Pertussis (whooping cough) is a highly contagious disease of childhood (R0 15–17, comparable to measles) transmitted by respiratory aerosols, with the principal vectors of transmission being asymptomatic adult carriers of the bacterium Bordetella pertussis.
Pertussis was first reported in France in the 15th century, and Bordetella pertussis appears to have emerged from or in parallel to the agent of kennel cough (Bordetella bronchiseptica) in dogs.
Although pertussis mortality is dramatically reduced in economically privileged societies from 19th century figures, with the disease today typically modest in its appearance, the disease can be debilitating & terrifying, warranting efforts at prevention worthwhile.
Pertussis mortality in economically privileged societies decreased precipitously in the early 20th century well before introduction of the whole-cell pertussis vaccine in 1948,
likely due to improved living conditions in general, in parallel with a reduction in all-cause childhood mortality.
Following introduction of the whole-cell pertussis vaccine (the pertussis component of the DPT) in 1948, the incidence of reported pertussis cases declined dramatically.
It’s likely that one partial explanation for the extremely low rate of reporting of pertussis in the 1970s-1980s, was underreporting due to provider unfamiliarity with pertussis & failure to diagnose other than severe cases, under the assumption that pertussis had been “eliminated” by near-universal vaccination. In the 1940s-1950s we all had it as children, but physicians in the 1970s-1980s largely assumed it was “gone” and were not well positioned from their training to recognize garden-variety cases.
The association of the DPT vaccine with infantile seizures in the 1980s (attributed by the industry, and widely accepted within conventional medical circles to have been the coincidence of the onset of idiopathic epilepsy with the vaccination schedule) resulted in the National Childhood Vaccine Injury Act of 1986, and the replacement of the whole-cell pertussis vaccine with an acellular preparation targeting the pertussis exotoxin in the Dtap and Tdap vaccines in current use. These, unlike the whole-cell vaccine, do not induce sterilizing immunity & do not impact significantly on community transmission, resulting in a modest “rebound” of pertussis in recent years.
The current CDC vaccination schedule calls for an initial dose of the Dtap vaccine at 2 months, boosted at 4, 6, and 15 months:
Protection from birth - 2 months, a population in which the disease is most concerning, is dependent on maternally-conferred passive immunity. In the era prior to vaccination, women of childbearing age universally possessed “lifelong” immunity from childhood infection, “boosted” by periodic asymptomatic exposure to pertussis circulating in the community, which could be passively transferred to the infant via transplacental & breastmilk transfer; this maternal exposure has been disrupted by widespread use of the DPT vaccine, and presently the Tdap vaccine is recommended to pregnant women at 27 through 36 weeks gestation to provide for the transfer of passive immunity to the infant for this critical period.
“Cocooning” is also often recommended, involving vaccination of older children & adults who may be in contact with the infant. This latter has proven ineffective, both due to impracticality of the logistics involved, and due to the ineffectiveness of the current pertussis vaccines (Dtap and Tdap) in providing sterilizing immunity. It might seem that preventing symptomatic pertussis might reduce the risk of community transmission, but the reverse appears to be the case; pertussis is transmitted by respiratory aerosols independent of cough or catarrh, and asymptomatic or minimally symptomatic adults (perhaps presenting with “common cold” symptoms), including those with presumed immunity from vaccination, serve as the primary (“stealth”) vectors of community transmission.
The Dtap & Tdap vaccines do not appear to be associated with the encephalitis & infantile seizures seen with the whole-cell pertussis component of the DPT. Although concerns exist with some regarding a presumed association of vaccination in general with autism, these appear to be unfounded, and originated specifically with the MMR vaccine, never implicating the Dtap vaccine.
Homeopathic management of Pertussis includes the treatment of cases according to the Totality of characterizing signs & symptoms, with one of a large (over 160) collection of potential remedies requiring some experience both with pertussis and with homeopathic case management in general, and short-term homeoprophylaxis, typically using a genus epidemicus when one can be discerned in a local outbreak (see aphorisms 101-104 in the Organon), or a “genus” remedy of Pertussis, most commonly Drosera rotundifolia. Although sometimes oversimplified as a task suitable for the home prescriber according to simplified “homeotherapeutic” protocols, this is a task for an experienced prescriber and is not to be undertaken lightly.
Recently I had 2 brothers where mom (student at Homeopathic school) is convinced that her both boys had pertussis. The whole family has 4 brothers, and they are unvaxxed family. Most of the case was taken via email and texts s with couple phone conversations mostly with mom. All the remedies were done as plussing (water doses). I would ask mom to do up to 5 doses and then report to me the response. The 17-year-old who had cough symptoms, I started with Rumex 200c on September 7, 2024, with improvement but symptoms returned so I switched to Rumex 1M on 9/11/24 with minor improvement. On 9/13, I recommended Spongia 200c, some improvement and then worse, so switched to Ant tart 1M on 9/22, then to Ars album 30c on 9/29. Best response so on 10/3 switched to Ars album 200c, improved but cough lingering. Towards the end is when mom said she thinks it is pertussis. The family refused to go to a licensed physician instead went to the acupuncturist and continued to see her 2x/week. As I was doing follow ups remotely thinking this was cough, I was puzzled as to why it was taking so long. When she said it seemed like pertussis, on 10/6 I asked her to start Pertussin 1M. He responded beautifully at that time. His brother, 14-year-old, I gave Drosera 30c on 9/30/24. Response was good. She did go to Pertussin 1M on 10/6 and that resolved both of their symptoms.
Thank you Will. Pertussis became very ‘real’ for me early this year when our 10 month granddaughter was affected. A very frightening time. They presented to hospital, where they were on holiday in rural Tasmania, and were told she couldn’t have whooping cough (she appeared quite well between coughing paroxysms) and refused to even test, an attitude that reflects what you say about the doctors not recognising it. Of course her case was then not reported which artificially lowers statistics of case incidence. Her brother and mum also were affected, her dad didn’t get it. It took the whole 3 months to fully recover for the baby girl, despite best efforts of their experienced homeopath.
Are the therapeutics of whooping cough something you have written about previously? Or records of cases you have treated?