluid drains, and which is currently blocked. Wish I never had to know so much about the eye. Of course there are many complications, but right now the benefits outweigh the risks so we are going ahead with surgery. The other rough part is that post op we will have many exams under anaesthesia to see how the pressure is stabilizing. I cannot wait for Nicole to be big enough to sit still for pressure measurements, but for now she is 5 months old and having none of it. Can't bribe her with a lollipop just yet. =)
Unfortunately, my little one would not give me a chance to get her contact lens in (surprise surprise) so Dr. T. could not assess her vision. Given how crabby she is patched I don't suspect it is very good, but we are pushing through with the patching. Because Nicole is giving me such a hard time with the lens I have to wait for her morning nap to get it in. This results in half the day gone before we can patch....so....this brings us to her first pair of glasses!! Yes, we ordered a pair of glasses for her today. Hopefully we will be able to patch her for an hour before nap time and then I can slip that lens in. The glasses magnify everything so they are not optimal but right now they are better than nothing. I'll let you know how it goes once we get them!
Unfortunately, my little one would not give me a chance to get her contact lens in (surprise surprise) so Dr. T. could not assess her vision. Given how crabby she is patched I don't suspect it is very good, but we are pushing through with the patching. Because Nicole is giving me such a hard time with the lens I have to wait for her morning nap to get it in. This results in half the day gone before we can patch....so....this brings us to her first pair of glasses!! Yes, we ordered a pair of glasses for her today. Hopefully we will be able to patch her for an hour before nap time and then I can slip that lens in. The glasses magnify everything so they are not optimal but right now they are better than nothing. I'll let you know how it goes once we get them!
Monday, March 7, 2011
Project 365 - Week 9
| Feb 26 - Oops |
| Feb 26 - Best shirt ever |
| Feb 27 - Nicole's Baptism day |
| Feb 28 - Bedtime |
| Mar 1 - Yum, leftover cake |
| Mar 2 - Anyone feel like folding? |
| Mar 3 - Allo! |
| Mar 4 - Nicole's new buddy |
Wednesday, March 2, 2011
Project 365 - Week 8
A little late but still on track!
| Feb19 - What do you mean it's not for a toddler? |
| Feb 20 - For all those who don't believe I exist! |
| Feb 21 - Look I'm around again |
| Feb22 - Love my Jetta |
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| Feb 23 - Is someone having a party? |
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| Feb 24 - Hanging on in Recovery |
| Feb 25 - First time in the big bath! |
Monday, February 28, 2011
Happy Monday
One girl asleep, another one winding down with Daddy and a chance to sit down. The place is still a disaster after a very busy weekend but I'm too drained to care. We held Nicole's Baptism on Sunday and with that came lots of cooking and organizing and running around. On top of that we had Nicole's exam under anaesthesia (EUA) to worry about.
The EUA was on Thursday and little Nicole did very well. I am lucky that she doesn't usually wake up hungry so she doesn't complain when I don't feed her for these procedures. She had her last bottle at 3am and then sugar water with her meds at 5:30am. The EUA was at 930am. The procedure is to sign in 2 hours before then head up to get her changed into a hospital gown, weighed, checked, and give her eye drops. The eye drops are the worst part of the whole thing. She screamed and screamed and screamed....along with the little girl in the next room. The first drops are numbing drops which are suppose to take the sting out of the next 2 dilating drops. Don't think it works all that well. And the drops go into both eyes because while they are there they make sure her left eye is all good. (And it is.)
After all that fuss we are walked to the OR waiting room. There our ophthalmologist came to speak to us and have us sign consent to take her in. Then came the anaesthetist who had with him a medical student. The poor girl was so green you could spot her a mile away. The anaesthetist explained what he would be doing. He would put a mask on Nicole, put an IV in and then put in a breathing tube for the procedure. After I made sure he would be the one putting a breathing tube into my child and not the med student they were off. (Sorry, no practising on my little one.) Then the OR nurse came in and it was time for Nicole to go. Thankfully she was asleep. Still sucked.
The exam took over an hour. Felt like a zillion more. The doc finally came out and told us they took lots of measurements and photos. The pressure in her PHPV eye was down to 19 but still not enough so they added a 4th eye drop to our entourage. The long and short of it is that this will likely not correct itself so we need to decide whether we would like Nicole to have more surgery. What a horrible decision to have to make. It's definitely like being stuck between a rock and a hard spot. She stays on meds they may not be healthy for her. She has surgery she may have numerous complications resulting in more procedures and even possibly eye loss. We are trying to become more informed on all the options so when we go back to the Clinic in 2 weeks we can have an educated conversation and be confident with our decision.
