Guestbook

Just read about Molly and her ilness, my heart goes out to her family, i have never cried so much in my life. RIP Molly love you XXXX

Hi guys
Well we have ELECTRIC guitars on the 11th so i will definetly be singing on stage!!!
Yes I called katie at work blubbing like a baby - she did not know what i was saying as i sounded like i was on helium!!
See you there Love
God willing!!!!! no rain or trouble!!!

MXX

hi emma jackson!!!
i hope you will be bringing the guitar on the 11th october...i have mailed katie, my parents and pauline/lucy etc to let them know the new date...im so sorry it was postponed, kate said how gutted you all were...sure this one will be bigger and better...lots of love to you all...cant wait to meet mackenzie!!!! clare, dave & milly xxxx

Hi,
I just read about beautiful Molly Moo through a YouTube video in her honor.
She had such a amazing smile (it made me smile instanly!!!) and a zest for life.
Although I'll never met her, I know she was a cheeky, lovely, beautiful and caring girl.
You guys to do a great job raising awareness. Good luck in the future.
--Ella

Hi Emma,
Not sure if you remember me,It's Lara. I worked at Cannock house and looked after Molly in Tracey's room. I joined the group on Facebook and have been looking through this great website you have created. I think you and your family are doing an amazing job.

Molly really did make an impact to whoever she met,was always a ray of sunshine and will definately be testing the angels patinece with her chatting!! lol! I feel privileged to have known such a special little girl..

Hopefully I will be able to make your 'Dream Rides' day, I wasn't aware of it before so in a way am happy it was postponed so I can come along! Hopefully see you there,

Lots of Love,

Lara xx

I know she will be having so much fun up there xx

God Bless xx

Thank you so much for your support
I cannot begin to say the tears that have been shed due to these 'unforeseen circumstances'.
We will be back and as molly never gave up we will not
We are just so fed up now
life is wrong why do the baddies get the better deal
MXX

I hope its even bigger on the new date, and dont let the scumbags get to you, be strong, and you`ll get it all sorted !

Hi Emma, do not despair at the postponement of Dream Rides. All will be right in the end. These things are sent to try us and in the end will make us stronger

Hi Jo
I hope all is well thank you so much,
Rob has emaied you about meeting up it has been too long! are you any closer to being back at GOSH
I have 1 year to go at college and then apply for the play specialist course need your help ther!!
MXXX

HI Emma and Paul,
congratulations on the arrival of mackenzie,fantastic news,iam sure molly will be watchin over her little bro .
take care
lots of love to megan,
jo(play specialist)xxxx

Hi all, it's Claire one of the ccn team from Bromley, wonderful to hear about your new arrival. I'm not actually working any more as live in Ireland and my third baby had much the same enterance to the world as yours! I think of you all.

She's 5 months now- how time flys! Hope Megan is doing well too xxxxx

Hi All
Yes I had mackenzied at home on 29th July at 9.40am weighing 9lbs!
I had no time to think as labour was 1 1/2 hours so really intense but quick how i like it!!
Very like Molly as a baby he is his daddy though and very good lungs!!
Love to all and thanks for all the cards and pressiesXXXXX
Dream Rides 30th August!!

Nice to hear from you. Have you had your baby now? Look forward to hearing all the news. Love to you and all your family. Take care.
Lynn & Jessica
xx

Hello
First of all thank you Haylee for your lovely message and hope you are well.
Hi Lynn, Thank you so much for donating and love to your family - I hope to be back at classes in afew months as due to give birth to a little boy aaargh!! in four weeks so must get back in shape and just knowing people still think of our molly is all that counts!!
Fran has been great as i have kept her uptodate via email on whats been going on i really miss the classes although the searing cramps the next day are not so missed hahaha!!
just so unfit you must be superwoman by now!
See you soon and thank you so much
Emma XXX

Hi emma,

Not sure if you remember me but my daughter Jessica went to Cannock Nursery with Molly. I am so sorry to hear your news and have never found you or seen you to speak to since that awful time. Jessica always asked how she was and was very sad when I told her Molly had died. I have seen your link through Flins Fitness Newsletter - yes I still go! I remember seeing you there a long time ago. I have just been looking at your website and all the beautiful photos. I also read the article about Molly and Hannah and how they met and became friends. I cannot believe just how strong you have all been as a family, what you've been through and how brave and happy Molly was. A very emotional moving story. Lots of love to you all. Unfortunately we will not be around on the Saturday for the fun day but will be thinking of you and I will donate using the web link. Hope to see you soon.
Lynn & Jessica
x

Hi,

I am so sorry for your loss. May Molly r.i.p - what a beautiful smile she has.
I found details on molly on you tube as I was researching the GOSH, I am hoping to run the London Marathon in April 2009 for the GOSH. I will find out if I have been excepted in October. I will be thinking of Molly- may her spirt live on forever. What a beautiful inspirational young girl. xx

Oh am i really cruel Michelle
But Post master general may be OOOOOOO
HHAHAHAHAHAHAHAHAHAHHA
I love it
MXMXXMXMMXMXMXMXMXMXMX

Sorry for the lack of message board at the mo - a fire has wrecked the American HQ of the company which hosts it. Hopefully it will be up and running again by Monday afternoon. And Michelle's post count will probably be reset to zero! ;)

hi there cannot get into message board
just to say hi all
hope you are all well
i did 6 mile walk today for andy
at least it was dry!!!!
speak soon mxxxx

hi emma,
just realised you asked me to call Rob,i dont have a mobile number for him i will give you my number via robs hotmail.
jo

hi emma,
im fine,decided i want to return to being a play specialist i miss it so much,just waiting for the right opportunity.How is your course going ,when do you start the hps course?just let me know if i can help at all.
take care
lots of love jo x

Hi Jo
How are you
We must catch up we miss you at the hospital God Knows they need you there!!
Call rob on mobile
MXX

just read the article about molly and Hannah,what a fab picture of the girls together.it brought back so many happy memories of my time working at Gosh,i think of you all so much.
lots of love jo (play specialist)

Molly was a very special child - I just read about Molly and Hannah - with tears running down my cheeks - God Bless

I've just read Molly's story on Dailymail and it brought me to tears. How incredibly strong was Molly in fighting her cancer. I'm sure that Molly is having a good time in Heaven and bringing happiness to the others around her like she did for Hannah.

Take care and God Bless =)

Dear Molly's Family

What an inspiration to us all! I found the article on both Hannah and Molly truly amazing - making me cry with both wonder and gratitude for the joy that I have with my daughter Mollie!

Wishing Hannah and all other survivors of this dreadful disease a very healthy and happy life.

