Last week, we said that Neuros could supplement their income from pharma-related activities.
Next there was a flurry of emails, asking for disclosure of how much, if anything, I get from MS pharma and elsewhere.
Having skirted round the issue, as I am not discussing my personal life, the question is what happens to your income?
Whilst on an individual level, I think it is none of my business, but as I am sure you know, MS does not just cost you your health...but also your wealth.
Even more reason to make sure you deal with MS as best you can as early as you can.
Landfeldt E, Castelo-Branco A, Svedbom A, Löfroth E, Kavaliunas A, Hillert J. Personal Income Before and After Diagnosis of Multiple Sclerosis. Value Health. 2018;21:590-595
Multiple sclerosis (MS) is associated with serious morbidity and labour force absenteeism, but little is known of the long-term impact of the disease on personal income.
To assess long-term consequences of MS on personal salary and disposable income.
Patients with MS in Sweden were identified in a nationwide, disease-specific register and matched with general population controls. We assessed mean annual personal gross salary and disposable income each year before and after index (i.e., the MS diagnosis date) using data from national registers.
The final sample consisted of 5,472 patients and 54,195 controls (mean age 39 years; 70% females). There was no significant difference in gross salary between patients and controls in any year within the pre-index period. In contrast, on average during follow-up post diagnosis, patients with MS had €5,130 less gross salary per year compared with controls, ranging from a loss of €2,430 the first year to €9,010 after 11 years. Within 10 years after index, 45% of patients had at least one record of zero gross salary, compared with 32% for controls. Mean annual disposable income was comparable between patients and controls across follow-up, with significant differences only at years 9 and 10 post-index.
We show that many patients with MS in Sweden lose their ability to support for themselves financially but still have a relatively high disposable income because of social transfers. Our findings underscore the detrimental impact of MS on affected patients and the considerable economic burden of disease to society.
Whilst the figures are based on Scandi-health and may not be relevant to your particular country. It says that once diagnosed, eventually you are going to earn less and you are more likely to become unemployed. If you have a working social care system then there is some compensation for this
Labels: Cost of MS