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'Ain't No Mountain High Enough'

£5,465 of £5,000 goal

Raised by 167 people in 11 months
Created August 16, 2018
Hello beautiful people! On the 20th of October 2018, a collaboration of amazing human beings, dressed in their finest sequins, are climbing the highest peak in Wales, Mount Snowdon. We need as many of you beauts in the world to reach the top with us, so anyone and everyone is requested to join us in this quest.

We are trying to raise money for a fellow disco, life loving woman who needs our help. By doing this adventure together, we are raising awareness of this sad illness, not only for our mate Anna, but for others in the UK who cannot receive the vital treatment that she desperately needs.

Anna has a brain tumour that cannot be operated on in the UK, and we need as much help as possible to save her life. Please read the link below for her story...

Our plan is to get the masses of music, fun loving, wonderful friends that we are all fortunate enough to know, to donate as much money as possible, and to invite as many future friends to come along and join what will be one of the most unique charity raising events we can think of.

So far we have approximately 50 comrades willing and signed up for the walk. It is a route that is not particularly hard, so not beyond average capabilities and health and safety has been taken into account. That said, It is still challenging; approximately 6 hours from bottom to top to bottom.

We have already booked accommodation for those registered so far, there are plenty of rooms/bunkhouses/hostels available which we can help guide you in finding in a beautiful town called Betws-y-Coed, at the base of Snowdon and accessible by train.

Weather permitting there will be a disco at the peak to celebrate our success... The worlds highest disco!!!!???

Obviously there will some form of afterparty to celebrate our success in conquering this mountain.

We are trying to get the Guinness book of records involved. We already have the press involved, a drone and a cameraman. We are hoping for as much sponsorship and publicity available to help make sequin history! Just by sharing this page, any love and assistance is sincerely welcomed. Combined as a team... There ain't no mountain high enough... ALL WE NEED IS YOU! x

Each climber is encouraged to raise or donate a minimum of £20 to take part in this event.

Thankyou xxxxx

Here is Anna story in her words...

To my dear family, friends, colleagues, fellow disco dancers, red-head comrades, acquaintances and anyone that has taken the time to read this:

 

As many of you will know, my health has been deteriorating quite considerably for a number of years. My problems started almost 9 years ago in my early 20s when I began experiencing chronic daily nausea and dizziness. After trialling several medications and having every test available, no-one could tell me what was making me feel so sick. Years passed with me doing my best to manage this horrible condition and then 2 years ago my symptoms started to get a lot worse.

 

I’d always suffered from migraine since my teenage years, but the attacks were only a handful of times a year and manageable with acute migraine medication. Around 18 months ago my headaches started to increase in regularity and severity and by the end of the summer last year I was struggling with agonising headaches every single day.  On top of this, I was experiencing nausea that wouldn’t respond to any kind of medication.

 

Then the vertigo kicked in. I’d suffered a previous episode in 2015 that had lasted for 4 months, but this time the swaying and blurred vision was so much worse and has never left me. By Christmas I was bed bound with debilitating daily migraines, nausea and vomiting, vertigo, regular loss of sight in my left eye, severe light and sound sensitivity, raging tinnitus in my ears, brain fog, forgetfulness and extreme fatigue.

 

I saw a neurologist early this year who diagnosed chronic migraine, migrainous vertigo and constant tinnitus. I was referred for an MRI scan of my brain as a precaution as we have a family history of brain tumours.  The results showed that I have a very large, 18mm pineal cystic tumour sat on my pineal gland deep in the middle of my brain. Thankfully these types of tumour are benign, but unfortunately large, symptomatic pineal cystic tumours are very rare and are not well understood, with many medical professionals dismissing all possibility that they can cause symptoms. Many would describe them as asymptomatic and an ‘incidental finding’ despite the debilitating symptoms being exactly the same and as severe as those caused by cancerous tumours.

