Showing posts with label pregnancy or infant loss. Show all posts
Showing posts with label pregnancy or infant loss. Show all posts
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.
Saturday, 12 November 2016
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.
Sunday, 18 September 2016
Campaign Update
Last week since the initial launch of our campaign Cllr. Damian Quigg contacted me after he saw my interview on TV3 News, he explained that through his election to Kerry County Council he gained a position on the 'Southern Health Board' and is fortunate enough to be able to raise our campaign at a higher level.
It has since been confirmed today that following the email I sent to Cllr. Damian Quigg explaining our Isabella's story, the facts around (CHD) and why it is vital that all expectant mothers should have a standardized 'free detailed screening', that he will be raising our campaign on Thursday 22nd September at the 'Southern Regional Health Forum' meeting in Cork. This is absolutely outstanding progress for the campaign and we could not thank Cllr. Damian Quigg any more for the amazing support he is giving us. Cllr. Damian Quigg will forward the response from the Health Forum to me next week so I will keep you all posted.
As in my previous post regarding the meeting I had in the Dail with Louise O'Reilly TD which
Cllr. Damian Quigg arranged while we were in Dublin, he advised that as the Dail is currently in recess that Louise O'Reilly TD will immediately seek to arrange a meeting with the Minister for Health Simon Harris, during our meeting it became very clear that this issue has been a talking point and that the Minister would want to learn more, I have made it very clear that I will be part of every step of the process to ensure that our voice is heard and the procedures we request are put in place.
During my visit to Crumlin last week I was very lucky to see Dr. Orla Franklin, literally in the corridor which was pure fate, (a little help from above I like to think). Dr. Orla Franklin was Isabella's Cardiologist and as I explained to her about our campaign she agreed with every word that was said, while she was talking she had as much passion as we do, it made me think that if these scans were put in place and proper arrangements were made prior to the birth then Crumlin would greatly benefit also as they do feel the immense strain when these emergency cases such as ourselves come in without any warning, doctors and nurses scrambling around trying their best to find out what is going on, planning the procedures and even delaying confirmed surgeries to save a life, a life of a baby. I strongly believe that Dr. Orla Franklin would be a great spokesperson from a medical stand point, she understands exactly what we should have put in place, she has seen these cases all too many times and I know her voice will be heard alongside ours.
So, that's all the news so far, to summarize we are waiting for a meeting to be confirmed with Minster for Health Simon Harris which Louise O'Reilly TD will be actively seeking once the Dail commences again, following on from that Cllr. Damian Quigg will be attending the 'Southern Regional Health Forum' meeting in Cork next week and he will send the response from that to me next week, so keep an eye out for more updates.
Below I have copied the email I wrote to Cllr. Damian Quigg, highlighting our campaign to present at the 'Southern Regional Health Forum'.
Dear Cllr. Damien Quigg
I am writing to you following up from our previous meeting in relation to the launch of our campaign for, CHD Awareness (Congenital Heart Disease) and to promote ‘Free routine detailed screening’ to all expectant mothers nationwide.
It has been found that (CHD) can affect one in every 100 babies, which is an incredible statistic knowing how many babies have previously been affected, with a large number of them only being diagnosed days after birth, decreasing their survival rate by more then half. As this is not a hereditary disease this means no previous health problems within the parent’s family history can indicate if such a disease could be possible. (CHD) is caused by a simple miss communication during the early stages of pregnancy, and can be diagnosed during a detailed 20 week scan.
As the heart being the most vital organ in our body, any such diagnosis must be referred to Crumlin during the pregnancy in order for surgeons to gain a clear understanding of the issues present and to outline a surgical plan to ensure all necessary arrangements are put in place upon birth. The mother would then have her baby in Dublin’s maternity hospital within the ‘Coombe’ which is located near Crumlin where the baby would be transferred immediately, however this was not the case for our daughter.
Isabella Eileen Sheehan was born by emergency C-Section on Monday 23rd May 2016 at 12.01pm weighing 5 Pounds and 1 Ounce. Myself and Kevin went to see her early that same morning in the Emly Ward, doctors present explained that everything was ‘perfect’ and they were just waiting for her to suckle before we could bring her home on Friday, our son Keelan who is aged 7 then went to see his sister, it was during this time the doctor advised that they detected a ‘slight heart murmur’ and they were running a couple of testes to make sure everything was fine. Approx 10 hours after she was born a doctor and nurse asked to see myself and Kevin in a private room and explained that her heart condition seems to be much more serious and that she will need to be taken to Dublin as soon as possible. As parents to be told that everything was fine, to the complete opposite we were absolutely devastated, more so that we had to explain the situation to our son who also suffers from ‘ADHD’. Kevin followed the ambulance and arrived in Crumlin appox 10pm that evening to be by our daughters side and to sign any paper work if an operation was to take place.
I had to remain in Kerry because of my C-section however I was told recently that Crumlin had arranged a bed for me in Dublin on the Monday evening but there was a clear miss communication within Kerry hospital to arrange transportation for me. I was later discharged on the Wednesday once I was able to be mobile and relatives arranged a car for the journey on that same day, while I still did not know what was happening with our daughter. The next day on Thursday morning we were told that Isabella had ‘Hypoplastic Left Heart Syndrome’ along with many other complications, they advised that because her heart was too complex that they could not even offer her surgery to save her. Isabella was christened the very next day on Friday and passed away in our arms Saturday morning, to which we then traveled with her back down to Kerry for her burial the same day.
