Friday, 5 January 2018
Hidden emotions ~My journey through grief
Labels:
antenatal anomaly screening,
bereavement,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
life after loosing my baby,
pregnancy or infant loss,
The journey of a grieving mother
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Sunday, 31 December 2017
New year, New chapter 2018
Another year nearly down and ready for the next chapter in our lives, ready for the new year to make more amazing memories with my close friends and family and ready to learn more life lessons. Never a day goes by without remembering those precious moments with my amazing daughter who is always in my heart, still feels like it was only yesterday she was in my arms, and my dear grandad who I miss dearly. I've learned soo much this past year and embrace each day I have with my loved ones, feel incredibly lucky to have Kevin always by my side and Keelan who always wakes up with a smile on his face, I feel blessed to have my mum and nan and all our family and friends who support us in each and every way. Blessing all our angels in heaven and blessing you all for health, friendship, and love for 2018 and for ever more. Xxx
Labels:
chd awareness,
life after loosing my baby,
mother to an angel,
pregnancy or infant loss,
The journey of a grieving mother
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Monday, 22 May 2017
Happy 1st Birthday to our Angel Isabella
It's hard to believe it's one year today, all I keep thinking about is this time last year she was with us, I keep getting flash backs of the joy she brought us when she was born, and then the heartbreak and pain in which we could not save her.
I somehow found comfort in the fact that she was with us this time last year, and I am petrified of the thought now that i can no longer say this as crazy as it may sound.
We should be getting ready for her first birthday party, but instead I am trying to find something that is weather proof to place on her grave, something I never thought I would be doing.
In my head I want everything perfect and why not, I am still a mother who wants the best for her children. The process in which all parents have to go through, the first of anything is the hardest but keeping in mind that she is watching over us all and growing on the other side some how brings me to a smile.
Would you believe I saw a red butterfly today, it made me think of her, but this time it was not white as I would always see, it was a bright red, I like to think that's a sign from her telling me she is growing, and that she is around us always.
Happy 1st birthday our darling Isabella, from mum, dad and your big brother Keelan xx
Labels:
Hypoplastic left heart syndrome,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
NILMDTS,
pregnancy or infant loss,
The journey of a grieving mother
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Monday, 15 May 2017
Universal access to Foetal Anomaly screening to be made for Women Nationwide
Myself and
Kevin are delighted to announce the passing of a Dail Motion by Sinn Fein’s
Health Spokesperson T.D Louise O’Reilly who highlighted the current issues
within Irelands Maternity Services. The motion included universal access to
foetal anomaly screening across all Maternity Hospitals Nationwide, the full
implementation of the National Maternity Strategy and a commitment to work with
nursing and medical unions in the recruitment and retention of medical staff so
that all maternity hospitals meet the ‘Birth rate plus standard’ for midwifery
staffing, as well as international standards for consultant obstetricians and
gynecologists.
Louise O’Reilly
has called on the Minister for Health to swiftly implement the commitments made
in the Dail with regards to the National Maternity Hospitals, she said that it
is now up to the Government to stand by their commitment and that she will be
following up with the Minister to ensure implementation of these incentives.
This is a major victory for Women’s Health and the Minister must now accept the
collective will of the Dail and act on the motion.
Words will
never be able to describe our emotions, we are still travelling through our
journey of loss, but we will always truly believe our angel was sent to us for
a reason and this news just proved that.
Since the
day I received a message from Cllr Damien Quigg who showed so much compassion
for our campaign and pure dedication we believed as a small group of people we
can make change. Cllr Damien Quigg connected us with T.D Louise O’Reilly during
our Dublin visit for my Ireland AM interview, and I will always remember
sitting in the room with my good friend Shauna, a fellow heart mum while we
both told her our stories, I knew instantly from her reaction that she would
not rest until our voices were heard and that is exactly what she did.
