Thursday, 27 February 2014

2013 HSP Survey Results

So, it is rare disease day again (Well, as i write, it is in India....). I am pleased to publish the results of the HSP survey which I launched in September. Many thanks are due to the 121 people who gave their time and completed the survey - this wouldnt have been possible without you.

The full set of analysis can be found here: 
https://drive.google.com/file/d/0BzEoTkR5HCWhTlFsY3k0Y1IzWlE/view?usp=share_link&resourcekey=0-43aaHBAVgWE0JxllK6FFOg

Here is a short version of the 2013 survey results....

This is a summary of the results of a survey which I launched in September 2013. There were 121 respondents who completed the survey, predominantly from the USA and the UK, but also Europe, Canada, Australia, India and South Africa.

Mobility Analysis

Answers were given by 116 respondents. Just over half of respondents use walking sticks/poles/crutches/canes and around a third of respondents use a wheelchair or mobility scooter. FES is the mobility aid used by the least number of people, with a take-up of around 5%.

Mobility Aids Used - Summary:
Respondents
Percentage
Using sticks/poles/crutches/canes
62
53%
Using Wheelchair/Mobility Scooter
40
34%
Using Orthotics/AFO
33
28%
Using Walking Frame/Rollator
31
27%
Using FES
7
6%

In the remainder of this paper whenever “sticks” are referred to as a mobility aid this term includes poles, crutches and canes. Whenever “frames” are referred to this includes both walking frames and rollators. Whenever “chairs” are referred to this includes both wheelchairs and mobility scooters. Whenever AFO is mentioned it refers to Orthotics and AFO.

The results also allow the distribution of respondents within a scale of mobility. I have devised an “HSP mobility score” which then allows me to cross-reference mobility against the other questions in the questionnaire. The definition of the HSP mobility score is;
  1. Can walk without aids but some effects
  2. Orthotics/AFO/FES and/or Sticks/Poles/Crutches/Canes some of the time
  3. Sticks/Poles/Crutches/Canes and Frame/Chair some of the time
  4. Sticks/Poles/Crutches/Canes most of the time
  5. Sticks/Poles/Crutches/Canes all of the time
  6. Rollator/Walking frame most of the time
  7. Rollator/Walking frame all of the time
  8. Wheelchair/Mobility scooter most of the time
  9. Wheelchair/Mobility scooter all of the time

Change in Mobility

One question asked people to describe how their mobility had changed over the last five years. I interpreted these results such that anyone who was either developing their first symptoms or gaining an increase in mobility score by up to around 2 was described as having a “low” change in mobility. Those who gained an increase in mobility score of around 3-4 would have a “medium” change in mobility, and those with an increase greater than around 4 would have a “high” change in mobility. 81 respondents provided enough information for me to attempt an interpretation, as shown in the following table.

5 Year Change in Mobility
Respondents
Percentage
Low
62
77%
Medium
17
21%
High
2
2%

This shows that generally changes in mobility are quite slow, with the majority (three quarters) of respondents having a low change over 5 years. There are a small number of patients, probably less than 5%, who will experience significant changes in mobility over a five year period.

Symptoms Analysis

I found 13 symptoms which occur often in descriptions of HSP and asked respondents if these symptoms were an issue for them or not. For each symptom respondents selected the most appropriate from a list of choices, which I have grouped into severity bands;
Severity
Severity Band
Do not have
-
Occasional symptom
Minor
Minor symptom
Minor
Frequent symptom
Significant, Moderate
Regular symptom
Significant, Moderate
Most of the time
Significant, Major
All of the time
Significant, Major

The following table shows the percentage of respondents with each of the symptoms, ordered by frequency – the most frequently occurring severe symptoms at the top.

Symptom
Do not have
Minor
Significant
Loss of balance
4
26
70
More stiff in the cold
4
29
67
Fatigue
8
30
62
Bladder problems
18
39
43
Stress
19
42
39
Back pain
22
42
36
Clonus (jumping feet)
30
37
34
Numbness
31
36
33
Depression
34
34
32
Bowel problems
39
36
25
Loss of vibration sensitivity in legs
39
37
24
Pes cavus
48
15
38
Hammer toes
53
18
28

This shows that the two symptoms which affect people the most are loss of balance and getting more stiff when it is cold, which is a significant issue for 70% of respondents, and an issue for more than 95% of respondents. Fatigue affects more than 90% of respondents and is a significant issue for more than 60%.

Bladder problems, stress and back pain affect around 80% of respondents, significantly in about half of those. Clonus, numbness and depression affect around 70% of respondents, and show a similar pattern where half of those affected are significantly so.