Sorry I meant to say before a big big thank you to everyone who read the mail and donated on Moos site thank you all monies are going to a great cause and we will help fund research into wilms and hopefully if not a cure an earlier detection
MXX

Hi Emma

Thank you so much for coming on to our site to leave a message when i am sure old wounds were opened.
I love to hear stories of survial from WILMS as it gives so much hope to parents and childen dealing with this cancer right now!
God bless and stay in touch as you may wish to attend a fund raiser and you would be a key person to be there as you are a true survivor....
All our love
MXXXX

I read recently read the article in the paper and was very moved by it and felt that I had to add a comment on your website. I too had Wilms Tumour in both Kidneys in 1974 and it brought back a lot of memories for me even though I was only 4 years old.

I wish you and your organisation well.

Thank you to everybody who has left lovely messages of support to rob and myself, and to Hannah and her family.
we really appreciate the support and hope that through articles like the mail more awarenesss can be made and of course to show the world how proud we are of our MOO MOO !!!
MXX

I watched your programme when it was aired and read the story in the magazine. My cousin Julie knows your family. I cried buckets. I have five children and 3 Grandchildren and could not imagine losing any of them. Your beautiful Molly, the most cutest, charming and funny little girl, whos dealing with her illness is an inspiration to others. My heart is with you all and good luck with the site and fundraising xxxx

Your story was both heartbreaking and beautiful. Deepest condolences that this tragedy had to visit your family. I am sure Molly will live forever in your hearts and those of everyone that she touched in some way.

I meant to say ' Princess, not Princes' sorry, I have carpal tunnel syndrome and it makes typing difficult sometimes. I do apologise xx

What a beautifull little princes who had a heart of gold and a sea of courage.
I read the story of Molly and Hannah in the Dailymail online tonight and it brought me to tears over and over.
So I did a search on her name and found this website aswell as the your YouTube tribute to Molly entitled - . ' Molly Moo we miss you'
My heart goes out to you Mum and Dad and also to her brother,
I cant function as to what to say except that Molly has brought to light a disease I never knew existed to the under 5's.
Her life and her courage has inspired me to be a better Mum than before, to cherish every moment I have with my daughter even moreso , to check her daily for anything 'wrong' and also, most importantly, to say Thank you to Molly for being the precious little Girl she was to everyone.
Molly will live on in my memory, and from your dedication to bringing this illness to our attention many more lives will be saved I hope.
Forever in your debt dearest Molly.xx

I too just finished reading about your sweet little girl in the Daily Mail. Your sweet angel was a day younger than my daughter Gracie. I just wanted to wish you my best, as I sit here far away in tears still.
God Bless

I have just read your story and send my love to you all- whata wonderful, inspirational little girl. I trained at Great Ormond Street, and am so glad that you found the care there good. It is a wonderful place but made wonderfull by children like Molly and Hannah. All the best xxx

I have just read the story about Mollie and Hannah in the Daily Mail and cried . What a brave little girl. Molly was wise beyond her yearsIt makes a grandmother like me so very sad and very humble

i am twelve and have a cousin mollys age. i cried when i read molly and hannahs story, it is heartbreaking. i hope hannah is ok and still fighting. give her my love
xxx

Hi

I've just read the Daily Mail's article and it brought tears to my eyes too!!

What a special little girl.

I just wanted to wish you and your organisation well.

I have just read your story about Mollie & Hannah in the Daily Mail & it has left me in tears.

What a brave & inspirational little girl your Mollie was, who even through her sickness gave Hannah the push to accept her treatment. You must be so proud of her as she has touched so many peoples hearts as they hear about her, like it did mine when I read the article.

I'm so sorry to hear you lost Mollie, but I believe that heaven has gained a very special little girl whom I am sure will still be helping others.

God bless you all & good luck with your campaign. I also wish you well with your course & hope you fulfil your dream about working at Great Ormond Street.

Sue

Hey Michelle from Cork
Where are you
How was new York???
Let me Know
MXX

Hello I didn't know Molly but I know your family a little bit I just wanted to say godbless take care xxxxx

Hi Karen
I have left you a personal message on Jessicas page.
pray you are coping as well as you can
please contact me when youare ready as i have some things to privatelydiscuss regarding wilms.
love as always
X

Please contact us at the wilms web address given on the contact and enquiries site it may seem like a lot of info needed but once registered I can respond personally to anyone who wishes to talk about Wilms or anything really
If you have registered to the forum you can log on to my personal email which i do reply to (yes i do all you non believers) I really would like to speak to parents with wilms children and of course parents like ourselves that have lost children as we are arranging a major charity event to take place in summer 2008 for WILMS.
We cannot eradicate WILMS overnight but awareness is knowledge and there are so many people like Lin and Mike Barringer who lost their beautiful daughter sophie and karen who lost Jessica who can make such a difference - lets do it no more 'What is WILMS' more of 'Lets beat WILMS'

Dear Karen
I do not know how to express my sorrow for you to lose jessica, and the fact you are thinking of us when all you were dealing with and now sadly living with the loss that so many parents cannot comprehend.
Even as a mother so similar to yourself, I still cannot understand your pain as are children are our worlds, You are an amazing mum and jessica (like Molly) knows what we feel and how much we cannot change the situation wish it was us and not them.
I would say time will make things more bearable - but sorry it doesnt - you never get over a loss this painful but you do learn to deal with it slightly better day by day.
I get through by knowing no more pain to molly or jessica and they like all the children have christmas and Disney everyday. Sending you and your strong family love
and in the future we pray to God will meet as we are planning a massive Walk the world for Wilms donations hitting £20,000 projected lets do this for Jessica , Molly Sophie Barringer, and Rosie Pepper and all the children
XXXXXX

Hi, I watched your little Molly on 'Child In A Million' in Feb and cried throughout the entire programme. I could not help but think how brave a family you were, yet now you should be proud for what you are continuing do in memoy of your precious daughter. I was probably more upset because Molly's story was similar to that of ours. My daughter Jessica had been fighting stage four Wilms for a year when Molly's story was aired on TV. It hit home how serious the illness was. In March a month after watching Molly, we were told that Jessica could not be cured, but because her Wilms was so unusual they could not give us a time. Me and my husband found the strength somewhere, to make Jessica's time special. Trips to Disney, holidays etc. Sadly Jessica died Nov 26th 2007, just before Christmas. I would just like to say how sorry I am for your loss. The work you are doing to help fight this disease is wonderful. All the best Karen x

Hi, I just had to write in. Although I didn't know Molly and I do not know her family. I have thought about you every day since watching 'Child in a Million.' Especially on Mollys birthday, Christmas Day and the first anniversary. I really hope you are all ok. When I think how sad it makes me feel and knowing it is absolutley nothing in comparison to how Mollys mum and dad feel. I hope you are ok and I wish there was something that could be said to take the pain and heartache away. I have never wanted to hug 2 complete strangers as much as I want to hug you two!! Molly could not have wished for two more loving parents as you two. You have done so well to turn a tragedy into something so positive. xxxx

