The Spider-Ede Appeal

Raising funds and awareness of DIPG

Donate
Facebook
Twitter
Instagram
YouTube
Merchandise

Search for:

Menu

Home
About Pages +
News & Events
Fundraising
Upcoming Events
Contact Us
Thank You Pages +
Merchandise +
- Purchase Merchandise
- Photo Gallery

Spider-Ede Children’s Christmas Party

Posted on November 13, 2018 by Spider-Ede Leave a comment

Christmas Party Poster

🎄Come and join the Christmas fun!⛄️

For just £7 per child there will be a grotto with a gift, disco, children’s buffet and so much more!

Don’t forget to dress to impress, you could win the Christmas outfit competition!! 🎉🎁

St. Joseph’s Social Club, Birkenhead, 16th December, 12-3pm

Contact Hazel Anderson on hazel@spider-ede.org.uk to book tickets.
❤️🕷💙
#Fight4Edie #DIPGAwareness

Share this:

Click to share on Twitter (Opens in new window)
Click to share on Facebook (Opens in new window)
Click to share on LinkedIn (Opens in new window)
Click to share on Pinterest (Opens in new window)
Click to share on Pocket (Opens in new window)

Like this:

Like Loading...

Related

tagged with christmas, Fundraising

Events

Leave a Reply Cancel reply

Enter your comment here...

Fill in your details below or click an icon to log in:

Email (required) (Address never made public)

Name (required)

Website

You are commenting using your WordPress.com account. ( Log Out / Change )

You are commenting using your Google account. ( Log Out / Change )

You are commenting using your Twitter account. ( Log Out / Change )

You are commenting using your Facebook account. ( Log Out / Change )

Connecting to %s

Notify me of new comments via email.

Notify me of new posts via email.

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Donate Online

Upcoming Events

We have no events planned at present.

To view our full calendar of upcoming events, visit our Upcoming Events page.

Other ways to Donate

The Spider-Ede Appeal – DIPG Awareness

The Spider-Ede Appeal – DIPG Awareness

Latest

Recent
Popular
Comments

Celebration of Life Video
January 16, 2019
It’s the little things
January 8, 2019
Update – December 23, 2018 at 04:06PM
December 31, 2018
Update – December 12, 2018 at 12:25PM
December 17, 2018
Visiting Santa at the Craft Fair
December 1, 2018

Running for Edie
January 3, 2018
Buy a Spider-Ede Bracelet
December 22, 2017
New YouTube Channel
January 2, 2018
Race at your pace challenge
January 1, 2018
Positive News from Mexico
February 12, 2018

Lucia aguiñaga Rodríguez on Fly High Edie May
Lynn on Update – 21st October
Final Call for Spider-Ede’s Ball Tickets | The Spider-Ede Appeal on Spider-Ede’s Birthday Ball
Postponed: Greg’s Sponsored Climb | The Spider-Ede Appeal on Heroic Endeavours
BEZ on Spider-Ede Rocks!

Follow The Spider-Ede Appeal on WordPress.com

Upcoming Events

No upcoming events

Instagram

These past few weeks have been tougher than usual, even for us. Edie’s little brother Len, who is 2 and a half, started to complain his head was hurting. You cannot imagine and we couldn’t fully explain to you how this has made us feel 💔 In July 2017 at the same age, Edie first started to complain of headaches. Over that summer, we assumed it was dehydration and kept topping her up with fluids more regularly. Her headaches progressively got worse, lasting longer and were more frequent. Our visit to the family doctor ended up with a referral to paediatrics, just as a precaution, and then another referral from there for an MRI, again “just in case,” to then be told that Edie, our otherwise healthy little girl, had a fatal brain tumour DIPG and that she would have around 9 months to live 💔😢 And now, we have just had to relive the beginning of that nightmare. Len has had to go through all of the same tests as Edie did, including being under general anaesthesia for an MRI scan, which brought back so many memories of holding our girl in our arms while she drifted off before surgeries ❤️💙 Because of Edie and that now we do have a family connection to brain cancer, the radiologist was extra thorough. After what felt like a lifetime anxiously waiting and seriously expecting the worst, Len’s results were brought back to us in the afternoon. His scan was all clear with everything looking normal. We are relieved and exhausted. And we’re left questioning if we will ever not be stressed about our children’s health. After all, that monster was lurking in our daughter’s head for how long we don’t know but we couldn’t see it. Has going through DIPG with Edie changed us? Yes, it has. We see how fragile life is. We have spent the last few weeks watching Len play and imagining him disappear before our eyes. Would we say we are less positive? Less hopeful? Probably. Look what we have been through. It is so much harder to see the bright side, to not worry about our children. And did we feel like we were being silly, paranoid, over cautious? Yes, but we left Edie’s symptoms for over a month thinking they were dehydration or wanting to stay off nursery. We will never again be ab