Bowel problems and loss of vibration sensitivity affect around 60% of respondents. These symptoms appear to be significant for a smaller proportion of respondents. Pes cavus and hammer toes affect the smallest proportion of respondents, around 50%, and these symptoms appear to be significant for a greater proportion of respondents.

Symptoms - Analysis of Symptoms against Mobility

For a more detailed analysis I grouped the respondents into groups according to mobility;

Number of Symptoms – walking unaided

Those who can walk unaided tend to have 4-5 minor symptoms, up to three moderate symptoms and no major symptoms. All respondents in this group had at least three symptoms, at least two of which were minor.

Minor symptoms are likely to include Loss of Balance, Stiffness in the Cold and Fatigue, and may include Bladder problems, Stress, Back Pain, Clonus, Numbness or Bowel problems. Moderate or major problems may include Stiffness in the Cold, Fatigue, Stress, Back Pain, Clonus or Numbness.

Number of Symptoms – use aids some of the time

Those who use mobility aids some of the time tend to have 4-5 minor symptoms, up to three moderate symptoms and up to one major symptom. All of the respondents in this group had at least five symptoms, at least one of which was minor.

Minor symptoms are likely to include Loss of Balance, Stiffness in the Cold and Fatigue, and may include Bladder problems, Stress, Back Pain, Clonus, Numbness or Bowel problems. Moderate or major problems may include Stiffness in the Cold, Fatigue, Stress, Back Pain, Clonus or Numbness.

Number of Symptoms – using mobility aids all or most of the time

Those who use mobility aids all or most of the time tend to have 2-5 minor symptoms, up to 5 moderate symptoms and up to 5 major symptoms. All of the respondents in this group had at least 7 symptoms.

Minor symptoms may include Bladder problems, Stress, Back Pain, Clonus, Numbness, Depression, Bowel Problems and loss of vibration sensitivity in the legs. Moderate or major problems may include Loss of Balance, Stiffness in the Cold, Bladder problems, Stress, Depression, Bowel Problems, Pes Cavus or Hammer Toes.

Mis-diagnoses

One question asked people what they had been diagnosed with before getting their HSP diagnosis. 100 respondents answered this question. 20 respondents indicated that they had been correctly diagnosed with HSP the first time.

The 80 respondents who had been mis-diagnosed gave in total 126 different misdiagnoses. Some respondents listed just one misdiagnosis, whereas others listed a great many. In total there were 59 different conditions listed. Twelve of these were given at least three times accounting for nearly 60% of mis-diagnoses, as shown in the following table;

Mis-diagnosis
Number of diagnoses
Multiple Sclerosis (MS)
19
Cerebral Palsy
12
Arthritis
6
Charcot-Marie-Tooth disease (CMT)
6
Neuropathy
5
Ataxia
4
Motor Neurone disease - Primary Lateral Sclerosis (PLS)
4
Cerebral Palsy - Spastic Diplegia
4
Muscular Dystrophy (MD)
3
Motor Neurone disease - Amyotrophic Lateral Sclerosis (ALS)
3
Peripheral Neuropathy
3
Spinocerebellar Ataxia
3

Like this? in other years:
Overview of all my surveys: http://hspjourney.blogspot.co.uk/p/my-on-line-resarch.html
2016: Fatigue, bladder, bowel & information: http://hspjourney.blogspot.co.uk/2017/02/2016-survey-results.html
2015: Modifications at home, depression, quality of life: http://hspjourney.blogspot.co.uk/2016/02/2015-survey-results.html
2014: Medication, exercise & relaxation: http://hspjourney.blogspot.co.uk/2015/02/2014-survey-results.html

Monday, 10 February 2014

New large HSP research study reported

A new study about HSP has just been reported. The study took about 10 years to complete, and has examined the genes of about 100 HSP patients, focussing on countries where HSP is found but genetic studies are rare. This includes Egypt, Pakistan and Iran. Part of the study identified 18 new genes for HSP.

But, with all this data they were able to look at the wider picture, and made links between HSP and other more common neurodegenerative disorders, such as Alzheimer’s disease, Parkinson's and amyotrophic lateral sclerosis (ALS).This suggests that these conditions may have some common ground, and that drugs which target these overlapping genes could help to treat more than one disease. 

They were able to create a plausible network of proteins involved in this disease. Of the 18 new genes, 15 were identified from the genetic tests but 3 were from looking at this network. They call the network the "HSPome". Here's an extract;



This work has identified several promising targets for development of new treatments.

Readers should note that I have not seen the article, and my notes are based on what others have said about it.

