HMSA Giving GPs the Tools

http://uk.virginmoneygiving.com/fund/HMSAGPTools

Total raised

£1,897.52

Total raised (+ Gift Aid)

£2,093.77

Offline total

£280.00

 Parent with child in lap consults a GP        

The HMSA's 'Giving GPs the Tools' Campaign!

We know from anecdotal reporting and snapshot surveys, that it takes 55% of our people over ten years to gain a correct diagnosis of hypermobility spectrum disorder, previously joint hypermobility syndrome, or hypermobile Ehlers-Danlos syndrome. It is probable that a similar outcome may be seen in the other conditions we support; all Ehlers-Danlos syndromes, Osteogenesis Imperfecta, PXE, Stickler syndrome, Marfan syndrome etc.

                     (How long did it take me? I was diagnosed ar 54. I had pain

                      all my life but I have only just been told what was wrong

                                                     with me.)

This 10 year journey sees our members feeling dismissed by medical professionals, who have no understanding or little knowledge, of what can often be complex and multi-systemic conditions. There is little training for medical students on the subject and post qualification training may not cover heritable disorders of connective tissue or hypermobility spectrum disorders.

                       (No-one believed me. They said it was all in my head! But

                        I knew it isn’t normal to have pain all the time! I feel so

                                                    angry…)

           Unhappy child is consoled by a parent

                      (Getting a diagnosis just shouldn’t be this hard!)

Yet we know that delays in diagnosis are costly. It can lead to a negative impact on education, employment, family and friend relationships, and increases potential for disability and distress. It can cause disruption not just for the individual but to all their loved ones; physically, emotionally, socially and economically.  

The vast majority of hypermobility spectrum disorders can be, and should be, diagnosed by a GP. The diagnosis is not necessarily a complicated one but too often GPs don’t know how to diagnose or that such a diagnosis exists. 

         (I have a diagnosis! I am so relieved! I feel believed. All I am doing

                                          is sitting here crying.)

And once they make that diagnosis, they often do not know how to, or where to, start in the management of the varied systemic issues that our members can face. The HMSA is here to support this process by providing information and resources to all types of professionals, especially GPs and their patients.

doctor prepares to test a child's reflexes

                  (I have my diagnosis. Now what do I do? Who do I see?)

Getting a diagnosis is the first step but management is another issue altogether.  A HMSA survey in 2012 stated clearly members felt far better supported by an ‘expert in hypermobility’. This was regardless of whether it was a doctor, physio, OT etc. It was the knowledge that the professional they were seeing understood the hypermobility related components but also the certain truth that the professional they were seeing didn’t doubt their symptoms and experiences. There was an overwhelming sense of validation and relief from seeing someone they knew believed them.

           (All I want is to be believed. There is no point in going to my GP;

                  they just fob me off with pain killers and do nothing for me.

            I have no one to help me. I have been told I have been placed

            in the working group for ESA. I can’t work! I sleep all the time

                                      and I can barely walk.)


Distressed person is supported by another


Whilst we would like to see more specialist centres and more recognised ‘experts’ in all areas affected by a hypermobility syndrome, we acknowledge that in practical terms this would be difficult to achieve in the short term. What is not so difficult; is to ensure that all GP practices (and as many ‘other’ professionals too) are aware of hypermobility related disorders and HDCTs.  The HMSA hopes that with better training opportunities and by raising awareness of the hypermobility related disorders that rapid diagnoses can be made, which will reduce a lifetime of negative experiences of the patient in their health, medical and social care professionals.

                (My child is ill. She is always tired, complaining of stomach

                  ache, feeling sick and says her legs hurt. Yet the GP says

                    there is nothing wrong and I am making my child ill!)

Person at a lecterm addresses an audience


Some people undoubtedly will need to be seen by specialists, who may or may not be experienced or believe in hypermobility related disorders. These people will always benefit by being confident that their GP can successfully navigate alongside them, ensuring that they see the right people, at the right time. The GP with knowledge of the hypermobility spectrum disorders will be able participate in the management discussions that will need to be had.

                      (Hello, hello? I need help now. I need to speak to

                 someone urgently. My GP said there is going to be a meeting

            about my child with school, him and her physio with social services.

                                        I haven’t done anything!)

Sadly, at the moment our community is often labelled as being neurotic and making up symptoms in ourselves and our children. Yet in the experience of the HMSA, it is the GP’s lack of knowledge on the subject of hypermobility related disorders, and the potential complexities that is the real issue.

          Child being examined by a doctor

Many parents have wrongly been referred to social services and taken through the safeguarding processes, an ordeal which causes unnecessary stress to the child, parents and extended family. The safeguarding processes involve looking into everyone in the family, whether affected by a hypermobility issue or not.

