Vaccination for COVID-19

Over the last year and a half many anxious parents around the world, have been asking why those who have Floating Harbor Syndrome (FHS) have not been classified for inclusion in a high priority group, within the vaccination programs relating to COVID-19.

The advice we have to date, is that all persons with a formal diagnosis should be vaccinated as a high priority case. At the time of writing this information applies to ages 12 upwards.

Pending further investigation in this category of neurodiversity and genetic complexity, individuals with FHS must be considered as having a higher risk of contracting serious side effects due to the virus and should be treated as such. Most individuals with FHS have Developmental Delays and the CDC supports the advice given: –

“Some people with developmental disabilities may have difficulties accessing information, understanding or practicing preventative measures, and communicating symptoms of illness”.

We strongly advise that all Health teams around the World acknowledge that FHS individuals are in urgent need of protection in this area because failure to provide vaccinations to them may have a detrimental effect on their quality of life.

What FHS individuals must endure to live life are unique within their classification and are not duplicated within any other groups, or anywhere else for that matter.

Action must be taken now.

Staying Safe

With the Covid pandemic continuing world-wide, we all have to do what we believe is best for our family in keeping them safe.

Different countries have different instructions on staying safe when around people, so it is not a one fits all rule anywhere.

When it comes to Floating Harbor Syndrome, there is no current data available on whether your child is more susceptible to getting Covid or not, however given that this is a Developmental Delay, that has many complications, should alert the medical professionals to err on the side of caution and offer vaccinations to our children quickly.

One parent reports that they enquired about getting a vaccination for their FHS family member, to be told that the ‘condition’ has to be on the Government’s Medical List to be registered to receive their shot early.

The way to approach this, as FHS is so rare, is to contact your own family doctor, and ask them to intervene, requesting support for your child to get vaccination. It is because of the ‘unknown’ that should prompt urgent action.

Medical List from the CDC

Population Risk Assessment UK

COVID 19 and FHS

There is no evidence available to suggest that anyone with Floating Harbor Syndrome should or should not have to wear a mask during this pandemic.
It comes down to the choice of the parent/guardian, on what is the best solution for their child.

Please stay safe and get in touch if you have any other concerns.

Thank you

Jeans for Genes Day 21 September 2018


Jeans for Genes Day is the annual fundraising campaign for Genetic Disorders UK, the national charity that supports individuals and families affected by a genetic disorder.

Monies raised on Jeans for Genes Day fund the work of the charity and provide grants to organisations for projects that aim to transform the lives of children with genetic disorders.

Supporting our network through


FHS child thinks being bullied is normal

One of our members reports that their child was bullied throughout Nursery and Primary School. The child had a formal diagnosis of Floating Harbor Syndrome at the age of 4, yet teachers would punish the child for not listening in class or not responding appropriately to instructions. The child in question also has an intellectual disability, a diagnosis of ADHD, amongst other complex needs –  specialised support was denied to the child throughout their schooling. Floating Harbor Syndrome was laughed at by professionals, all because of its name! Children threatened the child, verbally and emotionally bullied the child, and sadly, they were hit physically by other children in the playground and on the journey home. The child could not express their feelings to anyone for years, as they have social communication issues alongside their Learning Disability. The schools could not do anything, as the child was unable to recognise the people responsible, therefore washed their hands of the problems that continued for 8 years.

This all happened in mainstream education in Scotland.

Education Suggestions

Remember the 5 ‘R’s – Learning by visual representation, routine, repetition and reinforcement/reward with praise.

Representation: Children with Floating Harbor Syndrome respond and learn using touchable props. When teaching maths, use objects to help build mental representations for the child. Visual learning is key to their cognition. Making sense of numbers and how they interact depends very much on this strategy. Using fingers should be encouraged also; anything that makes it interesting and fun. For reading and learning phonics, the use of pictures is important. This need for representation of objects and pictures is required throughout their schooling life; nursery right through to secondary/college.

Repetition: The set educational curriculum has to be adapted specifically for the FHS child. This has been reported in many cases and should be adhered to where possible. Typically FHS children really struggle to learn at the expected levels of progression set by Local Authorities in the UK. It takes years for the child to grasp the basic concepts of numbers, letters and the meaning of school. If the child struggles in Primary 1, they will be overwhelmed in the next year of Primary 2, therefore be prepared for covering the same material each year until there is a fuller understanding. It is not about going backwards in learning, far from it. Repeat the work and move up a notch each time, perhaps moving a reading book up to the next stage or asking more questions in a workbook. The FHS child will respond to recurring themes and gain in confidence and self-esteem and if they are accomplishing more each time then this is great; if not, go back to the work where they started and build up again. Repetition is closely linked to Routine, which is looked at next.

Routine: There are similarities with children on the autistic spectrum, in that the FHS child needs to have a routine and that if there is to be change, they are told about it in advance (and repeat). They expect life to be the same and can appear anxious and lack in confidence when challenged with something unexpected. If they are used to tackling a task in a certain way, then this is what they are confident with and crucially feel secure about, therefore if change has to happen, approach this in small steps, constantly reassuring the child that they can succeed. Strategies, including photographs and pictures to provide a visual plan of the day’s activities to avoid anxiety.

Reinforcement/Reward: Praising a child for good work done is well received by all, but children with FHS need constant praise, encouragement and reward. In this regard, reward comes from achieving set goals; for a teacher this could mean moving to a new reading book or by giving the child a ‘well done’ sticker. If the child is not progressing at the pace which the teacher sets, then go back to the beginning as stated in Repetition. Withholding or denying the child access to routine events, like break time or fun activities, will have a detrimental effect on the child, which should be avoided at all costs. Their understanding of why they are being punished is not the same as with average children. Learning levels will increase and decrease and there is no intention to deviate from the expected levels, rather they are struggling or are overwhelmed by the work.

It is extremely important to have your child assessed by suitably qualified professionals who are familiar with Floating Harbor Syndrome and the often ‘invisible’ issues that the child faces in their experience in an Educational environment. Specialist Schooling is advisable, as Mainstream Schooling often lacks the expertise required to properly manage the care of the FHS child, both emotionally and academically.

Thank you all

Over the last 18 months, there has been a massive increase in the number of parents and professionals getting in touch with us here on the website to ask about Floating Harbor Syndrome.

As more children are diagnosed, more information is shared on their development and in turn we strive to pass this on to as many people as we can. Some parents wish to remain anonymous and therefore do not wish photos of their children to be published anywhere on the internet, and we respect this fully.

Thanks for supporting our children