Life-Changing Report – What you need to know to get it right… and get your life back.

Systemic Lupus Symptoms In Women – Systemic Lupus Erythematosus or SLE

Faye’s Living With Lupus Report – Long-Time Lupus Sufferer.

What You Need To Know
To Get It All Right The First Time
+++ “I got it all wrong, but you don’t have to” +++

Lupus Symptoms In Women

Faye - Lupus Symptoms In Women

Hi! my name is Faye Cooper and for over 25 years my family and I have been living with the highs and lows of my Lupus Symptoms In Women.

(Looking back, I now realise that actually I had my first Lupus Symptoms before I was 15 years old)… If only I’d had this information, which has taken me years to find out and collect – I would not have had to endure all those needless years of distress and suffering.

When I was first diagnosed with Lupus, it never occurred to me that my family and friends would have to live with my illness as well.

I thought it would just be a matter of taking medication and getting on with a normal life.  How wrong I was – This chronic illness does not just affect the sufferer, it has a profound effect on family and friends as well.
 
 

I Got It All Wrong With My Children
I wish I had known how to see things from their perspective as well

One of the main things that struck me was that I hadn’t realised that my children were growing up and had become more aware of the fact that I was ill.  They were worrying about all sorts of things that COULD, (and should), have been discussed and explained.
 
While writing this book it became quite clear to me that
Lupus was not just about me being ill…

…it’s also about dealing with it as a family. At this point I asked my eldest daughter to write and explain what it is like to live with a mum who has Lupus.
 
I knew Alex wanted to go to university, but I was not aware that she wanted to escape from the situation at home.  What I had expected her to write about was that her mum is always tired and never has the energy to enjoy life with her.

During the final stages of putting the book together, my second daughter Megan decided she would have a read.  After reading it she insisted on adding her point of view.

Although I had realised that my illness was affecting her, I hadn’t expected such honesty, so much so that it made me cry. Anyone who knows Megan will tell you that it is written straight from the heart and explains much of the way she has acted over the last few years, especially at school.

My two younger children have yet to tell me how Lupus has affected them -
I will definitely be talking to them and reassuring them in the future.

 
 

I Got It All Wrong With My Family & Friends
They didn’t know my situation, so they didn’t know I needed help!

Getting The Support of family & friends can be very difficult…
Telling people that you are not well or exhausted only puts up barriers.  It is so easy for family and friends to expect unrealistic goals from you and for them to begin to think that you are either playing on the illness or just being downright lazy.

The information in this book can change your life. Just getting the people around you to read it will change their whole concept of what you are going through.
You will have a stress-free way of getting them on side…

The others reading the book will lighten your load.
This on its own makes it Indispensible!

 
 

I Got It All Wrong With The Doctors
When seeing my Doctor – I wish I had known what to expect.

Had I known what to do, say and expect in the first place would have saved me from a lot of grief & suffering over the years.

 
Know Your Symptoms…

Some of the first things you may notice other than the relentless exhaustion, hot, stiff & swollen fingers and feet, are the loss of appetite and feeling sick.

Secondary problems can occur, such as dry eyes & mouth and dry skin.
Thyroid problems can cause the body to slow down, causing constipation and lethargy, or speed up causing hyperactivity and diarrhoea…

Keeping a record of how you are feeling, and what
may have caused any ups & downs…
Is Essential In Optimising Your Treatment.

 
Know The Questions…

First you need to find out if you have Lupus.  Has your Doctor done all the obvious tests for problems like Lethargy, Exhaustion, Loss Of Appetite, Feeling Sick, Hair Loss?
If all of these are inconclusive, then you need to ask for blood tests relating to Rheumatology.

When you’ve read my ebook you will know how to approach your own Doctor and also know what kind of specialist should be treating you…

…getting This Right Will Get You TO THE RIGHT PEOPLE More Quickly.

 
 

I Got It All Wrong Most Days
I ran out of energy at all the wrong times.

Know How To…

Cope with exhaustion by learning how to pace yourself.
Learn how to arrange your days in order to cope.

You will get valuable information from the ebook that will help you every day,
and so get you a better Quality-Of-Life

 


You Don’t Have To Get It All Wrong Like I Did
There are important things that both you AND the people
around you have to know… and it’s in the book.


Just by reading this book…

  • You Get… To Get The Support of family and friends.
    By having THEM read "My Lupus Treadmill", they will understand what you, and other Lupus victims, have to put up with every day.
     
  • You Get…To Know Your Symptoms by keeping a record or diary of all your symptoms and taking photographs of rashes and swellings to show your doctor.
     
  • You Get… To Know The Questions you should be asking  your Rheumatologist.
     
  • You Get… To Know How to cope with your relentless exhaustion.

You Get all this by reading my Living With Lupus eBook "My Lupus Treadmill"  –  Faye Cooper.


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 *** 

Improve your quality-of-life…
…At just $9.97, all those who most need this life-changing information will be able to get it & benefit from it.

 

Get The Benefits Now
Immediate Down-Load

Get All The Benefits that my eBook can provide.
           ”Life Changing” information.
…I know this information will be well worth it for you, as it has been for me – Faye Cooper.
 


Beat Lupus and Get Your Life Back


 

  • How To Get Family Support…
  • How To Record Your Symptoms…
  • What Questions To Ask…
  • And How To Cope…


 Just Read My Book.

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Real Practical Help giving you a better life…
     ( For less than the cost of a box of preservative-free eye drops )

And You Just Can’t Lose – because all the risk is on me.
You have my 60 day “Full Money Back” Guarantee

 
If you don’t find that the Life-Changing Information in my living with lupus eBook makes a real difference to your quality-of-life, and helps you and your family & friends, then simply ask me for a refund -You keep the book as I am sure if you take the time to go through it again it will help you… Faye Cooper.

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