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Emma Parslow Fibromyaligia Fund

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 Hi my name is Emma Parslow Cope I’ve started a GoFundMe campaign, and it would mean a lot to me if you could support the campaign by making a donation or sharing my campaign with your friends. You can see the campaign link here: [https://www.gofundme.com/EPC-Medical-Fund]. 

My life will change forever, with just a click of a button and with a small donation my dream of being a normal person will come true. I would appreciate it so much if you could read my story. Xxx

I was diagnosed on the 3rd October 2016 and have suffered with this condition for seven years. The cause of Fibromaglia was due to a football injury in 2010 after a traumatic fall on pitch, which damaged my hip and my lower back that has deteriorated over time. I feel that I have no life and that I am living in a woman’s only prison which I am in stuck in black hole, crying out for help.

This is taking over my whole life and was very close on New Year’s Eve to taking an over dose of pills due to what the condition is doing to me. Doctors, Hospital pain clinic say they don’t know how to deal with me and I feel like I am deteriorating day by day.

My family can no longer support me financially and they have all had enough. This has caused no end of upsets with all my relatives, due to the lack of understanding which is not my family fault.

I feel that this is my only hope for keeping me alive, but I can’t do it on my own as I need financial help from my country. I have never had to ask for anything like this before, but I am in desperate need.

I have made my own programs since leaving my work place last August and have graphs for evidence on how hard I have worked to try and get an answer, as to why I am so poorly. You can all then see how much time I have put into getting myself right without the help of the NHS because they are unaware of my condition and dont no anything about Fibro.

I have now come to calling out for my country to support me and donate anything you can as I have caulcualted that I will need up to £10,000. Any donations will be gratefully appreciated as I now know how important it is to live my life.

I believe I am born to work and make a huge difference to people lives, but I can’t do this without the help and support from you all. If my dream comes true and I can get the donations required I will promise I will help others that are in need. I will give 100% and more in the future and will keep you all updated on my progress throughout.

I am 27 years old with a passion and love to succeed through life. I resigned from my post in August 2017 because I could no longer function due to my physical and mental condition

The Centre Parcs Cycle Centre was my everything as I loved the guest care so much that I gave my all to the role. The best bit of my job was seeing the joy and smile on the guests faces and having the ability to make there holiday dreams come true, which was best feeling you could wish for. I shall attach one of my guest nomination on this site, so you can have a read.

My condition is stopping me work, have social interaction playing with adopted Nieces and Nephew's. I can’t even sit and chat to someone for to long because I am unable to concentrate on what they are saying as I get to exhausted, so I have to go home to bed. I sometimes have to walk away from the situation that is very upsetting and hurtful for others. I have been on so many medications and none of them appear to be working even the antidepressants are not helping me.

My family can no longer do anything for me, so I would really appreciate your help. I never realised you could setup a fund like this that could change my whole life. I have not been Emma Parslow Cope for a long time now so I would like to get the old Emma back, which would be amazing.

My symptoms i get:

1. Fatigue 
2. Exhaustion 
3. Painful joints muscles  
4.burning pain continuous through out whole body.
5.painful wrist and ankles
6. Swelling up of muscles increased inflammation stops me from wearing certain clothes 
7.sevier headaches 
8. Flares ups that cause flu type symptoms temperature high. All body gets tightened feel strangled 
9.throat tightens 
10 knives scissor pains in overies that leads to being bed bound and can not walk 
11. Anxiety disorders : can’t plan anything,  very scared all the time, get very sharp agitated quickly, not able to comprehend and taking things in, memmory impairment. Fibro fog is loss memmory. I need someone always to be with in mental health appointments 
12, Depression, angry and very low self asteem, the more the exhaustion than the more pain I get which leads to deep upsetting depression state that leads to calling crisis team. 

My goal in life is to really make a difference to others. You would make a young girl extremely happy and change my life forever. I hope I can live a normal proactive life and smile every day so I can be grateful to my life.

I will thank you all from the bottom of my heart who have changed my life forever. I will make a promise that I will strive to do my best to help change other people lives after I am given the oppertuinty to go to the Fibro Clinic in London for specialist treatments.

Thank You very much for taking the time to read this and I hope you can donate. Anything you feel comfortable would be much appreciated. I hope that in the future that I can make a huge difference in the world.

Fibromayglia Clinic, London
9 Harley St Marylebone, London W1G 9QY

Treatments:

1. £215 to get all labortory tests done
2. £29 for all bloods to be processed
3.£75 to get the treatment done at the clinic
4. 5x £160 phone calls
5. 5x £175 in prescription costs.
6. 5x £175 Botox (if required)
7. £25 Prescription Fee
8. £300 for Consultation
9. £300 for MRI
10. £300 X-Rays
11. 3x £285 Continuing Treament
12. £160 telephone appointment continuing treatment.

Other expenses including petrol, bus fares, over night accommodation if required for me and one other, £1,000

Any outstanding funds will be dionated to Fibromaglia UK charity to help others in my situation.

Also my Twin sister Louise Parslow Cope that has Stage 2 Fibromaglia I would like to get my twin sister looked at is well before she gets bad like me. All it takes is a click of a finger and your life gone completely. 

So so please great Britian get behind me so I can make my dream come true, let me live a normal proactive life. How great would it be to help my twin sister out and the first person I can help once back on my feet. Than will help as many other people through my lifetime. 

My twin sister Louise Parslow Cope has been through thick and thin with me believed me when no one else did, diagnosed me before doctor did. So to give my sister some help to would be amazing. 

Please get behind my campaign not only changing one life but two lives through your love and surpport. 

Emma Parslow Cope

Organizer

Emma Parslow Cope
Organizer

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