Hi Anna,

I've not seen the pictures - I will post them in the gallery if you email some to me at wilmsinfo@btinternet.com

Cheers
Keith

i just wondered if you recived the photoes of my house at christmas it was in memmory of molly . lisa champ has vidioe of house and the ballons we sent to molly god bless anna

i just wondered if you recived the photoes of my house at christmas it was in memmory of molly . lisa champ has vidioe of house and the ballons we sent to molly god bless anna

i just wondered if you recived the photoes of my house at christmas it was in memmory of molly . lisa champ has vidioe of house and the ballons we sent to molly god bless anna

i just wondered if you recived the photoes of my house at christmas it was in memmory of molly . lisa champ has vidioe of house and the ballons we sent to molly god bless anna

i just wondered if you recived the photoes of my house at christmas it was in memmory of molly . lisa champ has vidioe of house and the ballons we sent to molly god bless anna

Glad tidings etc! Hope everyone has an absolute doozie of a Christmas!

Hi Emma Rob and little Megan, i hope you are all keeping well. I now have a little boy Euan who is keeping me very busy. He's finally asleep so i thought i'd log on and check out your website, which is fab by the way. Molly would be so proud. I think about her all the time and especially of you guys at the moment. Christmas will be tough for you but just imagine molly dancing around with pink santas where she is. It would be lovely to catch up with you all soon for a cuppa. Lots of love and hugs Ceara, Mollys community nurse and biggest fan. p.s. say hello to that mad Irish mother of yours Emma xxxx

Happy Birthday Molly. Sorry its late. Luv to you all.

i did not know molly only throug afriend this year all my christmas lights are dedicated to a buetyful angel and all the angels that people have lost god bless you all
anna byrne penge

Hi To everybody, Claire thank you so much lovely to see you meet soon or else!!! Fi and Mox so sorry it has been so long please call we will hunt you both down!!
Through a stream of tears thank you for all yout birthday monies for moo and thank you all just for remembering her bday it means so much. We have pics on gallery showing all the balloons around the world going of!
You are all amazing!!!
Special kisses to Andy and Michelle praying for you..
MXXX

hello, hope you are all well, just wanted to let you know i am thinking of molly on her special day, as im sure many are!! i bet she is having a great pink and girly party with all the angels!! take care, hope to see you soon! xx

Happy 6th Birthday Molly.XXX

Oh yes Michelle Shout going out my till is the best thing that the early learning centre ever invented. Coffee spill aisle 2!!!
Sorry i have not been on site for a while will catch up now College is manic and not happy at all about it and want to quit now tell you more privately, stress at time of moos bday is taking it out of me and i cannot cope with it sometimes and feel i am wasting my time.
Positive vibe I filled in a form at college course and have moved to new age bracket - i now tick box 31-40 WOOWOO god i feel old
MXXXXXX
MXXXXXXXX

emma when you put your call out on glynis were you using your till thing you showed me the other day knowing how attached you were to that..
hope megans birthday went ok for you all...mx

Glynis call out for Glynis
you left a message regarding your god daughter forgive me if i have this wrong. you were searching sites on WILMS forgive me for not answering it was a drastic oversight that i apologise for please let me know if Shannon is ok
MXX once again apologies if names are incorrect!!

Hi Michelle give your mam big kisses from us all
New York New York have you been there b4 I am lucky enough to have gone twice and it is still not enough!
check out the grenwich village area for bars and remember do not let cabs rip you off on the way back to airport PREBOOK from hotel or else you could get done for $1OO we booked and average to JFK is $50 so do it!!
fingers xd and toes for checks on your kidney love it baby you only have one - no what I mean!! look after it...
MXXXX Megan 1 on Tuesday 30th October oh my god!

was reading sum of d comments 2u..ppl r u nice..wish u all d luck wit ur college course..my mam says hello n says molly is beautiful i was showin her dis web page...im off 2new york on d 16th of nov i cant wait 4time away from work..im 19 a week later n also wit my bf 3years..i hav 2go 4my check up in d next couple of months just 2c how my kidney is doing..plz stay in touch n ill ay a prayer for molly on her bday xxxxxxxxxxx

Hi Michelle How are you doing my love
As you can see Child in a million was aired in Australia and the fantastic response from everybody has been such a comfort to us all - once again THANK YOU ALL!!
I hope your well and no problems, i am enjoying college and am working as a placement at molly's nursery she went to for 4 years nearly it is hard and emotional but i need to be close to Molly - all the staff at the nursery remember my moo and of course her mad mother!!
Great Ormond Street here I come
Rob and I will be going there as we do frequently but we want to go there Christmas morning to give out our treasure bags to the children who cannot get out for Xmas.
I also want to go there to be close to moo and her birthday is 12th november so we will be releasing 6 pink balloons into the sky on that day - many people including my sister are arranging this in different parts of the UK and maybe worldwide if anyone does do it please take pictures and send them to our webpage so we can upload them in our gallery here - please note I am not asking everyone to do this only if they had planned it.
Just knowing people think of my moo is the reason we are here. Megan is 1 on the 30th October aaarggh!!!
Love to you alland soon designed by my buddie marina we have a xmas newsletter coming out to update people on funds and thank yous!!
MXXXXX

hey emma michelle ere from cork hows things going 4u...i still cum on dis site all d time it just makes me appracite things a lil more...i think of molly all d time.. take care chat soon xxxxxxxx

After watching that tv serie i felt so sad for molly "Poor Thing" that really upset me to it even made me cry. Hope every thing goes well with the new baby
Lots of love and wishes emily

I'm another Australia (from Brisbane!) who saw Molly on Child in a Million this week. Watching away, I was so excited when her treatment appeared to be going so well and she didn't need the second operation. And then the narrator said her tumour recurred and she passed away. I sat there looking at the TV and just said 'NO!'. The world is a sadder place without your amazing little star. God Bless you all.

The end of the show was like being hit by a ton of bricks...I was so upset after hearing that Molly didnt make it after all of that positive news regarding the cancer. I couldnt stop thinking about Molly that night and the next day at work. She was very brave and took each challenge head on with smiles and laughter. Her face will be etched in my mind for many years if not the rest of my life. My wife and I cried openly after the show. I hope your second child brings you so much happyness and believe me I hug my kids that much tighter now. They are so precious and I hope I never have to go through what you guys have. Keep the spirit of Molly alive. She was 1 in a million for sure....xx

Watched the program 2 nights ago, the outcome saddened us so much we have been deeply moved for the past 2 days. I am terribly sorry about the outcome, It was unexpected. Our thoughts go out to you all. Molly was such a happy and bubbly child, a true inspiration for strength. I'm sorry. Kindest regards from Australia.