Links to various reports on the study;
http://phenomena.nationalgeographic.com/2014/01/30/now-this-is-how-you-find-disease-genes/
http://sciencedigg.blogspot.co.uk/2014/02/a-unified-process-for-neurological.html
http://www.newswise.com/articles/scientists-discover-new-genetic-forms-of-neurodegeneration
http://spatax.wordpress.com/2disease, P09/contribution-of-the-spatax-network-to-the-identification-of-18-new-causative-genes/

And, a link to the article itself;
http://m.sciencemag.org/content/343/6170/506
http://dx.doi.org/10.1126/science.1247363

Reference: Novarino, Fenstermaker, Zaki  Hofree, Silhavy, Heiberg, Abdellateef, Rosti, Scott, Mansour, Masri, Kayserili, Al-Aama, Abdel-Salam, Karminejad, Kara, Kara, Bozorgmehri, Ben-Omran, Mojahedi, Gamal El Din Mahmoud, Bouslam, Bouhouche, Benomar, Hanein, Raymond, Forlani, Mascaro, Selim, Shehata, Al-Allawi, Bindu, Azam, Gunel, Caglayan, Bilguvar, Tolun, Issa, Schroth, Spencer, Rosti, Akizu, Vaux, Johansen, Koh, Megahed, Durr, Brice, Stevanin, Gabriel, Ideker, and Gleeson. 2013. Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders. Science. 

Monday, 27 January 2014

A trip to the doctor

This year is a year of action. So, to this end I've been to see my doctor (GP). We talked about three things.

Firstly, I've asked for a referral to the National Hospital so that I can talk about rates of progression, future medication and get some advice on stretches, exercises etc. I'll let you know what happens.

Secondly, I mentioned my recent bowel and bladder issues. We managed to rule out infection, prostate and muscle issues, leaving most likely to be an HSP symptom. I'll have another appointment about this.

Thirdly, we discussed my low mood of recent times. I've a number for a local NHS support service. I called and need to make an appointment here too.

So, in summary, not very interesting, but its my first experience of these, and I thought useful to note the process.

In other news, my first column appeared in the UK HSP support group newsletter today. Its based on my post some months ago on the paper about bladder issues in HSP patients.

Also, now we're into 2014 it's time to start analysing my survey results. I had about 120 responses, so that's brilliant. Thanks to everyone we who answered. Some interesting answers on the misdiagnosis question. I'm aiming to report on rare disease day (28th Feb).

Thursday, 9 January 2014

Rare disease patients outnumber cancer patients

I saw this blog post on the Nord website: http://blog.rarediseases.org/the-solution-to-diagnostic-delay-may-be-closer-than-we-think/ which has an interesting point of view. I was a little surprised to find that rare disease patients outnumber cancer patients by about two to one. (this is a US number, and the comparisons in the blog post relate to the US cancer/rare disease population).

The stats for cancer in the US are here: http://www.cancer.org/cancer/cancerbasics/cancer-prevalence, with various stats for rare diseases on the Nord blog. I suppose that this arises because this is a comparison with~7000 rare diseases and ~200 cancers.

I like the point of view presented here - essentially that doctors ought to be more aware of the potential for rare diseases, but I can also see the other side - to me it makes more sense for doctors to know the more common stuff inside out.

Saturday, 28 December 2013

Review of 2013

Another year has passed and its time to reflect on things and consider how different things have become over the year.

Knowledge
This has been a bit of a mixed year on the knowledge front. I had spotted that some of the most frequently viewed posts related to HSP symptoms, and I've done some investigation here. I also met with Evan Reid and went to the HSP support group AGM getting lots of information there, and also various new connections made with lots of avenues to explore. I've not been looking too much at the PubMed database this year. Perhaps I'll chalk 2013 up as a connections year rather than a knowledge year.

Symptoms
Looking back at my 'symptoms update' posts I can see this year has been mainly about getting more stiff and finding certain things more difficult to do than before. I also have been spotting some issues on the bowel/bladder front. I speculated that this might be the start of bigger/quicker changes.

This Blog
I 'came out' on rare disease day (Feb 28) and joined up my various on-line presences. I've been more active in talking about what I have been blogging about, and indeed more people are reading this. Thanks!

Authoring
Following my posts on the UK HSP Support Group AGM I've been asked to regularly write for the newsletter, which is an honour to do.

Survey
I also launched my first on-line survey, which has had many (over 120) responses, and I'm looking forward to analysing the responses early in 2014. The survey will be back in the Autumn.

Other things like the filming project and the gradual expansion of pages on the blog have taken a bit of a back seat in the year partly as a consequence of this, and partly due to being busy with my young family and busy at work.




Monday, 16 December 2013

Another outlet for my messàge, communities update

The other week I met up with Ian Bennett of the UK HSP support group. Ian has asked me to write a regular feature in the newsletter, covering the medical side of things. I was pleased to accept. Effectively, this will partly be a re-write of some of the things I have already written, and mostly a write of things I haven't yet found!