We have also been upped on patch time. It's now gone from 2 hours to 4. We have only been able to get up to about 3.5 hours before Nicole just loses it. I still think that's pretty good. We also have a new contact thanks to the change in eye shape from the glaucoma.
And I think that's about it for now. Just trying to get through it all....one day at a time....
The EUA was on Thursday and little Nicole did very well. I am lucky that she doesn't usually wake up hungry so she doesn't complain when I don't feed her for these procedures. She had her last bottle at 3am and then sugar water with her meds at 5:30am. The EUA was at 930am. The procedure is to sign in 2 hours before then head up to get her changed into a hospital gown, weighed, checked, and give her eye drops. The eye drops are the worst part of the whole thing. She screamed and screamed and screamed....along with the little girl in the next room. The first drops are numbing drops which are suppose to take the sting out of the next 2 dilating drops. Don't think it works all that well. And the drops go into both eyes because while they are there they make sure her left eye is all good. (And it is.)
After all that fuss we are walked to the OR waiting room. There our ophthalmologist came to speak to us and have us sign consent to take her in. Then came the anaesthetist who had with him a medical student. The poor girl was so green you could spot her a mile away. The anaesthetist explained what he would be doing. He would put a mask on Nicole, put an IV in and then put in a breathing tube for the procedure. After I made sure he would be the one putting a breathing tube into my child and not the med student they were off. (Sorry, no practising on my little one.) Then the OR nurse came in and it was time for Nicole to go. Thankfully she was asleep. Still sucked.
The exam took over an hour. Felt like a zillion more. The doc finally came out and told us they took lots of measurements and photos. The pressure in her PHPV eye was down to 19 but still not enough so they added a 4th eye drop to our entourage. The long and short of it is that this will likely not correct itself so we need to decide whether we would like Nicole to have more surgery. What a horrible decision to have to make. It's definitely like being stuck between a rock and a hard spot. She stays on meds they may not be healthy for her. She has surgery she may have numerous complications resulting in more procedures and even possibly eye loss. We are trying to become more informed on all the options so when we go back to the Clinic in 2 weeks we can have an educated conversation and be confident with our decision.
We have also been upped on patch time. It's now gone from 2 hours to 4. We have only been able to get up to about 3.5 hours before Nicole just loses it. I still think that's pretty good. We also have a new contact thanks to the change in eye shape from the glaucoma.
And I think that's about it for now. Just trying to get through it all....one day at a time....
Thursday, February 24, 2011
We're Home!
Just a quick note to let everyone know Nicole did great during her examination under anaesthesia (EUA) today. She was sleepy earlier today but was back to her smiling, laughing self tonight. We are up to 4 different types of eyedrops on top of the 4 times daily oral med so we are feeling a little tired. I will definitely fill in all the details as soon as I can sit down properly.
Thanks everyone for all your support...it means so very much to us!
Thanks everyone for all your support...it means so very much to us!
Saturday, February 19, 2011
Project 365 - Week 7
| Feb 12 - Lilia's addition to Mike's lunch |
| Feb 13 - Zoom zoom zoom we're going to the moon! |
| Feb 14 - Aren't we 3 lucky girls? |
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| Feb 15 - A note to Nicole...isn't she lucky? |
| Feb 15 - Be polite and send a note back! |
| Feb 16 - Who needs a chair? |
| Feb 17 - Taking out a contact during Nicole's ER visit |
| Feb 18 - Just looking through her PJ drawer |
Friday, February 18, 2011
Too Much Excitement
So quick post to update on our latest fiasco. So Nicole started her oral meds on Tuesday for glaucoma. It coincided with the worsening of a wicked cold she got from her sister. Two days later she refused to eat....like at all. I think she had a total of one bottle all day. She had a horrible cough, terrible runny nose and her breathing was really really quick. Enough to send her RT mom and paramedic dad over the top =)
Anyhow, it was 4:00pm yesterday and I thought I would call the Eye Clinic to see if anyone was still around to tell me if there was any issue with continuing the oral meds when she hasn't been eating. The response I got was, stop the meds and take her straight to the ER here. I was likely lovely. They were afraid that Nicole had gotten dehydrated. (The oral med is actually a diuretic) So downtown we went in rush hour. To make a long story short we were in and out in 3 hours with the answer of...no she is not dehydrated and she is not eating cause she has a virus, nothing to do with the oral meds. So now I feel like THAT mom. They sent us home and told us to get the Hydra sense nasal aspirator (yum) and clean her out before feeds. And I could restart her oral meds. By the way, the aspirator, albeit very gross, works AMAZING! Nicole is back to almost normal feeding!