All those
parents who spoke out about their heartbreaking experiences, the media who took
it in their stride to share our journeys, to Cllr Damien Quigg who supported
our campaign and set us in a direction were we would not have been able to go
without him, and to T.D Louise O’Reilly who made not only our voices heard but
the voices of all our angels in a place where change can be made, once implemented
babies lives will be saved as a diagnosis will be made prior to birth, and
parents to be, will be getting the service they deserve.
Its been
such an incredibly hard time for us this last year and our Isabella’s birthday
and anniversary is only around the corner but I truly hope with all my heart that
she knows she helped make this change.
In memory of our Isabella, our very own angel.
Labels:
20 week anomaly scan,
chdawareness,
child health,
Cllr. Damian Quigg,
foetal anomaly screening Ireland,
maternity services,
Minister of Health Simon Harris,
national maternity strategy,
TD Louise O'Reily
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Monday, 20 February 2017
Meeting with National Programme Director for Women and Infants’ Health
Well since we started our Isabella’s campaign to raise awareness of CHD
and promote that all women in Ireland should be entitled to the 20 week
screening, we’ve received continual support from many families who have
travelled a similar path as myself and Kevin, I feel through our own pain like
many others are going through, it helps to speak to those who know and feel the
same heartbreak.
Reading peoples stories, some with happy endings and others with sad, it
really has given me even more drive to push this as much as we can. I still
remember writing all our memories of Isabella to try and keep her alive in us,
and even though she was only here on earth for a short time she incredibly left
her mark.
With the help of the media making our voices heard the HSE are now listening.
Since we gained a response from the Minister for Health Simon Harris I received
an email from Kilian McGrane, who is the newly appointed ‘National Programme
Director for Women and Infants’ Health and will be rolling out the programme to
introduce the 20 week anomaly scan to all expectant mothers nationwide . Minister
Simon Harris forwarded my email to Mr McGrane and asked for him to meet with me
regarding our campaign for anomaly scanning.
In recent weeks Mr McGrane has contacted me and welcomed an opportunity
to meet with me to discuss the important issues raised in my email to the
Minister.
I will be meeting with Mr McGrane at Tralee University Hospital on
Wednesday 22nd February, he will also be joined with the recently appointed
clinician, Dr Peter McKenna, who is the Clinical Lead for the Programme.
In the meeting I will be giving an insight from a parents perspective
from our own personal journey and what we feel needs to be addressed, from the
much needed scan to also highlighting
the lack of after care service to families whose baby passes away, specifically
for parents and the siblings.
If you have had a similar experience or know someone
who has and would like to raise any questions please feel free to contact me prior
to my meeting and I will ensure your voice is heard.
I will keep you all updated, and I know Isabella
will be with me.
Email: jazminesands@gmail.com
Mother to an angel
Labels:
20 week anomaly screening. expectant mothers,
bereavement,
chd awareness,
HSE,
Hypoplastic left heart syndrome,
Ireland,
The journey of a grieving mother
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Thursday, 19 January 2017
Equal access to standardized ultrasound services to be implemented throughout all maternity units
I am
delighted to announce that since our campaign started for the right of all
expectant mothers to be given routine detailed screening, we are finally seeing
progress made. Minister for Health Simon Harris emailed me today confirming
that the HSE National Service Plan 2016 committed to the planning and development
of equitable access to antenatal anomaly screening throughout all maternity
units in the context of emerging maternity networks.
In addition,
the National Maternity Strategy is now clear that all women must and will have
equal access to standardized ultrasound services. This strategy will be implemented
on a phased basis over the coming years which will be led by the National Women
& Infants Health Programme.
The newly
appointed Director will be meeting with me in due course to discuss the
strategy going forward, in this meeting I will be also highlighting the after
care service for families who suffer loss of their baby, which through our own experience
is seriously neglected.
Words cannot
describe how we are feeling now, from such a dark and sad time in our lives our
beautiful daughter shed some light from heaven, I knew in my heart she was sent
here for a reason, I am so proud of our angel. Our campaign was never darkened
around negativity, through our experience we saw a fault in the health care of
maternity services and in our daughters memory we simply did not want anyone
else to go through what we and many other families have gone through. I have
always said that we wanted to work alongside the HSE and not against it and now
they have started to implement a plan for all expectant mothers to receive
routine anomaly screening nationwide so if anything has been detected proper
procedures can be put in place before birth giving all babies a fighting
chance.
