Pseudomyxoma Survivor: Guestbook

From: Liz Oliver (Fri 27th Jan 2012 at 17:40)

I lost my mum to PMP nearly a year ago she had fought it for nearly 10 years and the one thing I would say is keep on at hospitals etc. There is not enough knowledge about this terrible disease our local hospital knew very little about it. Keep up the good work trying to raise the profile of PMP.

From: Leonard Million (Mon 16th Jan 2012 at 22:05)

I was diagnosed with this disease in 2009 and have been watching it almost ever since. I have been taking chemotherapy for about a year now, in between bipass surgery. They watch a tumor marker which starter at 3 and is up to 9 now. Its great to have you out there and hopefully the research will find a cure before the desease gets us. Thank you for the site.

From: Penny Duke (Sun 27th Nov 2011 at 00:52)

Hi Dawn.
When Roy got struck with PMP we had never heard of it and it was overwhelming. All the work you are doing is just great .. incredible.. you are an angel from above. It is so helpful to have a resource and an ear to lend . I am really impressed. Love your website too... great job with the colors and graphics. :)

From: Catherine Burgess (Sat 26th Nov 2011 at 23:17)

You should be very proud of yourself for setting up this charity. I lost my Dad to PMP just over 7 years ago when I was 15 years old. It is an evil disease and we need more people fighting to find a cure. Well done Dawn! x

From: Caroline Glynn-Ireland (Tue 22nd Nov 2011 at 23:32)

Hi Dawn I would like to thank you so much for all the hard work you are doing with this oragization. You are an inspiration to all other pmp suffers. Please keep up the good work.

From: Regina Gilchrist Ash (Tue 22nd Nov 2011 at 22:50)
Website: http://www.caringbridge.org/visit/ash

Wow, Dawn, what a site! Much needed and you are such a go-getter, girl! Are you gonna slow down after you and Jay get hitched in Jamaica? ;) My other half is scheduled for his second MOAS on Dec. 29 and the stress is starting to weigh, so think of us, send prayers skyward. Thanks, again, for all you do, luv!

From: Kelly Geltmeier (Tue 22nd Nov 2011 at 10:06)

This site is needed. You saw the need and have provided all of us with a bright, cheerful, invaluable resource. You have provided us with a place to share our stories, ask our questions, and get involved to promote awareness. Way to go Dawn.

From: Therese Surges (Mon 21st Nov 2011 at 10:57)

Dawn, you are an amazing woman. Through your own fight you have managed to create such a wonderful organization all in the name of love. It takes an extraordinary person to work as hard and diligently as you have and good things are happening as we speak. Keep up the good fight and THANK YOU from the bottom of my heart for fighting for others with your disease as you do.

From: Gail Arakelian (Sun 20th Nov 2011 at 23:03)

Dawn, you are a such a wonderful spokesperson for us. Thank you for all of the your hard work you do to try to raise awareness of this horrible disease. The ONLY good thing about PMP is getting to meet the amazingly strong people in our support groups.

From: Sue Spain-USA (Sun 20th Nov 2011 at 15:57)

Your website and Facebook page have been a godsend to all PMPers that find support and wisdom there. The help and awareness you have provided are immeasurable to all of us! Thank you, Dawn, so much!!

From: Shaohui HUANG (Tue 1st Nov 2011 at 12:45)

i am chinese.
I was diagnosed with Pseudomyxoma peritonei in Oct 2009. and had twice surgery.

i need you help.but how can i contact you with email?

From: Carl (Wed 26th Oct 2011 at 00:52)

Hi Dawn,

Thank you for your continued support. My mum is presently in Basingstoke. Her operation was one week ago.

Your texts with messages of support are very much appreciated.

From: ELAINE HALLIGAN (Mon 24th Oct 2011 at 19:18)

Hi Dawn I think you are amazing you have been through so much. My mother recently was diagnosed with pseudomyxoma in her ovary she had a full hysterectomy and appendix and omentum out, the cyst had ruptured but for now she doesnt need chemo, I had never heard of this disease it was very scary not knowing anything about it. She will be scanned every 3 mths if it returns it will be on her small bowel we pray this doesnt happen. She is 61, her symptoms began in jan/feb, by may she looked 7 mths pregnant but was losing weight everywhere else, she lost nearly 4 stone in all after op in july.It is reassuring reading this and knowing we are not alone.