Wow is all I can say, Molly was such a bright spirited little girl who touched everyone around her & will continue to do this, my heart goes out to you & your family, always thinking of you & all the best for your future. for you Molly :-) xoxoxo

To say how deeply touched and moved I was by Molly and yourselves is an uderstatement. That beautiful, loving, courageous, sparkling little girl with such amazing insight has touched the lives of so many and is an inspiration to us all. She was an absolute delight. Thank you for sharing Molly's story. My very best wishes to your family.

Thankyou for sharing your story with the world. What a little character Molly was. She made me laugh and she made me cry. I wish you and your family all the best for the future.

Emma and Rob - what an amazing little girl Molly was - so bright and full of personality and gorgeously cheeky in all the right ways. She was such a strong little girl - you must be so incredibly proud of your little Moo. My heart goes out to you - Molly has touched many hearts and we are all wiser for seeing One in a Million.

I too watched child in a million last night:

All I can say is what an amazing little angle!

I watched Child in a Million last night. I have to say I really wasn't expecting the end of the show, I just sat on the couch bawling my eyes out. I then went into my 13 month olds room and picked him up (while he was sleeping mind you) just to smell him and hold him. I was so touched by beautiful Mollys bright smile and courage. To Emma, Rob and Megan - God Bless you and your strength. We take so many things for granted but from now on I'm going to cherish every minute with my son. Thank you for sharing your story. Love Tina and family

WOW G'day guys and gals WOW a big big thankyou from Rob and myself for your beautiful messages, we did not know that Child in a million was on air in oz.
Blimey strewth!!!
We are keeping busy (or should I say Molly is keeping us busy!!)
I am back in full time college to do a childcare diploma and fingers xd work at Great ormand Street as a child play specialist.
Rob is still here HAHAHA!!
We cannot believe Megan will be 1 in 2 weeks time it has gone so fast but yet so slow without our precious molly moo moo.
My uncle lives in Brisbane and he has just recently flown home from being here for nearly 6 weeks.
Thank you for your support once again and check out the forum and pictures of Moo in the gallery
Plenty of Molly on Youtube just type in her name

Love to you all (throw a shrimp on the barby for me) I know i am not funny!
Love Emma Rob and Megan never forgetting Moo Moo.........

My family and i were just flicking through the channels here in Australia when Molly's story caught our attention and hearts.

Our thoughts go out to Molly's family and hope they know that their beautiful daughter's story has touched Australia as well as the UK.

Gorgeous little Molly, an inspiration to us all. I really thought the ending was going to be a happy one for this beautiful little girl. I feel so sad for Molly and her lovely family, i cant imagine what this would be like to actually go through something like this with your child. Being a nurse i am constantly amazed by kids and how they handle things and Molly was no exception, showing us just what a brave little trooper she was. God bless her and her famliy x

It's almost a couple of hours now since the story of Molly was aired and I am still wiping away the tears. I was deeply, deeply saddened at the outcome. My heart goes out to you. I cannot imagine what it would be like to go through anything like that for all of you. Molly was put on this Earth to touch so many people...her courage and strength throughout the ordeal will always remain with me and of course who could ever forget that beautiful smile. I bet she was the proudest big sister ever.

Hi, I have just finished watching Molly's story which has just aired in Australia. I was deeply saddened by the outcome of little Molly's story. What a beautiful little girl who I am sure is watching over her loved ones.

Hi, i just finished watching the show aired about half an hour ago here in Australia. I have been deeply touched by Molly's story. what an amazing young child. The natural level of maturity that far exceeded her age. From what i saw on the show Molly seemed ecstatic to go to school. I myself have been through an experience similar to Molly and her families. My sister had a heart problem and then was operated and unfortunately she passed away. one year after my mother miscarried. 6 months later my mother was pregnant with me. I am now 16 years old and very happy. Just letting Molly's parents and sister know that things do get better.sometimes it becomes unbearable. The pain never goes away but this experience will make you far far stronger and know whats important to you. I have always felt guilt that i was the one that survived and not my sister. but thats just the way that things happen. Good luck with your family's purstuits.

Hi I live in Australia and I have just finished watching the story on television about your precious little girl Molly. Iam so deeply sorry for your loss I cant even begin to imagine the hurt you must be going through. She was an absolute breath of fresh air and you both should be so so proud of the beautiful young lady you raised. She really was an old soul. She will always remain in my heart and you and your family will be in my prayers. Stay strong xxx

i watched a show on t.v here in Australia which showed the story of your gorgeous daughter Mollie,as i watched it i of course was unaware of the outcome for mollie, as soon as i saw her and listened to her i got a feeling that she was a very "old soul" very bright and of course very special. I was so very sad when i realised that she had not beaten this terrible disease. i watched this show for 30 minutes and felt such sadness, I hope you are both doing ok and wish your family all the very best

I saw Molly's story on tv tonight here in Australia. I lost my cousin when we were little to cancer and Molly reminded me of her. I miss her and her beautiful little soul. Molly surely is a beautiful little angel up in heaven.
Glod bless

We live in Australia and have just seen the documentary on TV regarding your little girl Molly. Our hearts broke with the outcome and we are deeply saddened and sorry for your loss. Molly has touched our hearts, she has the most beautiful smile and fun loving, outgoing attitude. She was so grown up. Your family will always be in our thoughts and we wish you the best for the future ... and we do think Molly will be watching over her little sister. xx

Having just watched the story of Molly, i'm still wiping the tears from my eyes. What a brave family and a wonderful little girl. May she be in a very special place.

I was reminded on soo many levels of a similar fight our family had late last year. My daughter is the same age as Molly, and managed to overcome a Ependymoma brain tumor after a large 7 hour operation and follow up Radiotherapy. Seeing the parents of Molly watching thier daughter go into surgery, and undergo treatment brough back some very painful memories.

Brave family and a wonderful little girl who is no doubt looking down on us all with her fairy wings.

Saw the show in Australia and was very touched by Molly and what she went through. I cant imagine how the parents coped or are coping now... I could see Molly in my own child Rohan...(3 now)...He as molly did has so much life to live for and yet for Molly this was unfairly taken away. Very Very Sad.......

Dear Rob & Emma
Child in a Million just aired here in Australia. It was such a rollercoaster watching Molly's story just over half an hour; I can't imagine what it was like to live through it. The tears are still rolling. How blessed you were to have such a special little girl. All the best with your baby Megan and for the rest of your family for the future. Thank you for sharing your story.
Love Cassie

WwW.SparkleTags.Com

sorry guys left a really nice message and this arse guestbook did not print it so again thank you kevin for your kind donation love to family and send kisses to amanda ellie and alana, sorry karen please call rob and maria it is a privelage to see your son ( names protected for childcare reasons please understand) he is a delight to look after thank you so much for all your messages moo is lookin after all your children and making sure they are all ok that is her purpose and that is why we had to let go...........................................