               (I moved out of Wales to get away from everything because

             we weren’t believed. Now I have moved here and they still don’t

            believe me and what’s more they know about the Social Services

                 case. She is ill! I am not making her ill. Who can help me?)

This distress continues once the safeguarding process is completed; even when it is found that there is no case to answer.  Some people move away, to try and start again but find that the information is readily available wherever they go.

Parents rightly feel angry and it is not uncommon for those involved, to feel traumatised by such events. It colours their current and future relationships with health and medical professionals. Causing a lack of trust and confidence where it is so desperately needed.

       

        (It doesn’t matter that this is supposed to be finished now. There is

  still a file for my child, where I was accused of hurting him. Everyone knows

    at the school and in the village. I am so embarrassed. I feel like I am being

 judged and for what? My child was actually in hospital for 6 weeks! They said

                              he needed to be admitted, not me!)

To complicate things further depression and anxiety is high for people with these conditions. New research suggests that there is underlying biological reasons for this in hypermobility spectrum disorders. It is known that other chronic pain populations also experience high levels of depression and anxiety. But there is little recognition for those with a hypermobility related disorder where depression and anxiety can be overwhelming issues to cope with, whilst also facing other severe and debilitating symptoms.

           anxiety wordcloud of psychological symptoms

          (I have suffered from depression and anxiety for as long as I can

        remember. It can be hard to get up in the morning in pain and feeling

        like I haven’t slept. I can see no future. I don’t think anything will

                                   change. What is the point?)

The HMSA is always here to provide support to anyone with one of the hypermobility spectrum disorders or heritable disorders of connective tissue. It doesn’t matter which one because “There is room for everyone under our umbrella!”

       (We want to make a difference for

        people who are already diagnosed

        and for those who are yet to be so!) 

We believe that it is possible to ‘Give GPs the Tools’ and the resources they need to assist their patients on a daily basis. But to do this we need you to help us.

Doctor welcomes someone to his office

There are multiple aims for this campaign and we hope that you will feel able to support our work in assisting to raise the funds, so that we can meet the targets below.

  • We will assist  people with the conditions  we support, by providing educational resources to GPs. We will provide an introductory pack of information on all the conditions currently under the HMSA umbrella and the management of these conditions. This will reduce negative and inaccurate medical decisions, prevent and reduce inappropriate safeguarding referrals, ensure GPs have the latest evidence based information to inform their decision-making.

  • We will encourage GPs to make a diagnosis themselves, cutting down the delay for patients and allowing speedy access to services patients may need. This will also reduce the economic cost to the GP practice and allow for the patient to be confident in the ability of the GP.
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  • We will assist in determining who needs to be referred to specialist services, whether local or national. We will do so by providing a clear pathway, enabling GPs to assist patients in being sent to the right professionals and  at the right time.


  • We will provide and build on the HMSA’s website with view to it being a resource for GPs to, in which they can signpost their patients too,  whilst  remaining confident in the fact that the HMSA holds the NHS England accreditation, Information Standard.     


  • We will build on a professional specific resources on the HMSA website, which will assist GPs by providing documents and importantly, video presentations of lectures at professional conferences associated with the HMSA. This will allow GPs to see the latest information on a variety of multi-systemic issues that affect their patients.


  • We will provide opportunities for HMSA Professional Masterclasses, training and mentoring under the HMSA Kent Model and peer support via the HMSA Professional Hypermobility Network.

  • Providing back up to GPs for their patients by providing a host of support mechanisms, which they can be confident in using to support the needs of  patients, such as; local support groups, self-management programmes, helpline and access to social media specific support, It will make a difference to those of you already diagnosed and those who remain undiagnosed today!

  Team high five, working in partnership

This will make a difference to all of you who are already diagnosed and to those people who have yet to be! 

Please give to the HMSA! Every penny does matter. 

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Megan Lewis

Total raised:
£0.00 (excl Gift Aid)

  

Total donations: £1,617.52

Anonymous

10.12.18

£40.00 (+ £10.00 giftaid)

Anonymous

25.10.18

£231.00

The donation is from staff at Derry City and Strabane District Council

Sarah

21.05.18

Anonymous

16.05.18

£10.00 (+ £2.50 giftaid)

Anonymous

29.03.18

£181.52

From Everyone at The PCMS Group Ltd

Anonymous

22.03.18

£50.00 (+ £12.50 giftaid)

Anonymous

28.02.18

£10.00

Charlotte

16.02.18

£5.00

Andreas Paschos

31.01.18

Anonymous

11.01.18

 

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