A Stitch In Time Memories
105 Pinehill Drive L0R 1P0 Hamilton, ON, Canada

Brittany is your girl for stuffed balloons in the Hamilton area! She’s amazing!!

This about sums it up!

Always make sure you look beautiful, even in a lockdown here’s my simple everyday look. #makeuptutorial #maybeshesbornwithit #alianhandsydrome I challenge you lot, do it with the kids, husband, dog or if your on your own without the use of your hands! xxx LADbible

So grateful to the men & women who sacrificed for our freedom. Thank you.

EDIT: Tune into CHCH TV tonight at 6pm! We need our voices heard and they have given us a platform tonight! Justin Trudeau Christine Elliott Tonight is one tho...se nights that I lie awake in my bed and scroll through pictures...pictures of my 13 yr old Ella who since birth was spunky, strong, brave and hilarious child. Ella was diagnosed with #cysticfibrosis at the age of 5 months old after we almost lost her. Little did we know we would come close three times in her 13 yrs to losing her. She has had 7 surgeries so far, countless xrays, blood work, hospital clinic days, hospitals stays (twice this year alone) picc lines, her intestines coming out of her bellybutton with an ostomey, antibiotics, prednisone...you name it we have pumped it through her little body. When she was younger and didn’t know any better she thought it was a super power. Probably because she had jolts of energy after inhaled treatments. We have become family with the staff at #mcmastersickkids The staff at MAC have guided us step by step through fighting this battle as a family and they have joined us many times over the years to raise awareness and funds for research. Efforts that have gone so far as to find not one life changing medication, but several, including the giant of them all #trikafta. This past year, at the young age of 13, Ella has started questioning how long she will be with us. Ella’s lung functions has gone from 105% down to 58%. Her first diagnosis of CF we realized that she would struggle her whole life to breath and now along with the drop in function we have found out that the air she struggles to breath, she is also allergic to. So to fight, Ella’s body has been pumped full medications almost a year straight on top of the daily preventive therapies she has been on since 5 months old. We aren’t talking about amoxicillin, we are talking about hard hitting medications of antifungal drugs that cause severe liver damage, several antibiotics that have cause nausea, vomiting, rashes. The worst of them all being Prednisone, a drug that people should never be on long term (3months) and Ella has now been on that since January with no end In sight. All of this just to keep her slightly above the PFT required for a lung transplant. Imagine your daughter needing a lung transplant not because she choose to harm her lungs but because she born this way?!?! How is that fair to a child? Ella was a competitive swimmer, a bike riding, active, happy kid. The last 10 months I have seen her struggle to breath just going upstairs, have anxiety attacks when a friend wants to stop by for a distant visit in the driveway because of the swelling that happens on prednisone for so long, she’s moody, insecure and miserable because she has to fight to breath...and now I have to answer her question: Why bother with all these pills and treatments if they aren’t working? I’ll tell you why Ella, because I can’t be here on earth without you, so please for the love of god keep fighting and being compliant Ella’s light is dimming, for no other reason than you don’t think her life or the life of the 4,300 Canadians living and fighting #cysticfibrosis is worth the money...More than 20 other Countries have successfully negotiated with #Vertex for access to #trikafta and #canada won’t even come to the table. Disgusting. Tonight when you say goodnight to your Ella, know that you are killing mine with every second, every minute and every hour that you choose not to make the changes necessary for this drug to come Canada for it’s citizens with #cysticfibrosis. Sleep with that thought in your head Mr. Prime Minister, you have the power to make a change in CF patients lives and yet your keeping your head in the sand. What kind of leader does that? I doubt you will ever see or read this but for me, I need to know that I tried, that I have fought for Ella and the patients and families that fight every day against Cystic Fibrosis because apparently their government is happy to live in the land of ignorance all for the almighty dollar. Do something! Make the change! Get #trikafta in Canada, give CF’ers a fighting chance!!! CHCH CP24 Toronto's Breaking News CTV News Cystic Fibrosis Canada Conquering CF in Canada CF GET LOUD | Community #ellacantwait #cfcantwait Patty Hajdu

How cute is she! I had to share!

The past year has been a tornado of ‘things’ and I can’t get caught up. Too much has happened. I am working on the orders from the past year that I have on hand. I can’t not say when or if I will be accepting orders in the future. My personal life has completely changed and it is extremely hard for me to keep going at the pace that I was going. I wish I could help everyone but I am just one girl. I am so sorry to those I am letting down who have been patiently waiting on me. I am very overwhelmed and honestly can’t keep up.

NEW signs released today! PM to reserve your date!

Happy Birthday Andre!!