We understand in Isabella’s case there was no possible way they could save her, however in a different circumstance if there was any chance of survival she could have well lost her life in transit on her way to Dublin because her diagnosis was not picked up and no procedures were put in place. Furthermore our surgeon in Crumlin explained that with ‘Hypoplastic Left Heart Syndrome’, there is never a heart murmur present which made Isabella’s case very unusual, only due to her further complications with her heart that this murmur was present, this would lead us to believe that if she had the ‘Hypoplastic Left Heart syndrome’ and no other issues with her heart the condition would not have been picked up after birth, and that we would of brought her home where she would of passed away unexpectedly, obviously causing us emotional distress.
As you can appreciate, Crumlin are already under immense strain and even more so when emergencies like ourselves come in, in many cases as serious as our daughters it takes time to investigate the full extent of the diagnosis and the planning process for surgical options. As Isabella’s heart condition was not picked up during her scans in Kerry, the Crumlin team had to start from scratch and the decision was not made until day 3 of her life. As a mother I feel I lost time with my daughter because I did not have her in Dublin were I would have been if this was picked up.
In respect of the HSE if these scans are put in place they would save an incredible amount of money as parents would arrange for their own transportation to Dublin instead of using the emergency services as necessary, along with many other resources used during an emergency situation.
Since my campaign I have received hundreds of emails from families who have also experienced the very same journey as ourselves with their babies being rushed to Crumlin for emergency operations. I am representing all of these parents along with future families that could walk the same fate as ourselves if routine detailed screening of all vital organs during pregnancy is not made essential within our maternity wards. In recent weeks I have learned that all expectant mothers in Dublin do receive these routine detailed scans, so my question is, why are not all expectant mothers nationwide entitled to them also? All vital organs must be screened to ensure that if anything is present, proper procedures are put in place upon birth.
Our babies are our future Ireland, and they deserve the best care possible upon birth.
I trust that you have gained some insight into our campaign and what our ultimate goal is for all expectant mothers nationwide.
Please do not hesitate to contact me if you require further information or if you have any questions.
Thank you,
Kind regards
Jazmine Sands & Kevin Sheehan
Labels:
chdawareness,
Crumlin,
Dublin,
HSE,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
Minister of Health Simon Harris,
pregnancy or infant loss,
scans,
Southern Regional Health Forum,
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.
Saturday, 17 September 2016
Corks RedFM Radio Campaign Interview
Since the launch of our campaign to raise awareness for (CHD) and to also promote 'free detailed screening' to all expectant mothers nationwide, we have had some amazing opportunities through the media to share our Isabella's story and begin our campaign's journey.
We would like to express our appreciation to all the media who listened to the true meaning of our campaign and the goal we aim to achieve.
Click Here to listen to my full Cork's RedFM interview, @ the time of approx; 021:00
Please feel free to leave a comment or click on our 'contact us' page if you would like to email us.
Thank you all for your support with our campaign and I promise that we will not stop until we are heard and 'free detailed screening' is offered to all expectant mothers nationwide here in Ireland.
Mother to an Angel
Jazmine Sands
Labels:
chd awareness,
Corks RedFm,
Crumlin,
Dublin,
health,
HSE,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
Minister of Health Simon Harris,
pregnancy or infant loss,
scans
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, 16 September 2016
Now I Lay Me Down To Sleep - Our photographer for Isabella
NILMDTS
Now I Lay Me Down to Sleep
Capturing Love, Not Loss
Once we were told on
that fateful day that there was nothing they can do to fix our Isabella’s heart
we did not know what to do next, in fact we were frantic as we knew time was
stolen, every minute we had her here we wanted to try and do everything we can
for our family and close friends to meet with her and capture every little
expression she gave us onto camera before she grew her angel wings.
As I have constantly said
throughout our campaign, the Crumlin staff has been and still are absolutely amazing
and truly gave us a little light at such a dark hour. They explained that they
can organize a christening for her and also a private photographer, I must
admit I was taken back a little of the thought of having someone come in and
take photos of our dying daughter or even if she had already passed away, as I
tried to think it through all that was going around in my head is that her big
brother needs pictures of her, we need pictures of her, this will be a once in
a lifetime opportunity, there would be no going back if we changed our minds
and if we did not like them then we don’t have to look at them, but my goodness
I am so pleased we went ahead and had them done.
Our photographer
Michelle came in and she was so respectful and instantly put us at ease, she
took photos of her little teddies, her hands and feet and then started to take
photos of our little princess with us by her side, Isabella was amazing and
gave us this extra time to get these photos done of her within her final hours.
There was a sense of calm while we were having our photos taken and it was as
if time was frozen, and now we can look back at these precious moments and have
a sense that she is with as always.

Her big brother keelan said ‘I miss my sister Isabella very much, she is still part of our family because we have these photos that the lady took of her’.
NILMDTS gave us a
chance to capture our daughter’s expressions and most beautiful eyes, we truly
feel blessed to have her pictures to look at, and we feel so grateful to know
that our son Keelan will have these to remember her by.
Photos by NILMDTS
NILMDTS Mission is to introduce Remembrance Photography to parents
suffering the Loss of a baby with the Gift of Professional Portraiture.
View their website here; www.nowilaymedowntosleep.org
NILMDTS facebook page click here
If you would like to volunteer to become a NILMDTS photographer or if you would be interested in learning more about various volunteer roles nationwide here in Ireland or worldwide click here to find out how to be part of this amazing organization.
Or if you know someone who needs the service of NILMDTS, please contact their central number
083 377 4777 or nilmdtsireland@gmail.com
A special thank you to our photographer Michelle and all at NILMDTS, you gave us a little light at such a dark time, you let us create memories and keep them for a lifetime and to that we thank you.
Labels:
baby,
HSE,
Ireland,
Isabella's CHD Awareness & Pregnancy Screening Campaign,
miscarriage,
neonatal,
NILMDTS,
Now I Lay Me Down To Sleep,
pregnancy or infant loss,
remembrance photography,
SIDS,
stillbirth
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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