From: kelly gilchrist (Fri 26th Aug 2011 at 14:34)

Hi dawn, i am so proud of you, in what you are doing to make awareness, you are a strong beautful women with an amazing family. Keep up the good work you are doing,be stonge and keep well.

Kelly

From: sam hill (Sun 24th Jul 2011 at 10:34)

Hi Dawn,
Just wanted to say hi and glad you're doing well. I saw you in Basingstoke in June 2008, you were in the same ward and bay as my aunty Pat, who is a fellow pmp survivor. She told me about your website and all the incredible things you are doing to raise awareness. Also to let you know she is fighting fit and has made a full recovery.
Keep up the good work xx

From: karen Labrum (Wed 20th Jul 2011 at 19:38)

I met a lovely lady today while i was in kettering general hospital. She is the bravest person i have ever met.

This ladies name is Dawn Green, It is an honour to make your acquaintance.

From: Julia McCullough (Sun 26th Jun 2011 at 22:06)

HI Dawn
What a total inspiration you are!!
I too was diagnosed in June 2006 with PMP after an operation that was suspected ovarian cancer which turned out to be PMP! I was then referred to Brendon at Basingstoke and in Jan 2007 had MOAS lasting thirteen and half hours to remove the mass, it was a really tough recovery after a few complications and developing sepsis but with lots of excellent care by all the nurses at Basingstoke hospital and of course lovely Sue Elves and her team i made a remarkable recovery. I wouldnt be here now if it werent for them, i owe so much to them and would love to offer support in helping you raise funds! I have been having yearly CT scans since my surgery and my latest one in May this year has shown a slight return of the disease! I have every faith that Brendon and that he is managing me very well and he has reccomended i have another scan in Oct. Thank goodness for survivors like you who have the drive and determination to put this disease on the map and go onto helping support other fellow sufferers!! You of course know the importance of having the total support! It can be a lonely experience as it is still so rare, great website keep up the great work!!
we are all behind you!!
take care Julia xx

From: PMPawareness (Thu 23rd Jun 2011 at 18:07)
Website: http://www.pmpawareness.org

Dawn:

Over the past several years our little community has grown by getting the word out or as we put it awareness. You have done so much with so little to spread awareness in the UK with very little resource, you have over come and adapted to any and all obstacles in your way, you're truly amazing. Keep up the good work.

From: Lynda Meador (Thu 23rd Jun 2011 at 16:39)

Dawn, thanks for being such an outgoing advocate for this horrible disease called PMP! Your delightful enthusiasm, dedication and awareness is contagious. Keep the word going through your site and your presence in the public forum...we need advocates like you!

Blessings,
Lynda

From: Joanna (Thu 23rd Jun 2011 at 16:38)

Thanks for being here and providing this support network. I absorb all I can and hope to some day have something big to give back. I'm cancer-free for 1 1/2 years and going strong.

From: Debbie Dunham (Thu 23rd Jun 2011 at 15:05)

Thank you so much for starting this site. We can never have too many sources available. There is not enough known about this horrible disease. I am coming upon my first anniversary of being CA free. I pray that it continues and that someday there is a cure for all of us.
Thoughts and prayers for all of us (survivors and newly diagnosed.) Again Thank You.
Debbie

From: laure morgan (Thu 23rd Jun 2011 at 08:55)

Dawn your a star, thanks for all your help you really made a difference and gave me hope, its so nice to know your not alone, I really hope to come to your party xxxx

From: Barbara Kane (Thu 23rd Jun 2011 at 04:22)

Hi Dawn, Thanks for setting this up. It's a fantastic source of info, and it helps to know that we're not alone.