 

Hearing the word tumour, benign or otherwise, made me want to find out more and after researching these types of tumours, I stumbled across an online support group for people who had them and discovered that almost everyone had exactly the same symptoms as I was experiencing. There were literally hundreds of people in the UK alone that were battling daily debilitating headaches, visual disturbances, vertigo, memory issues, tinnitus, nausea, dizziness, seizures, sleep problems and fatigue. It was from the information in this group that I found out that there are only 6 neurosurgeons in the world who currently remove them, and sadly none of them are based in the U.K.

 

Undeterred I set about sending my scans to any medical professional in the UK that I found mentioned tumours of the pineal region. I must have sent emails to at least 20 consultants. A number of them came back to me wanting to help but either they weren’t the right person and would refer me to someone else or they didn’t respond.

 

By this point I had tried 9 different medications for migraine, as well as a 12 week trial of a new kind of treatment, the Vagal Nerve Stimulator device. I’d also paid for private Vestibular Rehabilitation Therapy to address the vertigo but this made my excruciating head pain worse. I’ve seen a nutritionist, tried acupuncture, cranial osteopathy, kinesiology and every vitamin or remedy that I found or was suggested to me that could possibly help alleviate my symptoms but nothing has worked. I am now having between 13-20 consecutive days per month of the most excruciating head pain describable. They are so bad that my partner has wanted to call an ambulance on numerous occasions as he simply hasn’t known what to do. For the rest of the days of the month my head pain is still at a 7-8/10 in severity and nothing I do does anything to take the edge off the pain or any of my other symptoms.

 

I cannot tell you what it feels like to experience that level of pain for an hour, let alone weeks on end with no relief. The last six months of my life have been spent pretty much confined to the four walls of my darkened bedroom. I miss working, I miss socialising and having a purpose. I don’t remember what it feels like to be well. I haven’t worked since December and am worried I will lose my job. Over the past six months I’ve missed so many important life events of loved ones such as my sister’s wedding and countless other opportunities to spend time with my nearest and dearest. Missing out on these has been heart-breaking.

 

I have absolutely no quality of life. At times I have completely lost my mind and have felt like giving up.

 

Feeling pretty desperate, I decided to send my scans to three of the six surgeons in the world that do operate on pineal cystic tumours, between them they have successfully removed over 120. All three have said that the tumour is causing compression inside my head and could very much be the cause of my problems.

 

I got to speak directly to one of the surgeons for over an hour when he called me to discuss my scans and was able to ask lots of questions. He reassured me that I wasn’t crazy and that he believed the cyst was most likely the cause of my problems given its size and the fact that I had tried so many medications and treatments without success. He said that that there will be no relief from medication or any treatment as essentially there is something big in my brain that shouldn’t be there, pressing on things it shouldn’t. He also said my symptoms will only get worse, and I have definitely felt this over the last few months. I have spoken to six people at length who have had their tumours removed and their symptoms have 100% improved. There are several others in the support group who have spent over $100,000 travelling abroad for the surgery, often selling property, cars, jewellery and family heirlooms to do so.

 

Given that I have now tried everything and the NHS are unable to help me, I am hoping to raise £35,000 to cover the cost of surgery in Germany with neurosurgeon Dr Schroeder. The money raised will cover the cost of the surgery, hospital fees, accommodation, flights and anything I may need in the 3-6 month recovery. In the unlikely event there is any left over, I will make sure it gets to a fellow ‘Cyster’ as we call ourselves, or use the money to raise awareness of this rare condition. I am also writing to my local MP to raise the profile. The support group has been a real lifeline for me and I will always be there for anyone who finds themselves with this awful rare condition in the way they have for me.