So that was our ER story. The funniest part is that the Resident who saw us was actually in Ophthalmology. All he wanted to do was look in her eye. (Nicole was kind enough to let him). He thought it was the coolest thing. You know he went home and called all his Ophthalmology buddies and told them all about what he got to see. I'm sure he's only read about this in a textbook. LOL. We thought it was hilarious that Nicole was there to be assessed for eating issues and he just kept looking in her eye. Then he was like, see you next year at the Clinic!! Too funny.
So that was our excitement yesterday. Thankfully, all is back to normal. Well normal for us anyways. =)
Anyhow, it was 4:00pm yesterday and I thought I would call the Eye Clinic to see if anyone was still around to tell me if there was any issue with continuing the oral meds when she hasn't been eating. The response I got was, stop the meds and take her straight to the ER here. I was likely lovely. They were afraid that Nicole had gotten dehydrated. (The oral med is actually a diuretic) So downtown we went in rush hour. To make a long story short we were in and out in 3 hours with the answer of...no she is not dehydrated and she is not eating cause she has a virus, nothing to do with the oral meds. So now I feel like THAT mom. They sent us home and told us to get the Hydra sense nasal aspirator (yum) and clean her out before feeds. And I could restart her oral meds. By the way, the aspirator, albeit very gross, works AMAZING! Nicole is back to almost normal feeding!
So that was our ER story. The funniest part is that the Resident who saw us was actually in Ophthalmology. All he wanted to do was look in her eye. (Nicole was kind enough to let him). He thought it was the coolest thing. You know he went home and called all his Ophthalmology buddies and told them all about what he got to see. I'm sure he's only read about this in a textbook. LOL. We thought it was hilarious that Nicole was there to be assessed for eating issues and he just kept looking in her eye. Then he was like, see you next year at the Clinic!! Too funny.
So that was our excitement yesterday. Thankfully, all is back to normal. Well normal for us anyways. =)
Tuesday, February 15, 2011
Nicole's Followup
So last night I had to stop feeding Nicole at 2:30am for the potential sedation this morning. I couldn't figure out the best way to max out what she could eat. I decided to "dream feed" her at 11:00pm and then wake up at 2:30am to give her another bottle. It kinda backfired...she wasn't all that hungry at 2:30am and didn't really eat much. Then when we got her up early this morning to go downtown she was really crabby. While I was putting in her eye drops I could hear her stomach growl. Poor soul. I knew it would be a long day but refused to eat until my baby could. We left home early, never know what kind of traffic to anticipate. Needless to say we got to the hospital really early and had to kill more than an hour. Nicole refused to sleep. Can you blame her? She was starving! And then just as we started to head to the clinic to register she passed out. Woohoo. And guess what??? She STAYED ASLEEP!! She stayed asleep for Dr. T. to examine her so we avoided the dreaded sedation!! How awesome is that!?
OK, so here's the scoop. The drops have worked a little. Her cornea is slightly less cloudy but the numbers are still quite high. The way Dr. T. explained it to us was that each machine reads the pressure differently, and it will read differently depending on what the child is doing at the time. She says the best way to look at it is to compare the value difference with the good eye. Last week the intraocular pressure (IOP) was reading anywhere from 27-50 in Nicole's PHPV eye. Her good eye was 8. Today the good eye was 16 and her other eye was 34. So we received a prescription for oral medication (Diamox...can you believe it??). She hates it. She has to take it four times a day and I basically have to continuously scoop it back into her mouth. Fun. We are booked for....big breath....our first examination under anaesthesia next week. Sigh. I knew it was coming. This basically means she goes to the OR and gets put to sleep so the doc can have a good look in her eye. Dr. T thinks it's the best way for Nicole right now. I am not sure how I feel about it yet. I know I'm scared. I hate handing her off to a stranger. But I know she's safe and in good hands there too. I guess it's just a necessary evil.