From: Leigh Ann Matthews (Thu 23rd Jun 2011 at 03:53)
Website: http://www.caringbridge.org/visit/chadmatthews

Dawn, I can't imagine life without you. I'm so glad we met, but I hate the circumstances. You are a true fighter and so inspiring. Keep going! I wuv you mate, all the way in South Carolina, USA! :o)

From: Pat (Thu 23rd Jun 2011 at 03:17)

Dawn,

Thank you for speaking out on behalf of us your fellow PMP survivors. Your Web Site is beautiful, as you are. Keep up the good work.

Luv U xoxoxox

PatB

From: Scott (Thu 23rd Jun 2011 at 01:53)

Hey Dawn what you have done in the past year has been amazing, you arebtruely a force to be record with in the fight against PMP. Keep it up!

From: Joy (Thu 23rd Jun 2011 at 00:15)

Thank you Dawn for all that you do to raise awareness and for your efforts in giving us all support. You are a true survivor in every sense of the word. So glad to be part of this amazing support system we have for eachother. xxxx ~ Joy ~

From: Kathleen Severs (Wed 22nd Jun 2011 at 23:46)

So many appreciate all you are doing to raise PMP awareness and funds for research. Big hugs to you and your family.

Kathleen Severs
Arlington, VA
USA

From: Judy Engel (Wed 22nd Jun 2011 at 22:50)

Thanks Dawn for your time and interest in providing a place to help those diagnosed with PMP and other types of appendicel cancer.

From: Mary (Wed 22nd Jun 2011 at 22:37)

Thanks for you unending efforts in fighting this terrible disease. Making all in the medical community aware that it can be controlled is key to our survival.

From: Hope Potter (Wed 22nd Jun 2011 at 21:57)

Thanks Dawn!! You are certainly one in a million for far better reasons than PMP! Thank you for all you do!

From: Deborah Warner (Wed 22nd Jun 2011 at 17:40)
Website: http://secretcancer.com

Thank you, Dawn, for creating a place where we can find information and support. I felt very alone with this terrible disease. Through you, I've found an international community that understands. You are an inspiration!

From: Bill Brook (Wed 22nd Jun 2011 at 16:05)

Thanks Dawn for setting up this fantastic site and the facebook group ! It really helps to be able to share information in this way, and hear from people who have already 'been there, done that, bought the T shirt' !!

From: Don George (Wed 22nd Jun 2011 at 16:00)

Hi Dawn
The work that you are doing is imeasurable you are paying it forward in so many ways. Please keep up the good work but save some energy for yourself as you need to stay as healthy as posible to do the work that you do.
don't forget family.
Hugs & Love
Don & Thea
Sharon, Ontario, Canada

From: Diana Lentz (Wed 22nd Jun 2011 at 15:45)

Thanks Dawn for all you are doing to bring awareness to this dreadful disease. Keep up the great work!

From: Lynda Kludt (Wed 22nd Jun 2011 at 14:51)

Dear Dawn,

Thank you for all that you do to raise awareness of this horrid disease! I am soo glad that you remain a strong, awesome survivor!!!

I am a 4 1/2 year survivor of well differentiated cystadenocarcinoma of the appendix with PMP. So far, my prognosis remains favorable!!

Thanks again for all that you do my friend!!! xxxxxx Wish I could come to your party in October!!!!!!

From: Therese Surges (Wed 22nd Jun 2011 at 14:41)

Dawn, you are an inspiration to so many and definitely give me hope for my husband who is in the middle of this horrific disease. What you do to help everyone despire your own battle is a beautifult hing! God Bless You!

From: Alice (Wed 22nd Jun 2011 at 14:35)

Dawn, thanks for sharing information about our rare cancer. To many more years of friendship!

From: kristi k counter (Wed 22nd Jun 2011 at 13:59)

You are wonderful!

From: Meredith Meilleur (Wed 22nd Jun 2011 at 13:50)

When they said I had a one in a million cancer, I felt so alone. Everyone one knows someone who knows someone who has breast cancer, lung cancer, etc. But when I told people what I had been "blessed" with the response was always "pseudo what?"
Finding a support network has been a godsend. Sharing information and inspiration makes the rough times not so isolating. Knowing there's someone to talk to, even if they are half way around the world, is so comforting.
My PMP brothers and sisters are there for me whenever I need to compare symptoms, treatments, or ask for a virtual hug. Thanks Dawn!