I am blown
away from all the support we have received since Isabella was born and when she
grew her wings, I am so proud to be her mum, she is around us always and
throughout our campaign this miracle has just proved it.
I will keep
you all updated on further progress as this is only the beginning.
Mother to an angel
xoxox
Labels:
antenatal anomaly screening,
chdawareness,
Crumlin,
HSE,
Ireland,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
life after loosing my baby,
Minister for Health Simon Harris,
NILMDTS
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Tuesday, 13 December 2016
The months after is when you need support the most
I know it has been a while since my
last post, but I don’t want to just write every week, this is a real life
journey and I only write when I feel it is the right time to share my recent experiences I’ve had while living
life after great loss.
Everyday life since losing Isabella
has changed, small things you don’t notice during your daily routines all of a
sudden becomes a big deal, at one point I felt every time I left the house all
I would see is babies and baby stuff everywhere; my anxiety grew so much I just
wanted to stay at home all the time, my house became my sanctuary for me, my
haven, my own space to lock myself away from society, I would always say to
myself, ‘how and when will I start to cope’.
(In recent months i’ve found grief is truly like the ocean, it
comes in waves and sometimes can consume you when you least expect it, don’t fight
your emotions, roll with them like those waves, the more you fight and hold
back the worse you will feel to which point you may sink into the deep dark
obis of depression.)
I wake up every
day to my routines of life itself, then all of a sudden it just hits me that I
lost my daughter and will never be able to hold her in my arms again, it really
does consume me at different times of the day but I am still learning to remind
myself of the fact we had the chance to look into her beautiful eyes, while she
stared right back at us knowing that she was loved unconditionally, these
thoughts are what keeps me looking forward.
The support we had after Isabella was born and when she grew her wings was just amazing, our close friends and family helped organise her burial and really showed so much love and light during a time of such darkness. The following weeks we had people calling to our house on a daily basis which kept us going but looking back now I can see that it hadn’t sunk in still, we were numb, in shock, I knew what had happened but I hadn’t processed the fact that we have lost our baby girl. I do think that if it wasn’t for Keelan I could have sunk much lower, but this is a point you feel you’re at a cross roads and must try your best to continue on and learn to live your life after such a loss. I remember so clearly waking up the following morning after our final goodbye, the sun was shining so bright through our curtains, we just laid there in silence, in a state of shock not knowing what to do with ourselves, the door bell rang constantly by people calling to us, and at the time I just wanted to be left alone, but I got up as I did not want to look weak and then dived into washing all our clothes from Dublin, I washed the same clothes 2 or 3 times just to keep myself busy, as crazy as it sounds thinking about it now I just wanted to feel human again, I was trying to imagine that I would be doing this if she was still there and asleep in her mosses basket, I just wanted to feel like a mother to a new born baby while trying to block out the pain in case I fell apart even though inside I was broken, empty and felt useless.
I have come to the realization that
support is needed more than ever months after losing a loved one, most people
would presume as months have passed you start to learn how to cope, as they say ‘time
is a great healer’ which it is very true however, emotions would start to
sink in during the later stages of grief, when your days quieter down and people
stop calling as much, this is when you have more time to think to yourself
about what has happened, this is the crucial time you will need support.
I am so thankful for my group of
close friends who have been travelling this journey alongside me, who knows
when I am having a bad day or week, who would call for a cup of tea to talk
about everything and listen to me, or just sit there in silence with me just so
I feel their company there with me, letting me know I am not alone. I feel it is very important to share this if
you know someone who is currently grieving that support is very much needed when
months have passed, whether it’s a call, a text or just passing through for tea
anything just to show that someone is still thinking of you would mean the absolute
world, I know this because it means everything to me and has helped me get
through the dark days.
