Fampridine recommended for use on the NHS in Scotland

Please note: The current Coronavirus Covid-19 pandemic is fast moving, and reactions to it seem to update not just day-by-day but minute-by-minute. Obviously, this site was not designed to bring you the very latest developments in a ‘breaking news’ story such as this. Instead, this site will continue to include news and opinions relating to major events, policy changes, and so on.

——————————————————————————————————–

Fampridine (brand name Fampyra) has been given the green light for use by the NHS (National Health Service) in Scotland to treat people with MS who have a walking disability. Approval was given by the SMC (Scottish Medicine Consortium) despite a warning issued by the US’s FDA (Food and Drug Administration) regarding an increased risk of seizures.

The drug was approved by the FDA in January 2010 to improve walking in individuals with MS. Known side effects are seizures which have an increased risk of occurring with higher blood levels of the drug. The FDA is currently updating the drug label to advise that kidney function should be checked before starting; and monitored once a year during the course of the treatment. Kidney impairment may cause an elevated blood level of the drug, which can increase the risk of seizures.

In Scotland, one of four countries that make up the United Kingdom, fampridine will be available to people who are scored 4-7 on the Expanded Disability Status Scale (EDSS). The treatment is taken as a tablet.

Scotland is the second UK nation to offer this treatment on the NHS following a decision in Wales to make fampridine available on the NHS for adults with MS.

What is fampridine?

The MS Society says fampridine is an SMT (symptom management treatment) meaning that it helps people with the symptoms of their MS as opposed to DMTS  (disease modifying therapies) which control the condition itself. Most people are prescribed one tablet in the morning and one at night. It helps about one in three people who take it and can speed up walking by about 25%.

In double-blind phase III studies it improved walking ability in adults with MS and walking problems, compared to placebo.

Rest of UK must follow suit

MS Society director in Scotland, Morna Simpkins.

MS Society director in Scotland, Morna Simpkins, said: “It’s fantastic that fampridine (Fampyra) has been approved for use on the NHS in Scotland. This treatment could be life-changing for many people living with the symptoms of MS – making an important difference to walking and energy levels.

“We are delighted to hear that SMC has accepted the drug but it’s up to our health boards to make sure people who could benefit can get it.

“We hope appraisal bodies in other parts of the UK follow suit as soon as possible, so everyone with MS can access fampridine when they need it.”

MS Society Scotland also highlighted the following fampridine success story:

Fampyra helped Nina dance at daughter’s wedding

Nina is from the Shire ofInverness. She used to be an Occupational Therapist and has been living with MS for over 25 years. She began taking fampridine (Fampyra) when she moved to the Highlands and has seen a huge positive impact.

Nina told us: “It’s fantastic news that Fampyra will now be available for people with MS on NHS Scotland. I’ve seen first-hand the positive impact it can have so to know that it should now be an option for more people across the country is really welcome.

Nina. (Pic: MS Society).

“When I was first told I’d progressed from relapsing remitting to secondary progressive MS my consultant at the time simply said, ‘there’s nothing to do, just look after yourself’. But when I moved further north I had a new consultant who suggested I try Fampyra and it’s been brilliant.

“I am quite sensitive to drugs so I’ve had to gradually work my way to taking the full therapeutic dose, but it’s had such a huge impact it was worth the effort.

On my daughter’s wedding day I didn’t have to use my wheelchair at all and Fampyra definitely played a role in that. Even when the dancing started I was still standing!

“One of the main symptoms I experience is shortening of my right Achilles tendon which gives me difficulty walking, so I wear a splint and use two sticks when I’m outside and a wheelchair for longer distances

“Since starting Fampyra I have had more movement in the toes of my right foot, which I hadn’t been able to do for years. And the progression of my condition has been much slower, I have more energy and just feel able to do so much more.

“It still takes a bit more time and I need to think and plan ahead for most activities, but I’m now able to walk further for longer. It helps me feel stronger physically and mentally – it’s like having more charge in the battery.

“I’m a fiercely independent person so it’s been great. I took up a six month, part-time last year which has paid for a new wheelchair, something I wouldn’t have considered without the treatment. My family now feel more confident about my safety and that they don’t need to offer as much support which is brilliant.

“One of the most fantastic things was on my daughter’s wedding day I didn’t have to use my wheelchair at all which I had fully expected to and Fampyra definitely played a role in that. Even when the dancing started I was still standing!

“A treatment like this is invaluable and so positive, the more people who want to and can access it, the better.”

* * * * * * * * * * * * * * * * * * * * * * * * * * * * * ** * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * *

Spelling

Please note that being born in the UK, all my posts, are written using British English spelling.

For example:

Centre                              not center (except in names, Centers of Disease Control)                  Colour                              not color                                                                                                                      Diarrhoea                       not diarrhea                                                                                                  Haematology                not hematology                                                                                Haematopoietic          not hematopoietic

* * * * * * * * * * * * * * ** * * * * * * * * * * * * * ** * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * *

50shadesofsun.com is the personal website of Ian Franks. He enjoyed a successful career as a journalist, from reporter to editor in the print media. He gained a Journalist of the Year award in his native UK. More recently, he was a freelance medical writer and editor for various health information sites. Ian received a diagnosis of MS in 2002 and now lives in the south of Spain. He uses a wheelchair and advocates on mobility and accessibility issues.

* * * * *

Note: Health-related information available on 50shadesofsun website is for your general knowledge only. It is not a substitute for medical advice or treatment for specific medical conditions. Ian is not a doctor, so cannot and does not give you medical advice. You should seek prompt medical care for any specific health issues. Also, consult a doctor before starting a new diet or exercise programme. Any opinions expressed are purely his own unless otherwise stated.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s