From: Michael Dvorsky (Wed 22nd Jun 2011 at 12:44)

Great job and keep up the good work. The more information the better we all are in fighting this disease.

From: Fiona Walkley (Wed 22nd Jun 2011 at 12:05)

Thank You Dawn for all of the information you give us all and for your amazing support.
I never thought I'd know anyone with this let alone an amazing woman like you.
Thank you.ox

From: Helen B (Wed 22nd Jun 2011 at 11:02)

Dawn, thank you for putting together this website, and sharing your story. Cancer is hard for anyone. Having a rare cancer, where there is little information about outcomes / treatments is tougher still.

Being able to find others in the same boat makes things more manageable. Keep up the good work, and best of luck for "unremarkable" scans :)

From: Kelly Geltmeier (Wed 22nd Jun 2011 at 10:51)

Thank you Dawn for creating a place where I could find answers and support for this very rare cancer. When I couldn't get a clear answer from my doctors because they really didn't know, I received enough information and resources from this site that helped me educate them in some cases. I had surgery in a land where I didn't understand the language, this site gave me the peace and confidence I needed to fight and continue to fight. You are a very special woman for fighting this cancer, but more for having the vision to see that education is needed about this horrible disease.

From: Jeff Wilson (Wed 22nd Jun 2011 at 10:00)

Very worthwhile and helpful site. Nice for my partner to also have a network of friends who understand what she has been, and still is, going through. Thanks Dawn.

From: Bobbie Tania Kay Le Page (Wed 22nd Jun 2011 at 09:33)

Dawn, you are an inspiration to us all and help us to feel we are not alone. Please keep up the good work. ♥

From: Charlotte (Tue 21st Jun 2011 at 23:11)

Thanks Dawn for your support and info on this website and other sources! They really have been invaluable and its great to know that we all have each other for support! Keep it going! XX

From: Bonnie (Mon 25th Apr 2011 at 20:32)

I am so excited about this website! I was diagnosed in Oct. of 2006 with PMP. starting in the ovary. I had two surgeries, the first being a total hysterectomy and removal of the omentum. The second surgery was in June of 2007. Then, my appendix, spleen, and a portion of my stomach were removed. My liver and diaphram were scraped and heated chemo was done. I thought I was going to have to go to Washington D.C. or Texas to have the surgery but I found a Doctor (wonderful man) right where I live, University of Cincinnati Hospital in Cincinnati, Ohio, U.S.A. I also tried to do research on the web. Sure wish your site was available then. Part of what I continue to deal with is the feeling that I am alone. Dawn, when I read your comment about having no belly button, I laughed and felt I now belong. I am so excited about the bracelets and your efforts for fund raising and research encouragement. Thank you, Thank you. Do you know of anyone in the states that have PMP? I have yet to actually meet anyone.
Thanks again for your efforts,
Bonnie

From: Shell (Fri 15th Apr 2011 at 21:48)

Hi Dawnn, you are being kept very busy. I'm doing well in hospital, feel much better anyway, had dangerously low potassium levels and they are picking up. This is my first day getting back into some internet stuff.
Keep up the good work.
shell

From: Tracey (Thu 7th Apr 2011 at 22:19)

I found out Jan 2010 i had pmp after my appendix and ovary were removed. I had the MOAS at the Christie (who are all fantastic especially my specialist nurse Bex) My op removed Gall bladder, spleen, belly button, stomache lining, remaining ovary, full hysterectomy, bowel cleaned up and diaphram and liver shaved. I am just awaiting more results from latest CT scan and can say im more than a little nerveous, so it is a relief that i have found this wonderful site where experiences can be shared by people who are suffering from this rare cancer, thank you.