 

Thank you so, so much from the bottom of my heart to those who donate, many of whom I will have never met and probably never will. You will be giving me my life back and I will never be able to thank you enough for that. I understand money is tight and I often see campaigns such as these wishing I could help so if you’re reading this, please do share this page as for me it’s just as much about raising awareness as it is raising funds. I truly believe that in time, this surgery will be provided by our wonderful NHS in the UK as there are surgeons here who are qualified to do it and a couple are interested, it’s just going to take time to raise awareness and I’m committed to do all I can to make that happen.

 

Lastly, I would like to say a HUGE thank you to everyone who has helped me so far, I would have given up a long time ago if it wasn’t for my incredible partner Peter, my amazing family, my superstar friends, compassionate colleagues and volunteers, fellow ‘Cysters’ (particularly super-cysters Charlotte and Gareth), Jay for the images, Dr Bulpitt, my neurologist as well as the other Drs and Consultants who have done their best to help me get better. Thank you so much for the cards, flowers, gifts, calls and messages, this could have been a very isolating journey but I am extremely lucky to have such unfailing, solid support behind me keeping me afloat. You’re the best, thank you :)

Anna xx
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FINAL PLEA FOR HELP

Happy new year everyone. This will be the last time I ask for support. I still need to raise £4000 to pay my hospital bill, as it's payday if there's anything you could spare and share I'd be incredibly grateful.

My recovery is getting easier with every day that passes, still some tough days, mainly when I've tried to do too much but I'm making good progress. I have my 3 month follow-up appointment with my neurologist tomorrow (snow pending!) and my first post-op MRI scan next week.

Thanks for all your messages of support, they've been so appreciated.

Take care
Anna
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Just wanted to thank everyone here. Friends and new friends. Friends of friends. All of you for your kind donations. Also to the stars who climbed Snowdon for this excellent fundraiser.

Anna had her operation in Germany on Thursday and has come to. Hopefully she will have a good strong recovery and get her life back on track. This couldn’t of happened without you. You have all helped personally save a life. I’m touched by everyone’s kindness. Lovely karma and big love goes out to you all xxxx
+ Read More
To my dear family, friends, colleagues, fellow disco dancers, red-head comrades, acquaintances and anyone that has taken the time to read this:



As many of you will know, my health has been deteriorating quite considerably for a number of years. My problems started almost 9 years ago in my early 20s when I began experiencing chronic daily nausea and dizziness. After trialling several medications and having every test available, no-one could tell me what was making me feel so sick. Years passed with me doing my best to manage this horrible condition and then 2 years ago my symptoms started to get a lot worse.



I’d always suffered from migraine since my teenage years, but the attacks were only a handful of times a year and manageable with acute migraine medication. Around 18 months ago my headaches started to increase in regularity and severity and by the end of the summer last year I was struggling with agonising headaches every single day. On top of this, I was experiencing nausea that wouldn’t respond to any kind of medication.



Then the vertigo kicked in. I’d suffered a previous episode in 2015 that had lasted for 4 months, but this time the swaying and blurred vision was so much worse and has never left me. By Christmas I was bed bound with debilitating daily migraines, nausea and vomiting, vertigo, regular loss of sight in my left eye, severe light and sound sensitivity, raging tinnitus in my ears, brain fog, forgetfulness and extreme fatigue.



I saw a neurologist early this year who diagnosed chronic migraine, migrainous vertigo and constant tinnitus. I was referred for an MRI scan of my brain as a precaution as we have a family history of brain tumours. The results showed that I have a very large, 18mm pineal cystic tumour sat on my pineal gland deep in the middle of my brain. Thankfully these types of tumour are benign, but unfortunately large, symptomatic pineal cystic tumours are very rare and are not well understood, with many medical professionals dismissing all possibility that they can cause symptoms. Many would describe them as asymptomatic and an ‘incidental finding’ despite the debilitating symptoms being exactly the same and as severe as those caused by cancerous tumours.