I am finding the morning and evening rituals of drops, meds (don't forget the reflux meds too....will be glad when she outgrows that!) and contact lens insertion/removal exhausting. Especially having a toddler running around too. So now that the two girls are asleep I am going to ignore all the toys and crafts scattered everywhere, climb right over them to sit and watch some TV with my hubby and try for a moment to forget about all this. At least until morning.
OK, so here's the scoop. The drops have worked a little. Her cornea is slightly less cloudy but the numbers are still quite high. The way Dr. T. explained it to us was that each machine reads the pressure differently, and it will read differently depending on what the child is doing at the time. She says the best way to look at it is to compare the value difference with the good eye. Last week the intraocular pressure (IOP) was reading anywhere from 27-50 in Nicole's PHPV eye. Her good eye was 8. Today the good eye was 16 and her other eye was 34. So we received a prescription for oral medication (Diamox...can you believe it??). She hates it. She has to take it four times a day and I basically have to continuously scoop it back into her mouth. Fun. We are booked for....big breath....our first examination under anaesthesia next week. Sigh. I knew it was coming. This basically means she goes to the OR and gets put to sleep so the doc can have a good look in her eye. Dr. T thinks it's the best way for Nicole right now. I am not sure how I feel about it yet. I know I'm scared. I hate handing her off to a stranger. But I know she's safe and in good hands there too. I guess it's just a necessary evil.
I am finding the morning and evening rituals of drops, meds (don't forget the reflux meds too....will be glad when she outgrows that!) and contact lens insertion/removal exhausting. Especially having a toddler running around too. So now that the two girls are asleep I am going to ignore all the toys and crafts scattered everywhere, climb right over them to sit and watch some TV with my hubby and try for a moment to forget about all this. At least until morning.
Monday, February 14, 2011
Fellow Moms
Tomorrow is the big day. Nicole is getting sedated again for a checkup. I wish they'd slip a little something to me too...would make it a heck of a lot easier =)
One thing that does make it easier is having some great support from fellow moms. The internet is a wonderful thing. I've joined a couple of yahoo groups for PHPV and Aphakic kids. It's a place to go and just ask questions from other moms (and dads =) ) who are going through the same thing or been there before. Without these groups I'd never have made it through the past 4 months. I've been lucky to have found some great moms to share the journey with.
Thanks B. for sharing your stories, support, and pictures. When we've come out strong at the other end like you have I will definitely pay it forward.
J.U.H - Thanks for giving us some laughs about how to respond to the inevitable "why" questions from strangers. Really, why else would someone be wearing glasses!!??
J.W. - You are awesome. Look forward to travelling this road with you. Loved loved loved the picture. Maybe I can talk you into letting me share it here =)
And to all the other moms and dads who've taken the time to answer my questions....it is all so very appreciated.
Now it's off to sleep....alarm set to fit a feed in before cut off time!
Wish us luck!
One thing that does make it easier is having some great support from fellow moms. The internet is a wonderful thing. I've joined a couple of yahoo groups for PHPV and Aphakic kids. It's a place to go and just ask questions from other moms (and dads =) ) who are going through the same thing or been there before. Without these groups I'd never have made it through the past 4 months. I've been lucky to have found some great moms to share the journey with.
Thanks B. for sharing your stories, support, and pictures. When we've come out strong at the other end like you have I will definitely pay it forward.
J.U.H - Thanks for giving us some laughs about how to respond to the inevitable "why" questions from strangers. Really, why else would someone be wearing glasses!!??
J.W. - You are awesome. Look forward to travelling this road with you. Loved loved loved the picture. Maybe I can talk you into letting me share it here =)
And to all the other moms and dads who've taken the time to answer my questions....it is all so very appreciated.
Now it's off to sleep....alarm set to fit a feed in before cut off time!
Wish us luck!
Sunday, February 13, 2011
Project 365 - Week 6
| Feb 5 - What? You don't want me to take your picture? |
| Feb 6 - Cereal time! For some reason I can't turn this picture! |
| Feb 7 - Taking a walk with the snowblower |
| Feb 8 - My smiling beauty |
| Feb 9 - Decorating a cake |
| Feb 10 - Here we go again |
| Feb 11 - Happy Birthday A.! |
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