From: Tracey (Thu 7th Apr 2011 at 22:18)
Website: http://www.facebook.com/profile.php?id=516938223#!/profile.php?id=1198383247

From: Andrea (Mon 4th Apr 2011 at 19:13)

Hi found out I had pmp last June 2010 after having my appendix removed in March, finally had the operation in November 2010. I have had my Gall bladder,belly button and full hysterectomy removed. Had the operation at The Christie and I have just returned to work.Getting on well but still under the Christie for 5 years having scans and blood tests.

From: dawn penfold (Sun 3rd Apr 2011 at 17:49)

hi dawn thank you ever so much for your help, it was good to finally talk to someone that understood what i had been through and what i'm still going through. it help drag me out of a very dark place xxx

From: PAMELA THOMAS (Sat 19th Mar 2011 at 11:13)

Dear Dawn.Thankyou for your write up in the daily express.
I had pmp in 2009 and just like you when it came back in 2000 they told me they cant do any thing and I was going to die.But my story was like you, had to search the internet as I wanted to see my grandchildren grow up.
But had the moas with Brendon and 10 years later with scan every year I am still free,Hope this gives hope to some people just starting out.

From: Claudia Drake (Thu 3rd Mar 2011 at 11:51)
Website: http://www.pelicancancer.org

Dear Dawn,

Thank you for your inspirational work on fundraising and awareness-raising for this very rare type of cancer.

For those who would like to find out more about Mr Brendan Moran's work at Basingstoke, please feel free to link to the Pelican Cancer Foundation's website:

http://www.pelicancancer.org/index.php?menu=1&submenu=104&page_id=107&page=pages

All power to you!

From: dawn green (Tue 1st Mar 2011 at 20:30)

Thank you Dawn for being such an inspiration to others who may be experiencing cancer. Having had a similar experience myself 3 years ago it is great to see your strength and positiveness shining through via your website, brilliant xx

From: Charlie Walker (Tue 1st Mar 2011 at 13:47)

I was diagnosed last June with PMP. I have been unbelievably lucky because the cancer was confined to my Appendix; it had not burst and had not spread. My diagnosis was completely by chance and I had no symptoms at all. Somehow after a routine medical I was referred to Mr Satvinder Mudan in london. He immediately operated and removed chunks of my insides but the biopsies revealed that it was just in my appendix (which was huge!). What was thought to be a grim prognosis just turned out to be just post operative care.
Who knows what the future will bring but at least I can consider a future. I have been blessed. I am so sorry to all of you who have not been so fortunate.
My GP had never heard of it - and that probably goes for the vast majority - he only put in my medical records an entry "appendix operation" - so he obviouly learned a lot from my experince! Whilst there continues to be such ignorance and lack of care this nasty illness will continue to go undiagnosed.
I wish you all the very best wishes in your battles, and support and love from those you are close to.
The more knowledge of this the better the chance of others to be as lucky as I have been.
Charlie

From: Steph (Sat 5th Feb 2011 at 22:42)

Bless you Dawn for being a help and inspiration to others. X

From: Melanie Dix (Thu 20th Jan 2011 at 20:38)

I would just like to say a huge thank you to Dawn for all your support recently. It has been an emotional rollercoaster with my mums health but she is doing really well in herself at present. Your website provided us with some valuable info and you provided alot of support via email and facebook. I think you are an inspiration to others Dawn and I really hope this charity takes off as you have made a huge difference to me as someone who until a few months ago had never heard of the condition. Many of the large and well known charities started with one persons vision and passion to support others who followed them. Good luck with everything, you deserve it. Mel x

From: John Cole (Mon 17th Jan 2011 at 13:00)

Hi Dawn

Thank you for your website and for guiding me through to The Pelican Centre and Mr Brendan Moran who was instrumental in the correct diagnosis and prognosis for my rectal cancer. I wish you all the best for the future and keep up the good work.

From: lauren (Thu 13th Jan 2011 at 10:38)

hi there i am a 28 year old who has been diagnosed with pseudomyxoma peritonei i am having surgery in feb and am so frightened, i have a 9 month old so who i will have to leave for a few weeks whilst i have this done, just want to hear any sucess storeis and know im not alone xxx

From: Colleen (Sun 26th Dec 2010 at 03:30)

Hi I am from OZ had my last op in June of this year am doing great and am looking forward to 2011. This is a great website will be bookmarking it so I can return

From: Jonathan Darby (Fri 10th Dec 2010 at 11:07)

Keep up the good work!

