Most of us will probably know a few people in our lives who we could describe as being double-jointed – they can do ‘party tricks’ like contorting their bodies, are incredibly flexible, and can move their joints beyond a ‘normal’ range of motion. If that’s the case, the reality is that these people may have a mild form of hypermobility.
General joint hypermobility is not uncommon, often affecting the elbows, wrists, fingers and knees, and carrying no pain or medical complications. For 3% of the population, however, their hypermobility can be more extreme, and a sign of a more serious genetic condition called Joint Hypermobility Syndrome (JHS). JHS is a connective tissue disorder, which is often accompanied by joint pain, joint and ligament injuries, fatigue, and poor balance, alongside many other troubling symptoms.
Collagen is the protein that adds flexibility and strength to your skin, joints, ligaments and tendons, and is otherwise known as the ‘glue’ that holds your entire body together. In people with JHS, their ligaments, which are the thick bands of tissue responsible for holding the joints together and preventing them from moving too much or too far out, are much stretchier and weaker, because there is a defect in the way that their collagen is formed, leaving them with faulty or weak collagen. If you have joints that are far more flexible than normal and it causes you pain, you may be suffering from JHS.
Being diagnosed with JHS can be daunting and confusing, and many people are unsure what the implications are for their overall health and wellbeing, their quality of life, and their ability to participate in work or exercise. Our podiatrists are experienced in working with many patients with JHS to support them in managing their joint hypermobility and any knee, hip or ankle problems that may arise, so they can continue to live and work as normally and safely as possible, and with as little pain as possible. As hypermobility can change over time, working with a trusted podiatrist who understands your unique situation and condition is important to ensure that you are future-proofing your body’s health and protecting your joints against any future injury.
The most common symptom of JHS is extreme flexibility and pain in your joints and muscles, but other symptoms can include:
JHS is caused by your genetics – it tends to run in families and is an inherited condition. It is believed that if one parent has hypermobility, one in two of their children will also have it, and the genes that are responsible for creating collagen throughout the body are believed to play a role. Hypermobility can also be influenced by:
To be diagnosed with JHS, you will need to visit a podiatrist or other health provider to undergo a physical exam, to assess the range of motion in your joints and discuss your health history and other medical issues. They may also request blood tests to rule out any other possible genetic conditions.
Typically, a questionnaire called the Beighton Hypermobility Score will be used to measure the flexibility of your joints, by asking you to perform certain tasks. You will be asked to try to do exercises such as bend forward and place your hands flat on the floor without bending your knees, bend your thumbs backward to touch your forearms, and bend your little/pinky fingers backwards as far as you can.
As everybody (including people with JHS) experiences lessening flexibility as they get older, you may also be asked how hypermobile your joints were when you were younger. Questions may include, “Can you now (or could you ever) bend your thumb to touch your forearm?”, “As a child, did you amuse your friends by contorting your body into strange shapes or could you do the splits?” and “As a child or teenager, did your shoulder or kneecap dislocate on more than one occasion?”. If you answer yes and are able to do a range of activities displaying extreme flexibility, you may be diagnosed with JHS.
Unfortunately, Joint Hypermobility Syndrome cannot be prevented, or cured, because it is a genetic disorder that you inherit at birth. However, it’s encouraging to keep in mind that as people get older, their flexibility naturally decreases and their symptoms tend to improve. For some people, symptoms are mild, but for others, the pain can be severe, and everyone’s hypermobility affects their bodies in unique ways, so it’s important to work with a trusted podiatrist team to learn ways to protect your joints and manage your pain.
If you have JHS, it’s important to maintain a healthy lifestyle and protect your joints. You can improve your joint and muscle strength by:
There is a wide variation in the shape of the foot in people who are hypermobile. Most tend to have flat feet but a few have a high-arched foot, which can cause pain and problems when walking. In addition to this, patients with JHS experience higher rates of osteoporosis in their joints. Hypermobility in your feet, knees and hips can also increase the likelihood of strains, sprains and dislocations in these areas.
While there’s no cure, all of these preceding issues can be managed, and many people with JHS can live a full and active life when working alongside the support of an experienced podiatrist who understands your condition, and is able to prevent and treat further pain and injuries with a wide range of proven techniques, assessments and strategies, to reduce your symptoms and and improve your quality of life:
Are there different degrees or types of hypermobility?
Yes, hypermobility can vary in degrees and types. The Beighton scale is commonly used to assess hypermobility, which involves evaluating joint flexibility and assigning a score based on specific movements. There are also different types of hypermobility syndromes, such as Ehlers-Danlos syndrome (EDS), which is a group of inherited connective tissue disorders characterised by joint hypermobility, skin hyperextensibility, and other associated symptoms.
What are the potential complications or associated conditions with hypermobility?
Hypermobility can be associated with various complications and conditions, including:
Are there any long-term effects of hypermobility if it is unmanaged?
For some yes, and for others no. If left untreated, for some hypermobility can lead to long-term effects including chronic pain, joint instability, and an increased risk of joint damage and arthritis. Untreated hypermobility can also impact daily activities, quality of life, and overall function.
What lifestyle modifications can help with hypermobility?
Adopting certain lifestyle modifications can help manage hypermobility symptoms. These may include:
What footwear recommendations are suitable for individuals with hypermobility?
When it comes to footwear recommendations for individuals with hypermobility, it’s generally beneficial to prioritise stability and support. Consider the following:
Is there a risk of developing arthritis or joint degeneration with hypermobility?
Yes, individuals with hypermobility, particularly those with certain connective tissue disorders like Ehlers-Danlos syndrome, may be at a higher risk of developing arthritis or joint degeneration. The excessive joint movement and instability associated with hypermobility can contribute to increased wear and tear on the joints over time. It’s essential to manage hypermobility and seek appropriate medical care to minimise the risk of joint damage and related complications.