Hearing the word tumour, benign or otherwise, made me want to find out more and after researching these types of tumours, I stumbled across an online support group for people who had them and discovered that almost everyone had exactly the same symptoms as I was experiencing. There were literally hundreds of people in the UK alone that were battling daily debilitating headaches, visual disturbances, vertigo, memory issues, tinnitus, nausea, dizziness, seizures, sleep problems and fatigue. It was from the information in this group that I found out that there are only 6 neurosurgeons in the world who currently remove them, and sadly none of them are based in the U.K.



Undeterred I set about sending my scans to any medical professional in the UK that I found mentioned tumours of the pineal region. I must have sent emails to at least 20 consultants. A number of them came back to me wanting to help but either they weren’t the right person and would refer me to someone else or they didn’t respond.



By this point I had tried 9 different medications for migraine, as well as a 12 week trial of a new kind of treatment, the Vagal Nerve Stimulator device. I’d also paid for private Vestibular Rehabilitation Therapy to address the vertigo but this made my excruciating head pain worse. I’ve seen a nutritionist, tried acupuncture, cranial osteopathy, kinesiology and every vitamin or remedy that I found or was suggested to me that could possibly help alleviate my symptoms but nothing has worked. I am now having between 13-20 consecutive days per month of the most excruciating head pain describable. They are so bad that my partner has wanted to call an ambulance on numerous occasions as he simply hasn’t known what to do. For the rest of the days of the month my head pain is still at a 7-8/10 in severity and nothing I do does anything to take the edge off the pain or any of my other symptoms.



I cannot tell you what it feels like to experience that level of pain for an hour, let alone weeks on end with no relief. The last six months of my life have been spent pretty much confined to the four walls of my darkened bedroom. I miss working, I miss socialising and having a purpose. I don’t remember what it feels like to be well. I haven’t worked since December and am worried I will lose my job. Over the past six months I’ve missed so many important life events of loved ones such as my sister’s wedding and countless other opportunities to spend time with my nearest and dearest. Missing out on these has been heart-breaking.



I have absolutely no quality of life. At times I have completely lost my mind and have felt like giving up.



Feeling pretty desperate, I decided to send my scans to three of the six surgeons in the world that do operate on pineal cystic tumours, between them they have successfully removed over 120. All three have said that the tumour is causing compression inside my head and could very much be the cause of my problems.



I got to speak directly to one of the surgeons for over an hour when he called me to discuss my scans and was able to ask lots of questions. He reassured me that I wasn’t crazy and that he believed the cyst was most likely the cause of my problems given its size and the fact that I had tried so many medications and treatments without success. He said that that there will be no relief from medication or any treatment as essentially there is something big in my brain that shouldn’t be there, pressing on things it shouldn’t. He also said my symptoms will only get worse, and I have definitely felt this over the last few months. I have spoken to six people at length who have had their tumours removed and their symptoms have 100% improved. There are several others in the support group who have spent over $100,000 travelling abroad for the surgery, often selling property, cars, jewellery and family heirlooms to do so.



Given that I have now tried everything and the NHS are unable to help me, I am hoping to raise £35,000 to cover the cost of surgery in Germany with neurosurgeon Dr Schroeder. The money raised will cover the cost of the surgery, hospital fees, accommodation, flights and anything I may need in the 3-6 month recovery. In the unlikely event there is any left over, I will make sure it gets to a fellow ‘Cyster’ as we call ourselves, or use the money to raise awareness of this rare condition. I am also writing to my local MP to raise the profile. The support group has been a real lifeline for me and I will always be there for anyone who finds themselves with this awful rare condition in the way they have for me.



Thank you so, so much from the bottom of my heart to those who donate, many of whom I will have never met and probably never will. You will be giving me my life back and I will never be able to thank you enough for that. I understand money is tight and I often see campaigns such as these wishing I could help so if you’re reading this, please do share this page as for me it’s just as much about raising awareness as it is raising funds.

Anna xx
+ Read More
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£5,465 of £5,000 goal

Raised by 167 people in 11 months
Created August 16, 2018
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