From: Michelle (Tue 7th Dec 2010 at 09:08)

Hi Dawn

I am in Australia and sitting in my loungeroom waiting for the operation for PMP (no known date as yet). I was researching fatigue and PMP and I come across your website somehow. Its given me a boost in a situation when I know I am deteriorating but unsure when I can have the operation. I have a caringbridge website to share information about my condition and operation with family and friends, will put your link on there. I have a sister and niece in England and hoping they can help your fundraising efforts. Well done.

From: Stuart Amblin (Tue 23rd Nov 2010 at 19:41)

Fantastic website. My wife, Samina had the big op after her cancer diagnosis at the beginning of this year. She's now recovering well. We'll be glad to see the back of 2010! Feeling positive for the future.

Stuart Amblin

From: Joanne Slade (Mon 8th Nov 2010 at 21:49)

I was there the day the phone call was made. It was awful Dawn was almost told to go home and die. Research on the internet and a positive attitude led to there being a light at the end of the tunnel. Opperation after opperation, feeling like it would never end, Dawn came out fighting for her children. Dawn always said "i can't go, I have my girls". It was heartbreaking to watch this but words from the fighting women has meant she is around today, full of life and an inspiration to anybody that has this shocking awful disease. You have one life, live it to the full xxxx Proud of you Miss Green!

From: teresa orourke (Sun 7th Nov 2010 at 18:21)

What an AMAZING Lady you are,,
You deserve the BEST,Dawn
Wishing You Love Peace and Happiness,
Teresa x SPAIN

From: Michelle Sanders (Sun 31st Oct 2010 at 07:29)
Website: http://www.caringbridge.org/visit/michellelafferty

Dawn you are such an inspiration, I for one look up to you greatly, we all think we would like to do something to help but you went out and did just that. Thankyou so much
Shelly xx

From: June Finn (Sat 30th Oct 2010 at 15:24)

Hi Dawn - congratulations on the setting up of your website. There is lots of information which will be a Godsend to those just newly diagnosed with pmp. I know I would have found it invaluable. Your website in no way detracts from the Christie site forum. The more info available the better. Keep up the good work. I just wish I lived closer to come to some of your fundraising events but, who knows, maybe one day.

From: Deborah Hatcliffe (Sun 24th Oct 2010 at 20:41)

Well done Dawn!
What a fantastic website. Great to see our own logo, wristbands and car stickers. Had I not been diagnosed with PMP I would still never have heard of it today,its a rarely known cancer and a complete mystery to some GPs and hospitals.
My PMP was discovered in March 2009. I had the MOAS in June 2009. Five weeks in Basingstoke - could not fault the care- and first year's Scan and blood tests were in June this year. All clear!!!! Met Dawn thru Forum and we were in hospital together at Basingstoke. Its great to have someone to share your ups and downs with which isnt easy when you are one in a million!

From: julie keen (Fri 22nd Oct 2010 at 20:56)

Hiya Dawn

I just wanted to say how lovely it has been for me to be in touch with Dawn. I was diagnosed with PMP in June 2002 and had the MOAS in January 2003. Since then I have been quite isolated, only being in touch with one other sufferer. I recently contacted Dawn and we have talked loads about our condition and she has introduced me to other people she has met with PMP. It is so comforting being able to talk frankly with someone who knows exactly how you feel. It's not always easy to talk to your family and friends about all the weird things going on in your mind, so finding other PMP sufferers to speak to is invaluable. After speaking with Dawn it made me realise that we may not all suffer the same symptoms as each other and the path our illness follows is never the same a the next person's but all the feelings and emotions we go through are more or less the same. Therefore, we must all stick together and support Dawn with this fantastic website!!

lots of love julie x

From: hayley burgess (Fri 22nd Oct 2010 at 12:09)
Website: http://www.marktudorphotography.com