Towards the end of November I signed up for the patientslikeme website. I quite like the tracking tools they give you. I had been trying to find an app to allow me to track these things, but that didn't seem to be too easy to find. The patientslikeme site let's you track some of the relevant symptoms, grouping into mental, physical and social - which draws some parallels with the presentations from the AGM. I'll keep updating my details, and give feedback. My immediate grumble is that I don't seem to be able to update my details from my tablet.


Wednesday, 20 November 2013

Symptoms update - illness & tiredness

Ok. I posted a few months ago that I wondered if I was starting to get more signs of HSP. This has been a little bit more and more since then. At the weekend I was sick - probably a food bug, but that's not important. My youngest son was sick Fri/Sat, with my eldest son and me both being sick Sun night, presumably the same thing. Needless to say it was quite a sleepless night on Sunday. I could really tell that I was exhausted Monday morning, and it felt so difficult even to stand up. I felt like I had no energy and I had to really think about trying to stand up.

Some time ago I had observed about things being worse when I was tired, and I suspect that this combined with sickness just emphasised the effect. Monday night was a good nights sleep, and I was back to normal today.

I read, via twitter, the spoon theory a few months ago, and I saw that this seemed a very good way of explaining a long term chronic health condition. I have a feeling that HSP is going to need this explanation. If you've not seen the theory before have a read: http://www.butyoudontlooksick.com/wpress/articles/written-by-christine/the-spoon-theory/ 

This is probably also the place to note that in addition to noting some 'issues' with my legs (which I'm perfectly happy to talk about) I've also been spotting some urinary and bowel issues (which I'm not so comfortable sharing). I've been having some urgency 'issues' recently with some 'events' being a little too close for comfort. For completeness, I'll also note that I've spotted at some time most of the effects noted in my post about a year ago. It's a good job I don't need to worry about how many times I flush!

Wednesday, 6 November 2013

Overall Update

I realised the other week that it had been a while since I updated the index for this blog, so I've added the last 12 months of posts to the index such that it is now up to date. Perhaps this becomes an annual job as its about a year since I put the index up in the first place.

I've also added some technology to the blog. I was looking at someone elses Blogger Blog and they had various features that I wanted. I had a bit of an explore and managed to find a search feature, and e-mail/RSS subscriptions. So. those are to the left of this and you are welcome to use them if that helps you keep in touch.

In recent correspondence I've also become aware of three more HSP groups - Finland: http://www.ms-liitto.fi/hsp, Austria: http://www.salzburg.at/miniweb/sspshg/ and Europe: https://sites.google.com/site/eurohsp/home. I wonder if there are any more?

I've also been looking into the SPATAX network: http://spatax.wordpress.com/ and observing that many of the researchers here are those with the most papers in my trawl of papers.

Finally, I've over 100 completed reponses to my survey so far, so many thanks to those that have completed it. I'm still trying to promote this around HSP groups, so I dont think I'll look at results until later in the year.

Tuesday, 15 October 2013

UK flu vaccination

I got a letter from my doctor the other day saying I was entitled to a vaccination against flu/influenza. I was a little surprised as I thought I would be the least likely person in my home.

However, according to the NHS website people with neurological conditions are entitled to this http://www.nhs.uk/Conditions/vaccinations/Pages/who-should-have-flu-vaccine.aspx. Now, I'm not sure my HSP is 'chronic' but at least it explains the letter.

I spotted this on one of the Facebook groups.

Sunday, 13 October 2013

Groups around the world

I posted (about 3 years ago) a list of support groups that I'd found which had websites in English. In the interests of letting more people know about this blog and trying to get some more reponses to my survey I've made contact with all of the HSP groups I can find (thanks to lists on the UK HSP group and Rare Connect). The full list (in no particular order) is:

UK: http://www.hspgroup.org/
US: http://www.sp-foundation.org/
Australia: http://www.hspersunite.org.au/
Switzerland: http://www.hsp-selbsthilfegruppe.ch/index2.php
Spain: http://www.aepef.org/
France: http://asso.orpha.net/ASL/index.htm
Germany: http://www.hsp-verein.de/startseite.html
Germany: http://www.hsp-info.de/ (Tom Wahlig Foundation - a group who funds HSP research projects)
Norway: http://www.regioner.nhf.no/index.asp?id=63230
Italy: http://www.vipsonlus.it/
Denmark: http://www.sca-hsp.dk/index.html
The Netherlands: http://www.vsn.nl/ (neuromuscular disease group)

These groups are all in Europe, North America and Australia, and this grouping of countries therefore provides some support for HSP sufferers covering about 15% of the worlds population, so I'm wondering how people with HSP in the other 85% of the world get their support. (I accept I've made a number of gross simplifications here).

If any readers know of support groups/communities/websites for HSP in other parts of the world, I'd love to hear from you.