Chronic Kidney Disease in found more in women 14%, than men 12%

Many of us are what you would call normal, got a good healthy weight.. eat healthy, have very busy lives, carrying on normal daily routines of work, picking up groceries, doing laundry and just living then Boom…when we attend our GP, end up at Accident and Emergency we are told that our Kidney are not fully functioning as it should be.

Many people with chronic kidney disease (CKD) will not have symptoms because it does not usually cause problems until it reaches an advanced stage.

Early stage of CKD is not normally picked up unless blood tests are done routinely and it may be been prevented or slowed done, medicine and regular tests to monitor it may help stop it becoming more advanced.

Later Symptoms can include:

1. weight loss and poor appetite

2. swollen ankles, feet or hands – as a result of water retention (oedema)

3. shortness of breath

4. tiredness

5. blood in your pee (urine)

6. an increased need to pee – particularly at night

7. difficulty sleeping (insomnia)

8. itchy skin

9. muscle cramps

10. feeling sick

11. headaches

12. erectile dysfunction in men

In many cases, CKD is only found when a routine blood or urine test you have for another problem shows that your kidneys may not be working normally.

A few things to look out for, if you have persistent symptoms of CKD, such as:

weight loss or poor appetite

swollen ankles, feet or hands

shortness of breath

tiredness

blood in your pee (urine)

peeing more than usual, particularly at night

Your GP can look for other possible causes and arrange tests if necessary.

Regular testing is recommended if you have:

high blood pressure

diabetes

acute kidney injury – sudden damage to the kidneys that causes them to stop working properly

cardiovascular disease – conditions that affect the heart, arteries and veins, such as coronary heart disease or heart failure

other conditions that can affect the kidneys – such as kidney stones, an enlarged prostate or lupus a

family history of advanced CKD or an inherited kidney disease

protein or blood in your urine where there’s no known cause

You’re also more likely to develop kidney disease if you’re black or of south Asian origin.

I am not saying that other races do not get it but it really in the minority backgrounds

My diagnoses was identified by having fluid present in my abdomen whilst at work when I was 26 years old. I was stage 2 with Kidney disease with as well as one of CKD’s most common but severe complications, anaemia.

14 years after the initial diagnosis, I progressed to end-stage renal failure where the only treatment at the time was a transplant.

I was offered a transplant from my lovely husband “I was really shocked as I didn’t feel that I was there yet. The transplant failed in 2007 soon after surgery, I have been on haemodialysis and is now a home patient utilising nocturnal dialysis as my treatment of care.

So the purpose of setting up this business is because during the last 10 years of being on dialysis and going on holiday with a mobility issue I have experienced a few things.

My Trust changed the way we book holidays, we used to have a coordinator that did all the holiday bookings,

Then we were told that we need to do our own holiday bookings and the nurse will complete the form and give you a copy and send the form across and everything else is left up to you

Sometimes it can be quite stressful because you have to contact the Dialysis unit first and then find your holiday your flights and your transfers.

I have used other agencies and they that found the booking dialysis unit and was difficult and it took forever and when they found the unit.

I no longer had the holiday booking, therefore I no longer needed to attend the dialysis unit or even book the holiday

because it no longer met my need. Because of these experiences and speaking to others, I thought I want to help to take the strain and stress from kidney and mobility patients/clients and handle the complete process and more.

I love travelling and encourage all Kidney patients to travel.

Have you ever been to Aberdeen? What do you know about Aberdeen. The name given to Aberdeen translates as ‘mouth of the river Don’, and is recorded as Aberdon in 1172 and Aberden in c. 1180. It is the third largest city in Scotland. Aberdeen is historically known for its strong ties with the North Sea.

Boasting notable fishing and shipping industries as well as a lively cultural scene. Aberdeenshire stretches from “one of the last great places on earth” (the Cairngorms) to “one of the world’s top-rated coastlines”. So says National Geographic. And The Scotsman (one of Scotland’s national newspapers) calls its city of Aberdeen – where ships dock right up against the city-centre streets and dolphins leap in the busy North Sea harbour – “one of the most architecturally distinctive in Europe”.

It is a compact city with wide open spaces; walk along a mile long stretch of golden beach (you may even spot dolphins playing in the harbour mouth) and admire the sparkling granite architecture that we are so famous for. Step back in time in Aberdeen’s old town as you visit the cobbled roads and historic buildings in Old Aberdeen, or stay in the heart of a bustling city with a vibrant foodie scene – including big names like Mackie’s and BrewDog.

Perhaps it’s somewhere to visit here in the UK this year.

I too am kidney dialysis and mobility person, I know how stressful it is to book a holiday, using the high street and not getting a personal service.

I’ve been there and that is why I want you to have a stress free holiday,

Listen if you are tired of using the high street to book your holiday, I will take all the worry away from you, I will take care of all the arrangements, l will create and make the holiday of your dreams.

WHAT IS CKD

Chronic Kidney Disease in found more in women 14%, than men 12%

Many of us are what you would call normal, Boom…when we attend the GP, end up at A&E we are told that our Kidneys are not fully functioning as it should be.

Many people with CKD will not have symptoms because it does not usually cause problems until it reaches an advanced stage.

Early stage of #CKD is not normally picked up unless blood tests are done and it may be been prevented or slowed done, medicine and regular tests to monitor it may help stop it becoming more advanced.

Later Symptoms can include:

1. weight loss and poor appetite

2. swollen ankles, feet or hands – as a result of water retention (oedema)

3. shortness of breath

4. tiredness

5. blood in your pee (urine)

6. an increased need to pee – particularly at night

7. difficulty sleeping (insomnia)

8. itchy skin

9. muscle cramps

10. feeling sick

11. headaches

12. erectile dysfunction in men

In many cases, CKD is only found when a routine blood or urine test

A few things to look out for, if you have persistent symptoms of CKD, such as:

• weight loss or poor appetite

• swollen ankles, feet or hands

• shortness of breath

• tiredness

• blood in your pee (urine)

• peeing more than usual, particularly at night

Regular testing is recommended if you have:

• high blood pressure

• diabetes

• a family history of advanced CKD or an inherited kidney disease

• protein or blood in your urine where there’s no known cause

You’re also more likely to develop kidney disease if you’re black or of south Asian origin.

I am not saying that other races do not get it but its really in the minority backgrounds

My diagnoses was identified by having fluid present in my abdomen whilst at work, I was 26 years old. I was stage 2 with Kidney disease as well as one of CKD’s most common but severe complications, anaemia.

14 years after the initial diagnosis, I progressed to end-stage renal failure where the only treatment at the time was a transplant.

I was really shocked as I didn’t feel that I was there yet. The transplant failed in 2007 soon after surgery, I have been on haemodialysis and now a home patient utilising nocturnal dialysis as my treatment of care.

During the last 10 years of being on dialysis and going on #holiday with a #mobility issue I have experienced a few things.

My Trust changed the way we book holidays, we need to do our own holiday bookings and the nurse will complete the blood forms etc,

It can be quite stressful, you have to find hotel, flight and transfers.

I have used other agencies and they find the #dialysis unit and it was difficult and it took forever.

I lost the holiday booking.

Because of these experiences and speaking to others, I want to help to take the strain and stress from kidney and mobility patients/clients and handle the complete process and more.