Hi Dawn,

Id just to like to share with everyone how invaluable you have been to myself and my family over the past couple of months. My father in law has been diagnosed with pmp and found out yesterday he is a candidate for surgery (moas) in january. Without your calming influence, guidance and support I really dont know how we would have remained sane.
I found relative "down to earth" and most importantly "honest" information extremely hard to find and when I thought I had, I found it quite hard to decifer and digest.
Your story shows one womans struggle to not only accept an illness but also face it head on, fight like an absolute trooper and come out the other side not only on top and a winner but an absolute inspiration to so many others! Not only have you had your world turned upside down once, its happened twice, which to me is inconceivable but somehow you have faced it and are still here willing and wanting to help others in their journey they may be about to undertake.
I wish you all the love and luck in the world with the success of this website, it really has been a possible life saver for us and no doubt will be again in the future to other families.
May the angels watch over you, your family, all other pmp soldiers and families now and forever!
hayley xx

From: Dee (Wed 13th Oct 2010 at 14:00)

Hi
Well done have managed (tough for me as not technical!) to donate the �30 my daughter raised this year doing 10k race for life./ I am aPMP survivor of one year now!!and very pleased to be here. Keep up the good work

From: jeff unsworth (Sat 9th Oct 2010 at 11:02)
Website: http://www.rosiesstory.co.uk

well done Dawn.
good start.Would it not be an idea to show how you are doing with the donations. ie a thermometer type sign, or something to show how far away you are from your goal?
x

From: Garry Nash (Tue 28th Sep 2010 at 16:14)

i spoke to jay at work and he told me about your website,you are a real inspiration to us all,i will buy some wristbands next time i see him, good luck with the fundraising.

From: John Sime (Tue 28th Sep 2010 at 15:39)

Well done Dawn. I have a vague recollection of seeing you around C2 last June. I was just being released after 6 bad weeks, 4 of them in ITU. All well now.

From: Joyce Young (Sun 26th Sep 2010 at 22:48)

My husband was diagnosised in July of this year, he had surgery on Aug. 23, however the tumor was to large, and he's now recuperating from that surgery, as soon as the incision heals completely he will start chemo for 3 months, and hopefully @ the end of the 3 months he will have the surgery again. Thank you so much for your website!

From: Karis Millen (Fri 24th Sep 2010 at 21:35)

the website amaziing xx i have a wristband and i support!!

From: Nicky Painter/Green (Thu 23rd Sep 2010 at 12:03)

Well done you Dawn! Good luck with the fundraising, you really are a superstar, lots of love from the Greens in Crawley. x x x x

From: teresa (Wed 22nd Sep 2010 at 18:35)

brillant website mate very proud of you photos are lovely

From: Keith Booth (Wed 22nd Sep 2010 at 18:30)

I've recently been diagnosed with PMP. It's great to see a site dedicated to information about this rare cancer. I'll certainly keep keeping in touch for updates.

From: Kevin Graves (Fri 17th Sep 2010 at 15:16)

I am a 4 year survivor of PMP. I am very excited that another website has been set up to raise money towards developing a cure for this terrible disease. Thanks for all your hard work. I will be making a donation shortly. We all need to keep on fighting!!

Kevin

From: Ann Brown (Fri 17th Sep 2010 at 03:43)

Dawn,your website is wonderful. I enjoyed all of your photos and videos. I am so proud of what you are doing. You are such an inspiration to me. We have to let people know about our cancer. I am facing so many problems with my PMP. It is now in my lungs and I am searching daily for help since I was told there is nothing else that can be done. Thank you so much!!!

From: Stuart Eaton (Wed 15th Sep 2010 at 20:44)

Hi little sister you looking great now hard to believe how far you have come in such a short time an for the appeal i know you`ll get there cause you dont know how to give up luv ya loads xx

From: Rebecca Dowen (Sun 12th Sep 2010 at 21:27)

Well done hun, you've done an amazing job of setting up this website and I hope you continue to raise awareness about this terrible cancer.
You are a very inspirational person.
xxxxx

From: Sarah Pearson (Sat 11th Sep 2010 at 09:25)

Such a positive website...good on ya girl! We knew each other before different cancers had such an impact on our lives...you are an inspiration and help to others always. Thank you x

From: Kay Finnis (Sat 11th Sep 2010 at 03:28)
Website: http://www.keeshamist-pmp.blogspot.com

Well done Dawn!!
The good part about this dreadful cancer is "meeting" people like you from all over the world!