If you are the one going through the
pain of loss you must keep talking and if you need someone to listen to you,
you must pick up your phone or call to your friends or families house because
talking is key to a healthy mind, remember it’s not getting over something like
this it is learning to cope with it, this is what I have learned so far and still have so much to come.
Thank you to my friends and family
xoxox
Labels:
angel mum,
bereavement,
chdawareness,
congenital heart,
Crumlin,
HPLHS,
life after loosing my baby,
months after loosing a baby,
neonatal,
neonataldeath,
The journey of a grieving mother
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Saturday, 12 November 2016
Isabella's CHD Awareness & Pregnancy Screening Campaign Video ~ Please share
I created this video to help promote our campaign for all women in Ireland to be entitled to a
' free routine 20 week scan'.
' free routine 20 week scan'.
When our beautiful baby Isabella was born we were told everything was fine until a few hours passed and she had to be rushed to Dublin finding out that she had Hypo-plastic Left Heart Syndrome along with many other complications with her heart, they could not offer her surgery and so she grew her wings 5 days later.
Isabella's fate could not have been changed however if it could have been different and she could have had surgery she could of well passed away upon birth as her heart condition was not picked up as this simple scan is not offered to all expectant women in Ireland.
We do not want any other parent to go through the journey we have and are still going through.
We are waiting for Minister of Health Simon Harris to listen to our story and hopefully together make some change for our future babies of Ireland.
Please share, thank you
Mother to an angel xx
Labels:
chdawareness,
Hypoplastic left heart syndrome,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
Minister of Health Simon Harris,
pregnancy,
scans,
The journey of a grieving mother
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Is it just coincidence or is our angel talking to us?
I am a big believer
in life after death, I have been since I was a little girl through my own personal
experiences, I think when someone close to you passes away you just have hope to
have some kind of sign from them to let you know they are ok, but at the same
time you do not want to drive yourself mad looking for it and be disappointed if
you don’t see or hear from your loved one.
I am open
about what I believe in and accept everyone has their own opinions about this
topic but I wanted to write about this as I feel many people who has suffered
loss always wonders if their loved ones are around them and some may even crave
for some kind of sign which is exactly how I feel.
Only last
week myself and Kevin were in our local Smyths store starting our Christmas
shopping, we don’t get to do too many things with just ourselves as we are
always busy so it was nice to have some quality time with just the two of us,
as we waited in the queue with our hands full of prezzies I noticed this little
girl skipping past me with long dark hair she was stunning, my heart melted and
just smiled to myself trying to keep it together in front of Kevin and of
course everyone else around me, it was when I heard her mother call her name ‘Isabella’....
I literally lost my breath from the pure shock of hearing her name, I looked directly
at Kevin and his face just turn pure white, I wanted to drop everything and
run, I could not believe it out of all the names we hear hers, I have never
heard her name before as it is unusual which is why we choose it, why did we
hear it, how was it that out of all of the places in the shop she said her name
right in front of us, we walked out and tears were just pouring down my face
feeling the pain of emptiness and realizing that we should be shopping for our
2 children and not one.
As we drove back I thought to myself, what if
this was meant to happen but to not upset us but as a message to let us know
she is around us always, I suppose it is turning a negative situation into a
positive and seeing things in a different light instead of darkness.
During
Isabella’s burial I asked one of my good friends to arrange a white dove to be
released, I thought this could be a symbolic sign for her spirit to be released
to the heavens above, my heart melted when she walked up towards us with a
beautiful white basket, she opened it up and there the dove looked at us and
then flew up into the sky, I looked up and noticed the sun breaking through the
fluffy clouds as if an opening appeared welcoming our baby girl.
A few days past when Kevin’s brother said that he went to visit her grave and noticed a
white butterfly on her cross, as soon as I heard I liked to think it was her
letting him know she was still around, that very same week Kevin was in the
garden and felt something on his hand, to his amazement it was a white
butterfly, as he told me I could see in his face full of hope that it was a
sign but I couldn’t help feel the emotion of jealously, why not me? Why as her
mother have I not had a sign, I felt maybe I did do something wrong that I didn’t
deserve it, but not long after she did said hello or so I like to believe.