Dear Emma and Rob, everytime I have attempted to contact you I didn't know what to say. I just hope life will get easier for you and your new baby. Love Maria, Takeshi, little Maria and Alex (Cannock).

Hi Rob & Emma. It has taken me this long to try and think of the right thing to say. I really don't know what to say apart from how sorry I am about Molly. I think this site is great and I keep looking on here with my girls and looking at all the pictures of Molly. Kirsty ran race for life in memory of Molly in July and she completed the race in 27 minutes, she also raised £75. Molly certainly was a happy and pretty little girl even though she was going through such a rough time. Take care. Love Karen and family. xxxx

Hi Emma&Rob,
Have tried for a while to track you down&finally come across this site!When i heard about Molly I was extremely upset.Ive made a small donation on behalf of Alana&Ellie.Wish you both the very best for the future!
Kev,alana&ellie

Hello, I thought I would drop by the site as I was thinking about you all, I saw my last message and realised the spell check had gone crazy and put the word "dissapeared" in, sorry about that.

Take care, Viks

Hi Emma, my msg didnt go through the other day, sorry!! Hope your ok and hope your loving us college girls as much as we love you!?! Im always here for you and so r the other girlys!!! Ur baby was such a cutie and i know your gonna pass this course for her!!! Lts of love hugs and kissess xxxxxx katie xxxxxx ps: party it up on my 18th xxxxxx

Hi,

Emma, so glad that college is going well, Rob had better watch out you might pull yourself a toyboy!

Still cant get on to the wilms forum, so hi to Michelle Aunty Karen and everyone else! XXXXXXXXXXXXXXX

Once more thank you all so much for your donations on just giving thank you!!!!
davey and angela well done and see you on Jens great north run for moo!!! angie drink lots of water and davey be prepared to look after the kids HAHAHA!
Michelle well done and thank you lets get this forum back on sorry you are always on your noddy but we try to get on but college and work interfere
thank you for your dedication as sarah
and any one new dont be afraid get on it!!

emma
15 years not a problem!!!!

there are 11 years between andy and i
youd never know
hes so immature....
bless him....
mx

Sarah not sure will try later to log on a job for my bro i think As you can see everyone at college is fab and i dont think a 15 year age gap is alot ...................................MXX

Hi Bromley crew!!! I am so hip (not)
You made me cry!!
Thank you so much lets pass this course or else maggie will get you!!
MXXXXXXX

Hello all, I cant log onto the wilms message forum anymore, is anyone else noticing this? Xxxxxxxx

emma, when i first saw you at college i thought blimey! she's old!! no im joking! you're already a legend and the girls at college LOVE you, after looking at your website i would just like to say you are an inspiration and i admire you for being so strong, this website is amazing, well done keep strong!!!

EMMA hello my love. when i first saw u i was scared i did'nt no OLD (only joking ur gorg) people would be in our calss, but your such a lovely berping buddie, i hope you like your course.
YOUR just AMAZING!! mwah
love you lots xxxxxxxxxxxxxxxxx

hey emma its yaz from college wooo!.. your little girl is so beautiful and u should be so proud ! : )...just want you to no that we are all here for you.. stay strong love yaz xxxxxx

Hi guys
Michelle in Ireland my own mother is a born and bred irish women she is from dungarvan and we have a cottage just outside there and we visit when we can we are trying to get there in spring 2008 as i am comitted to a course in childcare now so please keep in touch as we would love to meet you in ireland wherever you may be cork or dublin
i have amultitude of family in ireland what a knees up you could take me an old fart and my irish cousins to a good hotspot
your bravery as your family is astounding plus we are organising a big event "walk for Wilms" why not start one in Ireland MX
MXX

Thanks sheila lets be honest the sausages were pretty rank HAHA just joking. I am now in the cool gang and accepted i hope rock on exams bring it on!!
I still cannot grasp teenage talk they think i am some sort of crude woman or damn right deranged!
welcome to the world of Emma
thank you all stay in touch all of you try the forum if not your thing stay here!!!

Hi emma & rob

Just seen the beautiful photo's of Molly on youtube, still can't believe she's not here anymore. Jasmine had put the photo of her and Molly in her special box but took it out last week and placed it on her bookshelf, I know she still misses Molly as we all do. I thought of you all at the weekend when it was only a year ago we were all sitting round the table eating dinner, the night before em's birthday (I was so pleased she ate my chicken that day, not like the sausages that made her feel sick!).

Anyway, we are always here for you and know em that you will do amazingly in this course. We will never forget Molly, she will always have a special place in our hearts.

love

Sheila, Kevin and Jasmine xx

hi michelle
can read that better
you sound like a very strong young lady
i guess you get that from your mum wth all she went through with yourself......
unfortunately cancer affects many families it is dreadful

you take care
best wishes mx

sorry about my short txting i hope this is a bit better well molly touched every body like my mother went through d same thing as emma but luckily enough im still here my aunt also died of cancer n my uncle so i no how it feels 2lose someone 2this horrible disease

hi michelle
well like emma said so pleased to hear good stories
we need more of them

show my age now found your text well hard to read bless you.....i still type full length words on here and texting!!!

can we get translator on here!!!!

anyway glad to see someone else on here and aware....

SPREAD THE WORD!!!!!

hi i wld lv 2help wit ne thing but i live in cork dats in ireland i wld like if u also kept in contact wit me my mother also wishes ye d best of luck n says ye r very brave... wen i had my chemo n my kidney removed i had 2go 2dublin becuz they didnt hav d equiment 2deal wit it in cork my doctors were fab n they were d best 2me im was lucky dat my hair didnt fall out it just got very tin on 1side n it is still very tin on d 1side till dis day... my tumour weighed 1kg but its mollys story dat is after touching me

Hi Michelle
Thank you so much for logging on today. Thats what we want to hear Wilms Survivours Good luck with everything and stay in touch cos you might want to come to some fundraisers you would be an inspiration to a lot of kids with Wilms. Love to your mum as well she deserves it as you do!

hi well i read ur story on take a break n it got me thinkin wen i was 1n 3months i was also diagnosed wit a wilms tumour also but i was lucky i survived but it took a while 2be spotted if my mother didnt keep bringing me 2d docs i wldnt be ere 2day for 17years of my life i had 2get check ups n i hav so many scars from ops n over tubes but im grateful im 18 now n in about 5years ill hav 2get a check on my surving kidney 2c how it is gettin on i hope 2of ye n megan luck in d future xxxxx