There are just too many PMP Angels to watch over us now ... the latest being our dear friends Ginny & Julie within days of each other! May they continue to watch over us pain free and smile down upon us!

It is people like you who are determined to spread awareness who will make a difference to those battling this disease and those yet to be diagnosed!

Keep up the great work amazing lady!!
Huge Aussie hugs,
Kay
PMP survivor since 2001

From: Anne Dunn (Tue 7th Sep 2010 at 23:03)

Good on yer Dawn - I will help all I can towards our cause.

We met because of this horrible disease and have become great friends - let's raise �5,000 and become an official charity in memory of Julie xx

From: julie keen (Tue 7th Sep 2010 at 17:18)

Dawn

Well done you!! From another PMP sufferer who always means to do something like this but never gets around to it - you are a true inspiration!

julie

From: jayne taylor (Sun 5th Sep 2010 at 20:40)

Dawn we met through PMP and have become really good friends, you have done a great job setting up this website to help others and i will give you any help and support i can !

From: JEFF AND ROSIE (Sat 4th Sep 2010 at 17:59)
Website: http://www.rosiesstory.co.uk

Well done Dawn.

Rest assured we will donate to your site for the same reason you set this one up. Keep up the very good work girl.
love and best wishes,Rosie and Jeffers xx

From: Wendy Knapman (Fri 3rd Sep 2010 at 18:12)

HI Dawn

You've done a fantastic job on this site and good for you for helping others in a similar situation. Heres to reaching your goal of a registered charity.

From: Sharon Brown (Tue 31st Aug 2010 at 20:46)

To all the Pretty Marvellous People especially Julie, It is difficult to see beyond the sorrow but the fond memories will always shine through like the brightest star, x x

From: Julie Rogerson (Tue 31st Aug 2010 at 09:58)

Well done for getting this up and running Dawn. PMP is such an awful disease which claims so many wonderful people. This website is a fantastic idea to raise awareness in the hope that people will learn to recognize the symptoms and get treatment sooner before the disease really takes hold. I am happy to donate, after all I wouldn't be here either without the kind donations of others funding research into PMP. Well done other pea to my pod! Julie x

From: Ellen Orbell (Tue 31st Aug 2010 at 08:48)

Weldone Dawn you have done well, keep it up and think of all those you will be helping, Just a smile from you helps me lots of love MUM xxx

From: Karen Smith (Mon 30th Aug 2010 at 23:23)

Hi Dawn

Congratulations for doing your website, I didnt know I was treating a celebrity (had a look at your links) ha ha!! I look forward to helping you keep your wonderful, positive attitude for your LIFE!! You are an inspiration for other people out there and as I've said before, you radiate hope xxx Well done :)

From: Katy Parker (Mon 30th Aug 2010 at 22:42)

WOW go you! Very impressed with this mate well done and keep up the good work mwah xxx

From: Nicola Tait (Mon 30th Aug 2010 at 21:58)

Congratulations on such a great website that will bring support and help to others, you certainly are one in a million xxxx

From: Michelle Sanders (Mon 30th Aug 2010 at 20:45)

Dawn you are certainly one in a million, keep up the good fight and good luck with the fund raising xx

From: Martin Leivars (Mon 30th Aug 2010 at 19:32)

WELL DONE BABE & GOOD LUCK!!!!

From: kirsten Marshall (Mon 30th Aug 2010 at 19:25)

Hi mum congrats on setting up this fantastic website to help others around you !!

From: Steve Treweeks (Mon 30th Aug 2010 at 17:54)

Very best of luck with the new website
Dawn, so very impressed! Go girl! Bumper xxxx