I remember
it was the day of Bike Fest in Killarney, one of Kevins good friends arranged
for him to have a tattoo to honor our Isabella which meant the world to Kevin,
I remember I was sitting in the garden looking up in the sky waiting to leave,
I looked across the garden and there the white butterfly flew across and over
the fence, there it was my little sign, a tear ran down my cheek knowing in my
heart she was letting me know she was around, that very same day my Nan called
to check up on me I remember her words as clear as day, she said ‘ I am sitting here in the sun in my garden
and I saw a beautiful white butterfly just came out of nowhere and flew right
in front of me and it reminded me of our Isabella’ the phone went quite as I tried to process
what my Nan just said to me, did I tell her? No I didn’t, out of anything that
could have happened as a sign it was linked to a white butterfly, I then
explained to her what has been happening and she said that it sounded like she
wanted us to know she is always around.
I know this
may sound out there, but isn’t it lovely to think something like this is symbolic,
what is the harm in thinking this way? There is no harm in thinking or
presuming this being linked but you would have to question is this just a
coincidence? or is our little angel talking to us in her own little way,
letting us know that she is still around us....well, I like to think it’s her,
if you have a loved one and notice a sign, do not just ignore it and think you
are just over thinking it, you should embrace it, believe it is a message from
above saying hello, they are ok and they will always be around you..
Mother to an angel xx
Labels:
angel,
baby,
bereavement,
chd awareness,
grieving siblings,
Is it just coincidence or is our angel talking to us?,
mother to an angel,
NILMDTS,
pregnancy or infant loss
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Wednesday, 26 October 2016
The journey of a grieving mother
‘I am sorry but there
is nothing we can do to save your daughter’ these are the words that constantly
replay around in my head, visions of me holding her with her big beautiful eyes,
remembering every single expression she done while here on earth, from the
small lines on her forehead as she looked up at me, to her perfectly shaped
little mouth that I used to stroke ever so gently. No one can comprehend the
loss of your own child unless they have walked the same path, from witnessing
her last breath and yet feeling totally helpless as a parent to save her,
something that was my duty, a duty to protect a duty that goes beyond anything
else, a duty I feel as a mother failed to do.
Since we found out we
were expecting, I made sure that everything I was eating and drinking would
benefit our baby, I didn’t smoke or drink, I ate more veg, fruit, salad and
drank as much water as I could, I stayed at home most of the time but I was
happy, happy to ensure that our baby was safe and everything was going to be
perfect.
The day we travelled back
to Kerry was the same day we laid our daughter to rest, that very same evening
we walked into our house, I remember it was quiet, I walked upstairs and there in
front of me was the door for her nursery, untouched, everything in place ready
for her, I grabbed my stomach and all of a sudden I felt ‘emptiness’, despair, sadness,
failure of a mother, I walked into her room, everything was perfectly placed,
her cot, changing station, nappies and baby wipes stocked up, even a towel
ready by the side for her first wash, I looked down at my hands and nothing was
there only drops of my tears. I sat on the floor and cried so hard it hurt,
clenching on her blanket so tight, I held it as if she was there, just trying
to see if I could feel like how it should be, am I going mad? No, I just could
not register that she was gone and I was to never see her again in this life. I remember the curtains in her room were open,
the stars were so bright that night, I walked to the window and felt a wave of calm
that she was there with me watching me through the stars.
During her burial I
felt I could not let my true emotion out, if I started to cry I was petrified
that I would not stop, I would collapse and not get back up, I have this
constant feeling that my body had failed my daughter, that it was my fault she
is not here today, the least I could of done was be strong for her before she
flew with the angles, just like she was strong for us by giving us time.
