Yvonne's Aloe Store

Back to school and back to dance!

Great time to start a new hobby.

Our classes have resumed in Balgriffin hall, and we will be back in Evolutis Gym on Tuesday 12th September.

New members always welcome.

Please like and share and help spread the word.

I think FB is not spreading my posts regarding this charity. It must recognise the number and these posts keep being seen by about 10% of my regular posts. And i Know you lot are Amazing and wouldnt be ignoring it...Some pics were even of the adorable kids and they are so cute..but Likes and who saw the post, were way down. FB kept offering to boost the post if i paid...well that defeats the purpose of raising money. So sharing it on, mite be the way to go and help Irelands ONLY kids hospice..i'll read the final total on Ireland am tomorrow. ☺😚😙😗😍

Come along to our new class in Evolutis Gym
Beside Iceland Tuesdays at 5.30pm or to Balgriffin Hall Malahide road Wednesday 5.30pm or Saturday 9.30am

***Exciting announcement***
Following an amazing weekend at the Irish Open championships it's back to class time.

We are delighted to announce we are expanding our class from Tuesday next 9th May with a new beginners class at 5.30-6.30 in the brand new dance studio in Evolutis Gym, Greencastle parade beside Iceland.
First class is free!

Contact us to register your interest or turn up on the night.

Classes continue in Balgriffin Hall Wednesday's 5.30pm and Saturdays at 9.30am with new dancers also welcome.

https://www.facebook.com/CarolanschoolofIrishDancing/

Grab a bargain!

Various aloe products reduced due to non collection of orders

**Propolis** €20.47 reduced to €17
**Sun cream** Sold
**Sun spray** €19.94 reduced to €16
**Gentlemans Pride aftershave** €16.72 reduced to €14
**Forever sun lips** X 3 €5.12 reduced to €4 each
**Moisturising lotion** Sold
**Aloe Vera gelly** €16.72 reduced to €14
Fabulous Sonya range:
**Serum** €46.52 reduced to €40
**Toner** X 3 €37.45 reduced to €30 each
**Deep Cleansing exfoliator** €28.09 reduced to €22
**Eye make up remover** Sold
**BB creme - n**e** €39 reduced to €30

Supplements
**Forever daily** €22.77 reduced to €20
**Forever therm** €39.48 reduced to €33
**Royal jelly** €37.10 reduced to €30

Please read this from Dylan's dad. If you can spare anything for a birthday donation for Dylan they would be so grateful x

A Birthday Wish from Dylan’s Dad – Dylan’s 4th Birthday is Today - Monday 3rd October. Please read and share my letter.

Hello,
My name is Alan Finglas - Dylan’s father, I am writing to you today for a couple of reasons. Firstly, I wish to THANK YOU from the bottom of my heart for your support since we started our campaign. Your kindness and thoughtfulness has made us believe we will succeed. Words could never do justice in describing how grateful my family are that you would help us to stop Multiple Sulfatase Deficiency and save Dylan’s life.

With your help we’ve come this far and your support has been overwhelming. At this point, 18 months into our journey to try and give Dylan a chance at life, we as a family must continue our struggle. Putting our story and our fight for life out there and into the public eye has taken its toll on my family but we will never give up, we can’t, it’s just not an option!

If you have been following SavingDylan on social media you will know we have rolled from one fundraising event to another. The initial goal we set out for our campaign was to raise 1M Euro from our fundraising efforts with the hope that 1M can be secured in grants. We hope to reach our goal a.s.a.p, and take one big step closer to the finish of our struggle, to give a chance at life to Dylan. We are now €466,000 short of our target. (We have raised €534,000 so far) - Please let me explain.

Dylan’s 4th birthday is Monday 3rd October. This is a critical time in the life of most children with MSD and Dylan has started to lose skills. It’s been heart breaking to see the changes over the past year, but we can halt this devastating condition and soon. We all love birthday celebrations but for us that’s not exactly the case. For our family, each birthday is a marker in time where we fear a decline that will continue if something doesn’t happen soon. We wonder what Dylan will be like if/when he reaches his next birthday.

We hope to focus and enjoy Dylan’s ‘good days’ with him as much as possible as the future still remains uncertain. Dylan needs more of our attention and care to try to keep him active and mentally stimulated, and less of seeing his parents working on the computer, making calls, promoting MSD awareness and trying to organise fundraising events.

We must push ahead with the excellent scientific breakthroughs on MSD. The alternative is just too painful to think about. The step by step approach we’ve taken so far is robbing us of precious time that we could spend together as a family. We live on hope every day, people wish us well and even offer prayers for us. Although hopes, well wishes and prayers are nice, ‘Action is what we need’ it will make the difference. You have already shown us action by helping, sharing and donating to our cause.