We now believe Edie is watching over us, has sent us this blessing and she would be so pleased to have a new little brother. She loved babies and was such a fantastic big sister to Len. That is not all. As you know, we were supported by the Bradley Lowery Foundation. Well this hasn't stopped. Like the fantastic people they are, they offered us an amazing opportunity to keep Edie's legacy alive. We have remaining over £100k in Edie's account with BLF. And we know Edie would want us to try and find a cure for DIPG. So that is what we are going to do. Working closely with BLF, Researchers and Consultants, we are looking to use the money already raised as well future fundraising, to fund vital research into DIPG, in the hope that one day, we can cure our babies. We don't want any other family going what we are going through now. Edie will always be remembered for her big smile, mischievous attitude, and most importantly, the awareness she raised for DIPG. We hope you will all carry on supporting, and together we WILL find a cure 💪🙌🙏 💙🕷❤️ #DIPG #EdiesLegacy #DIPGAwareness #EndDIPG To donate directly into Edie’s DIPG research fund: Visit www.justgiving.com/campaign/spiderede

We know we haven't really done any personal posts for a while, as you can imagine, it has been and still is, extremely hard for us all as a family 💔 We just want to give you a little update, you all helped us so much get Edie treatment to try and save her, we feel that it is only right to let you all know how we are all doing and what our future plans are. Myself and Steve have taken time out, and we didn't really leave the family home much becoming quite unsociable and reclusive. We didn't know what we were doing, how we felt or how we were supposed to feel. If we cried we felt guilty, if we laughed we felt guilty, we have found it easier to stay in and limit who visited to close family that need no communication 😢 We've had time with Niamh and Len just the 4 of us. We missed so much of them when Edie was having treatment, but they both took it in their stride, adapting so well. They are so grown up for their age. Niamh is always talking about Edie, she draws pictures and writes notes for her, makes little bracelets to put on her hand cast. If we are doing something fun, she will say, “Edie would love doing this Mummy” And shes right, Edie loved life, and she would want us all to live our best lives now. Len is, well being Len. He has no fear just like his big sister Edie. We see a lot of her in him, especially the cheekiness and how he just knows how funny he is. He is still too young to understand fully what we have all been through, but we always talk about Edie, he sees photos and shouts her name, we know he will always remember his brave, funny, beautiful sister❤️💙 We are starting to look to the future without our little girl, and it is so hard, we know there will be good days and bad, but we are now a little more prepared and know it’s ok to have a bad day. We also have a little bit more news for you all. We are expecting another baby to join us towards the end of this year. We were shocked at first as it did take us by surprise. We have been through a rollercoaster of emotions from feeling horrendous guilt that we are somehow replacing our girl to feeling so blessed that we have been given the chance of something happy. *continued next post*

Day 17 of running 40-60 miles!! He’s on the final leg of his epic journey!🏃🏻‍♂️🏃🏻‍♂️ Super John Hammond is almost finished running the length of the UK! 🇬🇧 He’s already ran more than 800 miles over the consecutive days, which is unbelievable!! “Think everyone knows how much I’ve struggled through this and I have absolutely no idea how I’ve nearly got through it. I don’t even think it’s down to having a strong mind this time. I think it’s down to sheer madness” John, this morning as he started his last 50+ miles. John has almost reached his fundraising target for his 5 charities, we ask you all to please dig deep just as he has to complete this challenge and give him a massive boost by donating as much as you can to help him reach his target! 🙏🙏🙏 Well done John, last push and you are there! You truly are a hero! 🙌 www.justgiving.com/crowdfunding/helphammo Here are some photos of John with our family, the support he has always shown us is unwavering and we are so proud of him as we know Edie would be. 💙🕷❤️

"If a drug company came up with a drug for DIPG, it would take them 10 years, and cost them 100 million bucks, and they would treat 15-to-20 kids a year - so there is no return on investment for them," Dr Dun said. This quote is taken from an article published in the Newcastle Herald online, Australia. Our question as parents, families, communities is are our children not worth the investment??? #EdiesLegacy #DIPG #DIPGAwareness #EndDIPG #ResearchMatters To donate directly into Edie’s DIPG research fund: Visit JustGiving.spider-ede.org.uk

