About me section


Hi, my name is Paul, I’m 26 and I have CIDP (Chronic Inflammatory Demylinating Polyneuropathy). This blog will try to document my symptoms, progression and treatment from start to finish, along with my frequent encounters with the NHS in both West Yorkshire and south Wales. This blog is an attempt to keep you and more importantly me entertained on this ongoing, ruddy bumpy, uncomfortable and often frustrating journey.

 photo me_mid_3_peaks-1.jpg

This is me. Mid way through the Yorkshire 3 peaks in July 2012. 13 miles down, 13 more to go! (Not at all demoralised)

I can honestly say, my feet have never ached so much in my entire life! But from this I hope you can tell I was just like everyone else; reasonably fit, happy, quite outdoorsy and a keen angler (A link to my other blog Paul on Coarse Fishing can be found here). Now, I’m considerably less fit, still happy (with a few moody bouts), generally house bound (unless I break the Zimmer out) and it’s been well over a year since I’ve wet a line. If you’ve read this far you’re probably either aware of what CIDP is or are thinking “what on earth is this guy on about?” If either of those are the case, you’re committed, and I’m about to begin the story from the beginning...

Showing posts with label Tests. Show all posts
Showing posts with label Tests. Show all posts

22 July 2013

Meeting with Debbie

It was time for me to make another appointment with Robin Lane Surgery. Prise aside, I never take time off work. If I’m ill, I’m ill, nothing that a Lemsip won’t sort. And if that fails there’s always solphadol! The prospect of taking an extended period of time off to get well never occurred to me, as I was prepared to soldier on.


Neurology appointment 1

Neurology Out-Patients is in the Jubilee Building of Leeds General Infirmary and is a surprising distance when reduced to baby steps. Still, I was optimistic, that with 2 appointments on one day I was going to finally crack this nut and get some answers. Dutifully, my partner and I set out and extensive timeline of symptoms, falls and aches as mentioned in my previous post (thanks Rach), which I was prepared to recite to both consultants if required. Arriving at the Neurology and Cardiac desk I took a seat and waiting to be seen by Dr. Dunn.


8 July 2013

Abnormal... Great

10 days and several chasing phone calls passed between having my nerve conduction tests and finally receiving a phone call confirming my NCS results had been received. The results were “Abnormal throughout”. Abnormal how, they couldn’t tell me, but further tests would be required. Great. Being told this information via a doctor at Robin Lane Surgery was frustrating (although not in any way the GP’s fault), as they are GP’s and not specialists they couldn’t answer my questions about what these results meant or what could be causing the abnormalities.

2 July 2013

Nerve Conduction Study 1 – Plug me in and turn me on!

The day had finally arrived when I would be having my nerve tests! My symptoms had reached what I thought was a plateau, and despite my drugs best efforts I arrived at the Brotherton Wing of the Leeds General Infirmary (LGI) having fully Googled what an NCS can and can’t diagnose, and again ALS reared its ugly head in my conscious.

21 June 2013

Bloody bloody bloods

A few days after my appointment with Dr Hambridge I had my blood taken, and as the title of this post suggests, they took a lot! But as I was surprised to discover, there are a whole raft of other potential ailments and illnesses that present with a tingling sensation in the extremities. Not particularly encouraging, (especially as the on-going joke between me and my partner was that “I never get ill”) but I wanted answers!

I hate needles...

20 June 2013

The Beginning


The end of December 2012 saw the onset of my initial symptoms, which began with a very faint numbness in my fingers. Not a pins and needles sensation but a buzzing feeling in each of my fingers, as well as a progressive weakness with my grip, but fortunately no sensory loss. I didn’t think anything of it for some time...