It has already been 5
months since we welcomed her here and my heart is still so raw, I feel so much
fear as time goes on, as my memories of her become slightly more faded, the
emptiness has grown even more while I am here at home, I should have lack of sleep,
I should be making bottles and have washing so high I don’t know where to
start, but as soon as Keelan has gone to school I am left in the house of
silence ... I look around and feel deflated, I try and keep myself busy making
sure the house is perfect, washing is done but I find myself looking at the
time counting down the hours Keelan will be home, to see his smile again, tell
me about his day work together on his homework, then its time to make the
dinner, Kevin comes home talks about his day I clean up after dinner, chill out
then bedtime and repeat all the above. Being at home alday is a constant
reminder of someone precious that I do not have, go for a walk I say, it will
do me some good, so I do I start to feel positive again, I am walking taking in
the fresh air, I then look ahead and see a lady with a pram, my heart races every
time, it’s not their fault but in my mind it brings back the constant reminder
of my most biggest loss.
The eagerness of
wanting some normality is taking over, I want to get back into work I am ready
and so the job search continues sending CV’s and not hearing back makes me feel
even more worthless, the recent loss of my granddad who was such a large factor
in my life overwhelms me, is my life ever going to give me a break? I know
there is always someone else more worse off but this is my feelings, my
emotions and my battle as an angel mum which I think many other angel mums
could relate too. I envy those people who have their career, see and talk to
different people every single day, I am doing everything I can to get back in
to some normality but I have to keep reminding myself that things do take time,
grief is a process and I am only at the beginning. I have Keelan to think about my son who is my world, so I must try and pick myself up again and so I am starting tonight by going for a long walk, I now want to focus on getting myself fit agian mind and body, i've got to do this, I will do this and any bumps along the way I will jump over them with pure determination.
This is only the beginning of my journey....
This is only the beginning of my journey....
Mother to an angel xox
Labels:
bereavement,
chd awareness,
life after loosing my baby,
october pregnancy and infant loss awareness month,
pregnancy or infant loss,
The journey of a grieving mother
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Friday, 21 October 2016
Campaign Update - Letter to Minister for Health
Email sent to Minister for Health Simon Harris regarding our meet request
Sent 5/10/2016
Dear Minister,
Further to the full support from the ‘Southern Regional Health Forum’ I would like to ask for an opportunity to meet with you and discuss our campaign which highlights just how crucial it would be to have routine detailed screening available to all expectant mothers.
With a routine detailed 20 week scan put in place this will relieve much strain for Crumlin as plans can be put in place prior to the birth. Currently babies who need immediate medical attention must wait for the arrival of an ambulance then they must be transported to Dublin which can take a considerable amount of time, which in most cases they simply do not have.
If a routine detailed 20 week scan was implemented and a diagnosis was made prior to the birth, a surgical plan can be made and the mother would have the opportunity to make arrangements to deliver her baby in Dublin which would also increase the survival rate of the baby. We understand that our daughter could not have been saved, however we are speaking from our own personal experience as we wish no other parent to have to go through what we have gone through, we are also speaking on behalf of the hundreds of parents who have contacted us and bravely shared their stories of babies who did pass away because a diagnosis was not made.
Minister we ask if you could meet with us at your earliest convenience to discuss our campaign further, we hope through our letter to you, you can understand the urgency to address the current screening procedures and hopefully going forward we could have an opportunity to work alongside the HSE.
Thank you for your time, and we look forward to receiving your response.
Kindest regards
Jazmine Sands
Labels:
baby,
chd awareness,
Dail,
Dublin,
Glow hearts for Crumlin,
HSE,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
maternity,
Minister of Health Simon Harris,
pregnancy or infant loss,
TV3News
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Tuesday, 18 October 2016
Our Wave of Light for Isabella and all angel babies worldwide
As today is International Babyloss Awareness day, we are taking part in the International Wave of Light this evening. As bereaved parents ourselves we join the many other parents of angels from all over the world in lighting a candle for all our angel babies who have changed our lives forever. Today we honour and remember our babies in heaven and let them know we are thinking of them always. Isabella is our daughter in the sky and we miss her so much, love you Isabella with all our hearts xox
Labels:
angels,
baby,
bereavement,
chd awareness,
international wave of light,
NILMDTS,
Now I Lay Me Down To Sleep,
october pregnancy and infant loss awareness month,
pregnancy or infant loss,
waveoflight2016
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Letter to Minister for Health Simon Harris
Below is the letter I have sent to the Minister on 5/10/16, I have yet to gain a response however I have amazing people supporting me who are doing everything in their power to push for this crucial meeting that without a doubt must take place.