Hi Sam, Viks, Emma and Denise
Thank you so much for your messages of kindness and support. Viks we will contact you about your fantastic postpals site my god kids need you!! What an amazing thing you do!
To all of you who take time out to check out our site for Molly we really appreciate it, please fell free to log into the forum I understand it can get so many topics but all fun and poor Michelle needs company!! hahah
I am about to leave my job of 10 years to start a childcare diploma at college for 2 years on the 10th sept (my 31st birthday) AAAAGHHHHHH!
i am so scared but to achieve my goal of child play specialist at Great ormond street i will do it!!
thank you all as i say all the time we cannot do it without you all !
God bless
MXXX

i would just like to say that i have just read Molly's strory in take a break and i broke my heart. what a courageous little girl who was not frightened at all. she is an inspiration and wasnt afraid of anything. she was glad she left her sister Megan to look after her mum and dad. my heart felt wishes to her parents. I will always think of Molly

i would just like to say that i have just read Molly's strory in take a break and i broke my heart. what a courageous little girl who was not frightened at all. she is an inspiration and wasnt afraid of anything. she was glad she left her sister Megan to look after her mum and dad. my heart felt wishes to her parents. I will always think of Molly

Hello, I saw Molly on Child in a Million, she was so cute, I remember in particular her picking up the telelphone in the room and pretending to chat away on it. I was so sorry to hear at the end of the program that Molly had dissapeared, I did a google search at the time and didn't find this site but after seeing you were in Take a Break this week I thought I would google again.

I was in Take a Break last week reguarding www.postpals.co.uk an organisation brightening the lives of seriously ill children by sending them post. If we can be of help in any way to "We can beat Wilms" or to any families you know then just drop us a line on viks@postpals.co.uk (there is more info about what we do here http://news.bbc.co.uk/1/hi/england/southern_counties/3673782.stm

Best Wishes

Viks

"Its not how long a star shines, what is remembered is the brightness of the light"

www.postpals.co.uk

Hello
My son went to Nursery with Molly and spoke about her constantly. When I met her I knew why. She had the most infectious smile and personality - the most incredible little character. When I heard that she was so ill I was stunned. Who wouldn't be? How could life be that cruel. Then to hear that she had passed away after such a brave fight was crushing. I saw her on Child In A Million and cried my heart out for Rob and Emma. Molly was a credit to them and so so brave in spite of everything she was going through. Rob and Emma - you must have been desperately proud of Molly and now you should be proud of what you are achieving with this website and the fundraising that you are doing. You are incredible people. x

I didnt get to see Molly on TV when it was on but I did read about her story in a magazine on my break at work last night. I really dont know what to say, what an incredible (and beautiful) young lady she was - you must all be so proud of her. Needless to say reading through your story had me in tears and it had the same effect on the others who read it. You are an amazing family and well done for all your support and hard work you provide about wilms tumour.

You are in my thoughts,
love and best wishes,
Emma

I didnt get to see Molly on TV when it was on but I did read about her story in a magazine on my break at work last night. I really dont know what to say, what an incredible (and beautiful) young lady she was - you must all be so proud of her. Needless to say reading through your story had me in tears and it had the same effect on the others who read it. You are an amazing family and well done for all your support and hard work you provide about wilms tumour.

You are in my thoughts,
love and best wishes,
Emma

looking forward to you comeing up to rothbury.see you then.


GEORGE

Hi, I just wanted to let you know how inspirational you and your family are.
I know your sister Karen a little, our youngest children(Poppy and Max),, were born the same week. I think your site is brilliant, its definitely going to raise lots of awareness for a special cause.
I saw the address in our local newspaper and thought I'd have a look! Keep up the good work and take care!
Helen xx

DOH!!!!!!!!!!!!!!!
I meant to say before we cannot continue without all your support DAMN false nails cannot do anything they are so coming off!!!!

Words cannot express our heartfelt thanks everytime we see the donate page. To all of you who did not even know moo but have raised monies through work events or running cancer races we thank you!!!!!
To people who have given a donation that they would of normally spent on their own children and lives every penny counts. We simply could continue without your support and we will continue to arrange fun days so people can all get something back as well as donating money. The Ferrari day was an amazing time and was so well supported THANK YOU ALL YOU ARE THE STARS !!

Hi Emma
Spoke to your mum please call or email rob to catch up so sorry as you will know from your mum been caught up in crap as usual!! thank you love
to everyone who is supporting Wilms and running or walking we are truly grateful as well as people who are just generally raising monies and awareness Rob and I are truly grateful..........................
We cannot keep going without support and this webpage is not just about moos memory it is for future progress in research into Wilms and maybe one day we can say "you know what this is the cause lets treat it" that day will not be soon enough for us but i will continue on and pass it too megan to continue on in her sisters name we will still have a Doctor Biederman who will fight to eradicate child cancer
MX

Hi Emma,

Did you receive my email that I you sent about a week ago? x

Thank you Coral, We are so grateful for everybody's support before and on the day (weather as well never got anyone down!). We cannot do these events without friends family and people who want to help.
Please see forum and gallery for pics of day
We will formally announce results of monies raised on the day. Once again thank you all so much!!!!
Plus Kids from GOSH came down even in the rain and had sponsored rides so they were happy I Hope!!

hope the ferrari day went well.I give my love

George

I do not know mollys family but I went to the farrari day today and i think it is fantastic the way people give up their day and bring their cars along 2 drive people around 4 charity i had so much fun in the ferrari 355 thank you for today and molly was a beautiful girl, so brave and in all the pictures i have seen she was smiling mollys mum and dad have been really strong and are great people doing this stuff for charity. god bless x

your welcome jenny
mum just watching molly with me
she is in love already with her first glimpse..

Hi Michele,

Thankyou ever so much for sponsership I really appreciate it and so does Molly, she is going to be on my left shoulder all the way round.

Jenny.x

got it!!!

Micheele
go to just giving main page go to sponsor a friend then put in jenny egan make sure you leave a gap between names
this should work
bless you

still cannot get it to work....they have to be so precise...i had same probs with mine when i set it up...