🏅Keep going John🏅 Super John Hammond is running the length of the Uk to raise money for 5 local charities! John o’groats to Land’s end, 874 miles! 🏃🏻‍♂️🏃🏻‍♂️ He’s over half way and doing amazing! Running around 40-60 miles a day 😱 Today we got up early to chase him down and cheer him on before school! We are incredibly proud of you John and feel so lucky to call you a friend! 🙌👏 We’ll be keeping track of John’s progress and you can too on his twitter account @johnammo29 You can also show John your support by commenting some words of encouragement or donating at www.justgiving.com/crowdfunding/helphammoeverystep

🌟Raffle time🌟 As you all know, we are continuing to raise funds to help with DIPG research, in the hope that one day a cure is found and families no longer have to go through the heartbreak of what we have❤️ This means events will occasionally take place and we have one this Sunday! Our past boat trips have been a hit, the weather is hot and dry in the evening, what better way to spend it than sailing up and down the Mersey with a live band and a drink in hand. ⛴🎤🍻 We are raffling off 2 pairs of tickets for just £1 per entry - 2 chances to win! 🎟 🎟 If you would like to enter, please comment below and we will message you with payment details. Raffle will be drawn on Saturday evening! ❤️🕷💙 JustGiving.spider-ede.org.uk www.spider-ede.org.uk #EdiesLegacy #DIPGAwareness

The last 7 months have been awful. After we lost Edie we had many well wishes, cards, letters, gifts, notes. At the time we couldn’t read them 💔 Today we pulled the rainbow bag out that Iwe had “shoved them all in”. We’ve only managed to read 3 properly but feeling so overwhelmed with love. We know that over time we will read through them over and over. The shoes you see in the corner are Edie’s favourite old shoes, hand-me-downs that she loved to wear on the wrong feet 🙈 they ended up in the bag as we sorted through some things and decided we wanted to keep them and somehow get them box framed 😍 We didn’t acknowledge anyone that sent us these things and we know you didn’t expect any recognition but we do want to say THANK YOU. It is a massive comfort knowing the love our girl has. ❤️🕷💙 #EdiesLegacy #DIPG #DIPGAwareness #EndDIPG #ThisIsGrief To donate directly into Edie’s DIPG research fund: Visit JustGiving.spider-ede.org.uk

You all remember our fantastic John Hammond, Wirral’s local “running man”. Today he set off again on one of his crazy fundraising challenges. He is running the length of the Uk from John O’Groats to Lands End!! 🗺 🇬🇧 Totalling 860 miles and he’s hoping to get it done in 17 days. Running around 40-60 miles a day! 🏃🏻‍♂️🏃🏻‍♂️🏃🏻‍♂️🏃🏻‍♂️ John is raising money for 5 great local charities listed below for you all to take a look at what they do. We’ll be keeping track of John’s progress and you can too on his twitter account @johnammo29 You can also show John your support by donating at www.justgiving.com/crowdfunding/helphammo Well done John on your first day, 37 miles in the bag! 👏💪 we wish you the best of luck and know our girl will be watching over you all the way ❤️🕷💙 Mind- www.wirralmind.org.uk Local specialised support for anyone experiencing a mental health problem. DIPG Awareness- The Spider-Ede Appeal spider-ede-appeal.org.uk and Lucy’s pineapple fund www.lucypineapple.co.uk Raising funds for awareness and research into DIPG. The Paul Lavelle Foundation- paullavellefoundation.co.uk Raising Awareness or Male domestic violence and supporting victims and families affected. Claire House Children’s Hospice- www.clairehouse.org.uk Helping seriously and terminally ill children. Supporting better quality of life Charlie’s Chance-www.charlieschancefoundation.org Offering emotional and financial support to local children and their families affected by cancer. #Hammo #RunningMan #CharityHero #JOGLE

Tags

300 alder hey anfield ann summers appeal avengers awareness baking bingo birkenhead Birthday Ball bracelet breaking news burlesque cake cancer cartoon charity child friendly christmas collecting crafts dipg donation donations edie family family friendly featured fight4edie food funding Fundraising gift head shave hospital icu interview ladies night lfc liverpool madhouse media medical merchandise mexico monterrey mri scan music nativity News pantomime party press radio raffle Research running scan results school shopping social media softplay spider-ede spider-man sponsored sports superheros thank you tranmere treatment update video vlog Wirral

Follow The Spider-Ede Appeal on WordPress.com

Please note that as an Amazon Associate I earn from qualifying purchases.

Privacy & Cookies: This site uses cookies. By continuing to use this website, you agree to their use.
To find out more, including how to control cookies, see here: Our Cookie Policy

%d bloggers like this: