Reflections of a babywearing consultant and mother

Four years ago today I had just been discharged from Ward 8 of the University Hospital of North Durham, also known as ‘labour ward’ or the delivery suite.

Four years ago today I had just been discharged from Ward 8 of the University Hospital of North Durham, also known as ‘labour ward’ or the delivery suite. I had been there since 11am after being sent as an emergency by my community midwife following a routine 33 week appointment that morning. I had spent the previous evening and most of the night in agony. My bump tightening and feeling very sick. I had barely slept. I couldn’t eat. I felt, as the ‘On this Day’ feature of Facebook tells me, “like death warmed up”. 

Today it is Mother’s Day and I am blessed to be the mum of two beautiful boys and a loving husband. They have spoilt me rotten today.

  

Baby C thankfully did stayed put. The tightening’s continued and I spent most of the next 5 weeks on bed rest before ‘nesting’ kicked in at 39 and a bit weeks. Isaac was born at 40+5, a Born Before Arrival birth in just 18 minutes, he has been a whirlwind ever since. He is my carried baby. He is the one I carried from 8 hours old. Carried when he couldn’t feed, carried when breathing difficulties associated with Obstructive Sleep Apnoea meant he couldn’t breathe, carried as he recovered from countless chest infections and medical procedures, carried following surgery and carried to keep him close when he was scared. He is a definite ‘mummies boy’.

  

But Henry, carried for the practical reason of walking the dog is just as loving. This morning, he came downstairs, got a bowl, filled it with Special K and milk and carried it carefully upstairs to give me ‘breakfast in bed’. Nobody told him to do it, he came into the bedroom silently. I didn’t even know it was there. Unfortunately by the time I did it was inedible. But that isn’t the point. He did it for me, because I am his mum, because he loves me. He might be a true boy, rushing about at 100 miles an hour. Off without a second glance when we get to the school yard each morning but he knows I am there. From the little quick kiss that he plants on my forehead then walks away, or the hand he puts on my lap when he thinks no one is looking, they are his way of saying that I mean something to him. He made me a mother. He and Isaac have shaped my very being since the minute they were created.

 

Without them I would not be me. I am not just Henry’sMummy (my username on many a forum) or Henry and Isaac’s Mummy. I am Rachel but being Henry and Isaac’s mummy is a very big and special part of me.

Without them I would not be me. I am not just Henry’sMummy (my username on many a forum) or Henry and Isaac’s Mummy. I am Rachel but being Henry and Isaac’s mummy is a very big and special part of me.

The day before Isaac’s attempted arrival I had completed my first every babywearing consultation. I had finished my Trageschule Foundation course just 28 hours before. I had travelled nearly 600 miles in 4 days, completed a 2 day course and then a 90 minute consult (it was during that the pains started). And do you know what? I wouldn’t change it for the world. I completed my last consultation just 11 hours before he was born and restarted them just 3 weeks later.

I had finished my Trageschule Foundation course just 28 hours before. I had travelled nearly 600 miles in 4 days, completed a 2 day course and then a 90 minute consult (it was during that the pains started). And do you know what? I wouldn’t change it for the world.

I am honoured to be a carrying or babywearing consultant. I am honoured that so many Mother’s and Father’s let me into their homes, or come to mine, let me hold their precious bundles, their miracles of creation, carry them and show them how to do carry them too. Whether they are their biological children, the result of IVF, surrogacy or adoption, they are all special, they are all unique. Each family is unique. Each set of circumstances unique. I have completed hundreds of consultations since then. Thousands of hours are spent dedicated to helping each family, before, during and after their appointment. My own children are often the ones to suffer, while I answer the phone or an email. They want me but I know others want and need me too. It is a balancing act that I am still mastering.

  
 Four years since I qualified as a babywearing consultant I have gone on to complete 3 more consultancy training courses, I have grown my sling library, I have stopped teaching, I have become solely self employed with all the ups and downs it brings. I have shown strength I didn’t know I had. I have cried tears of joy and sadness. I have spent sleepless nights worrying about families and hoping that I have made their lives just a little bit easier. I am truly thankful for the life that my children have allowed me to lead. Without them and their need to be carried, I would not have found slings. I would not have found the mamas who shared their knowledge with me, I would not have found something I have a passion for and a belief in. Thank you to my boys, my husband and the hundreds of families who have asked me to help them. Thank you to my Mum, who is the reason I am here.

Happy Mother’s Day everyone. I hope you have enjoyed it. I hope you have been spoilt and I hope you have many, many more to come.