I will continue to keep everyone updated on our progress and will continue to drive our campaign this as much as possible.
Mother to an angel xox
Labels:
chd awareness,
child health,
Cllr. Damian Quigg,
Dail,
Dublin,
health,
HSE,
maternity,
Minister for Health Simon Harris,
neonatal,
pregnancy,
pregnancy or infant loss,
TD Louise O'Reily
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Friday, 14 October 2016
International Wave Of Light
October pregnancy and infant loss awareness month
Light a candle on Saturday 15th October at 7pm to honour all angel babies
As October is pregnancy and infant loss awareness month, we as angel parents are taking part in the 'International Wave of light' event and would like to invite all our friends, family and all those who have gained an angel baby or child.
Lets shed some light to create awareness and support to those who have walked the same path as us of loosing a child, lets honor and remember our beautiful angels in heaven, please join us by lighting a candle tomorrow (Saturday 15th October) at 7pm (GMT) for at least one hour.
Join people worldwide to help create awareness by posting a picture of your light on your facebook page and share with us on our Isabella's campaign by clicking here and remember to include hashtags #internationalwaveoflight #waveoflight #angelbabies #nilmdts
Let us together send light to our angels
Mother to an angel xox
Labels:
angels,
bereavement,
international wave of light,
Ireland,
isabella,
NILMDTS,
october pregnancy and infant loss awareness month,
pregnancy or infant loss
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
Wednesday, 12 October 2016
A brother’s love for his dying sister – how to explain the inevitable to siblings
Many people have asked me, how we handled our son Keelan
when the doctors told us about Isabella, and the answer I always give is we
were honest with him from the start.
I suppose the hardest part was knowing that Keelan already
said hello to his sister and that we told him already that his sister was
coming home that Friday, he was so excited becoming a big brother, I remember
sitting on the bed with Keelan after he saw Isabella with his dad when the
doctor and nurse came into the ward and asked to see myself and Kevin in a private
room, my heart sank as I knew there was something serious wrong by the look on
their faces, I looked at Keelan and he had the biggest smile on his face not
knowing what was happening, that is what
gets to me more about her heart condition not being picked up, our son had to
suffer the rollercoaster ride of emotion, something no sibling should ever go
through.
After we were told that she appeared to have complications
with her heart and that she was being sent to Crumlin, we were in a state of
shock, how could our precious baby girl who looked perfect and healthy have something wrong with
her? How serious is this? Is this life threatening? How are we meant to go out
of this room and explain to our son what is going on? Is he going to
understand? All of these questions were running around in our heads, I wanted
to go with her in the ambulance but I was not aloud after surgery, Kevin had to
go up alone in case paper work had to be signed but I don’t want him to be
alone and I don’t want my baby girl to not have her mum next to her. You simply
cannot process anything, all I knew is that I had to be truthful to Keelan, he
is 7 yrs old and has a good understanding about life itself, I strongly believe
as it was his sister he had the right to know the truth, if I tried to sugar
coat this it would be so much harder for him to process if anything was to
happen which at the time I would of never dreamed of.
We sat Keelan down and I said that the doctors have found
that Isabella’s heart is very sick and they are going to send her to a very special
hospital in Dublin where they are going to do everything they can to make her
better, but there maybe a chance she may fly with the angels. It took all my
strength not to collapse on the floor in front of my son, but if I looked
strong, he will be strong, he replied and said ‘ok mummy, I will say a little
prayer for my sister to get better so we can bring her home. As I stayed in
Kerry hospital for the next two days I spent as much time as possible with him
as I knew once I get to Dublin I wouldn’t know when I would be back down, the
night before I left my mum brought him down and I asked for her to go back to
my house to collect more stuff and to leave Keelan with me, that was quality
time we needed and time which became so important to ensure that he understood
what was going on.