WRONG I Got it wrong

www.justgiving.com/jennyegan

Sorry

the full webpage address for Jenny is www.justgiving/jennyegan
many thanks Guys

what is the full link for jenny's site
they are near impossible to find without the full link....
will keith put it in the calendar too??
hope you are all well...mx

Hi guys
just to let you know Jenny moos godmother (the mad woman who flew to Canada the minute she heard about moo). she has a page on justgiving/jennyegan as she is running the great north run for moo.
Moo is running with her.
so any sponsors gladly welcome
thank you

Don't run near me in your condition!!! Congratulations. Yes that is an amazing coincidence, 29th Dec....Molly has definitely got something to do with it!! I have been looking at your other messgaes - you can keep the Jesus Christ superstar video - looks like you'll need it to practice! I am just so chuffed someone else liked it - although your sister is right - you are all mad as snakes! Just one more point re your criticism of Krens dress sense - the Rothbury clothes- we all thik she is the trendiest here, being from the big city and all! See you on the 15th, and take care of yourself and babe. Love to you both, Aileen x

Hi Aileen everyone
well i am ashamed ashamed ashamed i have not run at all but Jenny will beat me up now and I must train we are going to start this week and i am very early pregnant again! YES iam so fingers xd all ok 12 weeks soon!
Due date december 29th 2007!!! Moo has a lot to answer too!
How are you all up there in the hebrides!! whats the stroy with the wigs tshirts sorted here !!
MX

Hello Rob and Emma. Just an update from Rothbury that we are training hard for the race for life in Molly's memory in July. We took to heart your instruction that we HAVE TO RUN and have been inspired to go for it. My husband even bought me new trainers so not all bad (and I think my bum is a bit smaller). Are you still planning to come to run? Hope so and well done with all the fundraising so far, it's amazing. All the best, Aileen

Dear Barb
Thank you so much for your dedication and time to think of us when you and your family have truly been through it.
Please know we and molly included will be thinking and wishing you well not just in your walk for Molly but in all your fantastic fundraising.
This is fabulous we are now INTERNATIONAL GUYS
WE CAN BEAT WILMS IS GOING WORLDWIDE!
Say a big hi to my mad aunt and Bernie too!
love to all family and new friends in Vancouver and the big BC.

Emma and Rob
XXX

My heart goes out to you. Let's hope that we can irradicate all cancers and make this a world full of wonder and not worry.
My family has also been devistated by cancer. My sister Brenda is fighting terminal lung cancer at this time and is a 13 year survivor of colon cancer. I also lost my sister Beryl to breast cancer 13 years ago and I was just getting over my treatments for breast cancer which returned 3 years later. My mom, who will be 91 this year is a 23 year survivor of breast cancer and my brother has just undergone surgery for prostate cancer. Because of this I do the Weekend to End Breast Cancer Walks, here in Vancouver and last year I also walked in the Weekend to Breakthrough Breast Cancer Walk in London, England. My team has so far raised over $50,000.00 to help put an end to cancer.
I work with Bernadette Kelleher, here in Princeton and I told her that this years walk will be in Molly's Memory. She will be with us as we walk the 60 k through the streets of Vancouver and I will be passing on your information about Wilms. Please know my thoughts and prayers are with you.
Sincerely, Barb Gagnon and the Breast Friends Team from British Columbia, Canada

Hi Emma,How are you? Im ok thanks hun. When i left cannock i did end up going back into childcare even though i needed a break from it but did enjoy my time at another nursery..This is all ive done since leaving school so im finding it very hard knowing what else i could do with my working life. Im currently unemployed and looking for work so not sure what i will be doing next.. Would be great to catch up with u properly and have the pleasure in meeting Megan. Hope you are all well speak soon steph Xx

Hi Steph
Thank you my love How are you!! We miss you where are you at now still working at nurseries or elsewhere!
Keep in contact lots to catch up
MX

Hi Emma, Rob. I saw child in a million and was so shocked when i heard of molly having being one of the few who get it...It was heartbreaking.... I knew molly and what a pleasure it was to have known such a speacial little girl... She always put a smile on your face and i'll always have that special place for her in my heart for her... Throughout the years i watched her grow from a young baby to a beautiful little girl. My condolences go out to you... The photos on my tube are lovely i had to look twice due to not seeing them through tears, but it also made me smile. Great site, well done... With love, Steph xxx

Hi Emma and Rob, Just want you to know we are thinking of you. Alex put on his red pjs the other night and said they were the best present he ever had because they help him remember Molly. They are bit short but they will not be parted with and like Molly never forgotten. speak soon love Amanda Alex and all xx

Thank you all for your comments and wishes.
This website is not just about Molly it is about anyone who needs support and a friendly link to help with day to day crap!!!
To all who have illnesses and puppy training (SAM) we are thinking of you and please use US we may not reply straight away i do watch TV alot sorry to say wish i could say i was helping greenpeace or attending mass but really i'm drinking sheds loads of wine and ordering curry what a girl !!! seriously please log to the forum and start a thread which means you can get people to log back and chat it could be about Cancer, other illnesses or even who should win the apprentice we do not care either way we are here GOD BLESS ONE AND ALL!!

What a brilliant and up-lifting web-site, which I would guess also sums up Molly, although I never met her. Heard a lot about her through connection with Emma's employment and viewed the Channel 5 programme with lots of tears. We will make more contributions to future fund-raising. Keep up this vital work.

Hello,
Just been up most of night hunting for info on wilms. It looks as though my goddaughter Shannon has this condition, we will know on Monday.The tumour has burst, and we are waiting for all the test results. Molly is a beautiful child. Please send your prayers. Thank you

A quiet Friday, means i get to daydream about Moo Moo. so thought i'd just have a quick read of some of the messages. It's so lovely that people, no matter what they are going through - personally i'm puppy training and I'm finding that hard - but its really a walk in the park when you read about others, and that they still find time to pass on their support and love. I'd just like to say that Em and Rob are two of the most supportive, loving people, even when Molly was ill they were the most supportive people to everyone else and still managed to smile, its nice to know that this website gives back some of the love and support to them that they truly deserve. Best of luck to the mums and dads out there and their little children who are ill. My prayers are with you all. Big kisses and hugs Moo xxxx

Hi Emma,
It is hopefully pneumonia Milly has not, lung cancer. The docs are not 100% certain. But all the signs are more towards pneumonia then anything else. I have just looked at your pics on 'You tube' and would just like to say again what a lovely little girl Molly was and although it made us cry we couldn't help but smile especially at the one with her laughing with her dinner hanging out of her mouth. Thats Kids! Love Jo x

forgive me for spelling Milly wrong i am also stupid my family will tell you all that

Hi Jo
Thank you so much for coming onto the guestbook at what must be such a difficult time we pray thay Milly is well and her cancer will leave her alone so much pain for such a short life we do understand but i do believe we cannot say we know how you feel because everyone is different but this website is to let everyone know we can do something even if it it is to show that knowledge is the only way i pray for Millie and Molly will send special kisses xxxxx

Although I have never even met Molly and her family, I have thought about them every day since watching 'Child in a Million.' Molly was a beautiful little girl and my heart goes out to her family. My niece Milly who is four has just got over cancer (not Wilms.) But she has developed a cough which is not shifting and we are waiting to find out if the cancer has returned to her lungs. Organisations such as these are brilliant. I really wish you well with it. It's knowing that you are not the only ones going through the awful journey this disease brings.