Carrying and its role in Toby and Teddy’s lives

The next in our blog series on carrying children with additional needs is written by Rachel. She is a mum of two boys and lives in the North East. Her eldest son was diagnosed with Autism just after his second birthday. Autism is a spectrum disorder and those with the condition can vary in severity. Autistic Spectrum Disorders are a “condition that affects social interaction, communication, interests and behaviour”.  Difficulties in communication and social interaction can have a massive impact on families. Carrying Toby, and his younger brother Teddy, has allowed Rachel and her husband to adjust. I will let Rachel take over now. Continue reading

The Tired Mummy Chicken Pox Survival Kit

img_1877Isaac has Chicken Pox! It has been 3 years since the pox last hit our house. Henry had it in the summer so we basically lived in the garden for a week. Unfortunately, it is a tad too chilly in February to be spending our days in the garden. The pox has been at nursery for a few weeks but up to now Isaac had avoided it but not anymore! I got the phone all from nursery yesterday afternoon to say could I collect him. This morning it is very clear that it is Chicken Pox.

Henry took chicken pox in his stride. He was happy as long as he wore a long sleeved cricket top and a fleece jumper.

Isaac on the other hand is Isaac. Nothing is ever plain sailing. A 15 minute battle to put camomile lotion on is testament to that. I have a feeling it is going to be a very long day, especially as Henry and Daddy are off to watch the new Star Wars movie after school. Typically the pox has arrived when Martin and I had plans for the weekend – tickets for the Calcutta Cup (Scotland v England) in the Six Nations Rugby.

So here is my survival kit and how I intend to cope over the next few days: plenty of tea, antihistamine, infant paracetamol, calamine cream, slings (my Opitai and preschool Connecta Baby Carrier Solar), suck pads for the straps of the carriers, my Boba Hoodie and copious amounts of chocolate, oh and the TV/iPad.


The antihistamine, calamine cream and the infant paracetamol are to help treat the Isaac’s symptoms. The antihistamine and calamine cream to stop the itching, and the paracetamol to treat his temperature. The slings allow me to care for his needs and want to be held. When children are poorly they want and need comfort. The Opitai is a custom size wrap conversion and the Connecta is made from the lightweight Solar fabric. Both are soft and non-irritating on his already “scratchy mummy” skin. The Boba Hoodie allows us to walk the dog and get some fresh air (yes I am as tired as I look) while both staying warm. He is refusing to get dressed in anything other than the fleece pyjamas he got for Christmas. The chocolate and tea are for me (although he has already spied the chocolate). The iPad and TV are keeping him entertained and helping him to forgot that he wants to scratch. The car will probably be coming into use too so that I can get him to sleep (he is pretending in the photo of Boba Hoodie).

 

What is your top tip for coping with Chicken Pox? I’d love him to have an oat bath but so far the idea of him going in bath or shower is apparently abhorrent.

Gideon’s Story

This piece is the third installment of our series looking at how babywearing and carrying is more than just being about the sling and how it can help families who have babies and children with additional needs. It is written by Rae, a Mum of Three. I have ‘known’ Rae for the majority of my own carrying journey as we are both members of the Natural Mamas forum and we shared our own pregnancy journey’s on its pregnancy sub forum. Here Rae will explain how using a sling helped her care for and bond with her third son. When Gideon was born he was diagnosed with Prader-Willi Syndrome or (PWS). 

At birth babies with PWS are usually very floppy (hypotonia) and this means they often cannot suck properly, have a weak cry and often do not have a full range of movement. It is a genetic disorder that is typically not diagnosed until baby has been born, although lack of movement in utero can be associated with the condition. There have been research studies undertaken to investigate if fetal ultrasound scanning can be used to help diagnose the condition but currently 99% of cases are diagnosed via genetic testing.

Continue reading

How carrying helped one child with Juvenile Arthritis.

The next blog in our series of carrying babies and children with additional needs is written by Kirsty. I was lucky enough to meet Kirsty quite early on in her carrying journey as she visited the sling library for help and support. In 2014, her little girl was diagnosed with Juvenile Arthritis. born to carry.jpgSince Olivia’s diagnosis Kirsty has trained as a babywearing peer supporter with Born to Carry.

Juvenile Arthritis is an umbrella term that is used to describe “many autoimmune and inflammatory conditions or paediatric rheumatic diseases that can develop in children under the age of 16”(http://www.arthritis.org). Diagnosis can take several months.

In this blog Kirsty explains how babywearing has helped her care for Olivia as well as details of how she was diagnosed. Thank you for sharing your experiences Kirsty.

I will let Kirsty take over her story here: Continue reading