I remember months prior to having Isabella my granddad (Keelan’s
great granddad) was very ill with cancer, I knew I had to prepare Keelan for
the inevitable, we visited him in the hospital but once he really started to deteriorate
I didn’t have the heart for Keelan to see him anymore, I wanted him to remember
him looking well and able to crack his jokes as always. To prepare Keelan I got
him a book about life and death so he would have a greater understanding for
the sad time that I knew was upon us, this really did help him, however I never
knew that this would be of use to help him through losing his baby sister.
Keelan came up on the Friday with all of the family,
amazingly Isabella gave us precious time so that Keelan had a chance to say
hello again and give her cuddles and kisses before she grew her wings. She was
christened at 4pm and we had a private photographer from NILMDTS to take photos
of her later that evening in her final hours with us, photos of Keelan holding
her, and our little family altogether which will forever be cherished, making those
memories that will now last a lifetime.
Isabella passed away early Saturday morning on my chest, we
brought her down to Kerry for her burial that same day, we brought her down to
Kevin’s dad house in Killorglin, so many people were there wanted to pay their
respects, Keelan wanted to help his dad place her in her little pink casket,
something that I would never expect for him to do but he wanted to, a sense of
a duty being her older brother. She layed there just looking like she was
sleeping, so beautiful and at peace, that was when it finally sunk in what had
happened, myself, Kevin and Keelan broke down together holding each other so
tight, a bond that will never brake. We did choose for Keelan not to attend Isabella’s burial as he had
already been through so much at this stage we felt that he said his goodbye’s
and now it was our turn to say goodbye.
Kevin walked out of his dad’s house holding little Isabella’s
casket so tight in his arms, while I walked behind him, the sun shining down on
us, the clouds were so fluffy in the sky, the river was sparkling and so many
swans gathered around the water’s edge, now it was time for us to say goodbye
to our darling Isabella.
I wanted to share this as I feel it is so important to see
from personal experiences how we as parents dealt with a situation that was
thrown to us, everybody has their own ways in parenting, but I just wanted to
show that being truthful to our children is the best way for them to learn
about life and death and how they begin to process this in their own way. We
all want to protect our children from pain and never want to see them cry, but
I think if we tell them nothing bad is going to happen and it does, it could
create a full sense of confusion and leave them thinking negative thoughts
about every situation they are told 'everything
is ok, and you don’t need to worry’ but if you sew the seed of maybe this
could happen but they are in the best care possible, this not only tells the
truth but also adds a percentage of preparing for the worse. This can be
relating to any family member, friend of family or even the families pet.
I like to say ‘preparation is key’ and it is especially for
siblings in circumstances like ours, this is why our campaign is so important
to get through to the Minister for Health that if Isabella’s heart condition
was picked up, and knowing that she could not of been saved we could of prepared
Keelan for the worse, however because the resources are not available to us
within the hospital our son said hello to his healthily sister then days later
goodbye, if that is not confusing I do not know what is and all because our
health system failed us. We know our Isabella could not have been saved,
however we want to save any other parents from the heart break of what we have
gone through.
Mother & brother to an angel xoxox
Labels:
chdawareness,
grieving siblings,
how to explain death to children,
HSE,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
NILMDTS,
pregnancy or infant loss,
remembrance photography,
sibling bereavement
I have two children one of which gained her wings and became an angel at 6 days old. My mission is to create awareness for congenital heart disease (CHD) and promoting better screening for all ladies who are pregnant.
We want to help any other parent who's child has CHD or who is walking the same path as ourselves of loosing a child.
Our angel Isabella was sent here for a reason and I believe her story will do just that.
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