We are potentially only a few months away from a treatment. Thanks to you, a drug product (medicine) for children with MSD is being tested at a pre-clinical stage to seek proof of concept on human MSD cells. A potential trial for this (it has already stopped a similar condition to MSD!) along with other promising research projects, needs some more funding to get things started. On our social media, we have asked you to share our story and cause in order to promote it. You have kept us going, and together we have gone from €30,000 raised as of May 2015, to over €534,000 today. It’s absolutely amazing, and humbling, but this only brings us past the halfway mark.

So far, we have resisted the temptation to ask you to give again, though we know many of you have and we are so grateful for your generosity. Sadly friends, time is running out for Dylan and others suffering from MSD.

And so, we have decided to try to take one giant step in our fundraising campaign in one single day, on 3rd October, for Dylan’s 4th birthday! We are asking all of the people who have so generously helped our family before to give him the gift of life.

We hope to raise as big a part of the remaining €466,000 as possible as his birthday gift, on this one day at SavingDylan.com . You may think it’s very ambitious… but it could very well happen with your help! Your previous support has made us believe and dream of happier birthdays in Dylan’s future.

To reach this goal, on 3rd October, we would need all of our supporters to be as generous as they possibly can. Dare I say, a donation similar to what you previously gave would be wonderful if your means can allow it… This will be our ONLY donation request to you this year, as it must happen now. If you were planning to give again later in the year, please do so on the 3rd October. This request is to you. Dylan’s chance at a real future is one generous birthday gift away from stopping/curing MSD in time for Dylan to benefit. Will you be able to give this birthday gift?

My wife Michelle and I have worn out the word thanks to those that have helped to save our son’s life… Words are never enough, I wish I could measure our gratitude for you to clearly see! I promise you that your money will help to beat MSD. We are doing everything possible for Dylan and as many living patients and those of tomorrow to benefit.

Thank you for reading and for your understanding, writing this and asking outright was difficult for me, I thought long and hard about this. I hope you understand I must try everything that’s possible to save my son’s life as I’m sure you would if you were dealt the hand that my family has been given.


Thank you so much

Alan Finglas (Dylan’s Dad) [email protected]

Please Help make Dylan’s 4th Birthday on Oct 3rd a special one that we will remember forever!

- Please Donate @ www.SavingDylan.com/campaign


Give Dylan’s Birthday Gift at www.SavingDylan.com

or by cheque to: MSD Action Foundation, Grattan Lodge, Balgriffin, Dublin 13.

Cheques must be made out to ‘MSD Action Foundation’ - or - ‘Saving Dylan’

They are one in the same body with a common goal which is ‘To promote and support research that will lead to positive clinical outcomes for patients suffering from Multiple Sulfatase Deficiency’

Our charitable tax exemption no. CHY 21493 - Our registered charity no. 20100957

*Company donation receipts can be issued upon request by email.

Support our dance class and Join us in the Wright Venue tonight for our race night following by dancing the night away in Wrights. Some tickets available at the door. 7.30 start. €10 adult and €5 U18 must be off premises by 10.15 X

Carolan School Race Night- we would love if you can support it

Our Race night takes place in the Purple Room in the Wright Venue on Saturday June 11th. Tickets for the night are €10 and you are in the Wright Venue for the night. We've also decided to do an U18 ticket price of €5 (as they need to be off premises at 10pm)

We would love your support on the night and it will be a great laugh. You can get tickets though any of the dancers and parents from the school of by contacting us here.

Thanks a million
Xx

Carolan School Race Night- we would love if you can support it

Our Race night takes place in the Purple Room in the Wright Venue on Saturday June 11th. Tickets for the night are €10 and you are in the Wright Venue for the night. We've also decided to do an U18 ticket price of €5 (as they need to be off premises at 10pm)

We would love your support on the night and it will be a great laugh. You can get tickets though any of the dancers and parents from the school of by contacting us here.

Thanks a million
Xx

Order going in shortly if anyone would like anything. Sun cream very popular this week!!! 👍🏻

Welcome to all my new likes. Please contact me for any information on our products or feel free to browse my online store

http://yvonnesaloestore.myforever.biz

aloe inspired Helping You to be Healthier Founded in 1978, and operating in over 150 countries, Forever and its affiliates have become the largest grower, manufacturer and distributor of aloe vera and bee products in the world. Avoiding the use of herbicides and pesticides, our patented stabilisation process ensu...