Hi There,

This is Emma's friend Jenny, I've just told emma about your comment and she wishes you had left some clue to who you are, like you said awareness has to be made about this disease and she would have liked a chance to talk to you especially as a wilm's parent. Hope you don't mind but perhaps you could go into the Forum message board and have a chat with Em on there. Thankyou.xx

hi just wanted to say i think molly was an amazing and brave little girl, my little boy finished treatment for stage3 wilms in nov 06 we saw molly once or twice on elephant daycare she was always smiling. just watched youtube video it is lovely but so sad! i think this site is brilliant and what your doing to raise awareness of wilms is great-XX

Thank you guys for all your messages we read them all the time!
Join the forum it is a laugh but also discusses real life issues and problems

MXXX

Emma & Rob big big smiles to you both (you know what I mean), thank you for the card it means a lot. Miss you and love you lots. XXX

Hi Rob Emma thinking of you both love frank

Hi Rob Emma thinking of you both love frank

Thank you all for supporting me in running the London Marathon. Every penny counts and is invested into the research of this horrible disease, thank you! Molly has touched so many of us, and her strength has been so inspiring. Together we can make a difference!

i love you so much and miss you lots molly. xxxxxxxxxxxxxxxxxxxxxxxxxxxx

hi emma and rob
it was nice to see you down in kent.so i thought i would have a look a the web site.Its really nice.
thinking of you all.

Love George

good for you beverly
i will think of you round hyde park and you can think of me round birmingham!!!
lets hope between us all we get some good money in...
michelle

i first met molly at my sisters party with Emma and Rob.Molly held my hand and we went on the bouncy castle together she was happy and beautiful little girl.I am running the Hydro womens challenge at hyde park and my charity for mollys fund.I just like to say i was proud to have known you Molly xxx

Isn't Molly just an inspiration to us all? Courageous and strong, she fought through and i think she is very special, she brought tears to my eyes.

Thank you to Michelle and Emma who point out that dozens of people have left comments about Molly and "Child in a Million" on several viewers' forums.



Here are few links. You may need to copy and paste them into your browser:



http://www.tvthrong.co.uk/child-in-a-million/new-series-child-in-a-million



http://www.unrealitytv.co.uk/reality-tv/child-in-a-million-molly-and-tahlias-story/



http://www.digitalspy.co.uk/forums/showthread.php?t=541420

please all click on photos in gallery as they will not be blurry and enlarge to a better image
ROCK ON WE WILL BEAT WILMS

Hi. I watched Molly in "child in a million", and couldn't help crying at the end. She appeared to be a very 'bubbly' girl and I loved her the first time I saw her. I couldn't help smiling when I saw her face. She was so brave and allways had a smile on her face. I didn't at all expect her to be taken away so soon. Thank you for making this site, so I can see pictures of her and donate money. Thanks XxX

Where do you start, Molly was part our life she is missed so much words cannot explain, the pain the hurt and the sorrow is all to much to bear, but through her death we have to find the strengh to carry on as this is what she would have wanted. Every minute every day you are in our thoughts and we promise you Molly that we will look after Mummy Daddy and Megan.What a wonderfull website it could not be more fitting, congratulations to Keith it's perfect for our little princess. Molly you have touch the hearts of everybody that saw a little bit of you on A child in a million, you will never ever be forgotten.xxx

Although I never met Molly, I feel like I knew her a little because I heard so much about her from her aunt Karen. Her spirit and her story touched all of us so much. She seemed so strong and appreciative and full of joy. This is a wonderful site. Thank you for sharing a little bit of your princess with us.

Well! Where can I begin? Molly was an inspiration to us all. Many people have dealt with death in there lifetime but to lose a child so young is inconceivable. Molly fought like some adults couldn't, she laughed when some adults couldn't, she brought joy to her family and everyone she ever met. Molly's story on 'child in a million' must have touched all those who watched it. God Bless Molly xxxx Emma & Rob I think of you a lot as many do.

I have thought about you all every day since the television programme. I now donate monthly to GOSH and cannot wait to begin donating to your charity. I hope the support you receive brings you strength, hope, and the wonderful knowledge people are now donating to charities they may not have before, because of Molly. this message comes with my love and best wishes. i will support this charity forever more

I didn't know Molly personally, but I know her aunt Karen from a special internet site, and through her, I feel I shared a teeny bit of Molly's amazing life, strength and the joy she brought to her family. I think it's amazing what incredible gifts we pass along to our children and they reflect all our goodness back to us in the moments they shine. Anyway, from the U.S. to the U.K., I want to extend my support and pray that sites like this one can help bring about the earliest possible detection.

Molly touched us all.

Hi there, I'm Molly's Aunty Karen, and I'm very proud to say that too! Molly was an absolutely inspirational child. Since the day she was born (2 days after my wedding!) she was a pure joy and ray of light in our lives, and that ray of light will shine on us forever. Anyone who saw the programme child in a million will know why we are all so committed to raising awareness of Wilms. I can't begin to explain how much we all miss our Molly, so we must fight on for all the other famillies out there who are suffering now, or may suffer in the future from this disease. Well done Rob, Emma and Keith for creating this site!

hi there
well we are good few weeks on now since molly was on tele..still crying..my thoughts go out to emma rob and megan,and all molly's family.
after watching the show,the next day i called gosh to see what i could do to help raise funds.
i am going to do the hydro active run in birmingham in september...
i am doing this in honour of dear angel molly and for gosh...
i am doing race for life in june for cancer research too...all helps...
but now that i know this is set up also i will await the site to be in full swing and will donate here too....
it is very important we help these amazing places.like gosh....and also raise awareness to wilms too...i had never heard of it....
all my thoughts and blessing to the family....
michelle

Alan who left the messages on reality thank you for bring this website to the attention of everyone check out the calendar we are raising money for molly wilm research and need sponsors rob and I are taking part in the bike ride (god help us) and at least 20 more please forward the website to as many as possible we need help and we will be setting up a web page for donations once we have the charity registered
once again thank you for caring you are a star!

We would like to thank everyone for their kind words and support this website was created by my brother Keith who like all our family and friends want to try and find a cure for Wilms or an earlier detection, as Molly was an extremely healthy child up to her very late diagnosis.
We are very proud parents and will not stop until Wilms is a recognised child cancer and in honour of Molly we will fight on...........................

After having just watched a programme that I recorded on 22 February 07, "Child in a million" I felt the need to send my deepest and most sincere condolensces to Molly's parents. Molly's beauty, both inside and out shone through. She must have been an absolute joy to be around, teaching all those around her how to be so brave and strong. I hope that your new daughter brings you as much happiness as Molly did in her tragically short life. I will never forget how much your family has touched my heart. May God bless you all..xx

Hello there

I just wanted you to be so kind and foward a message to Molly Biederman's parents. Like many people watching the programme, I have been so touched by this story. And this is reinforced my willpower to complete the London Marathon for Cancer Research this year

I am doing this also in memory for Molly! What an incredible little girl!

You can find my website information under:

http://www.justgiving.com/chantal_for_cancer_research

My best wishes and thoughts are with Molly's family

Thank you

Chantal Smith