**Local Woman Diagnosed with Rare Tick-Borne Allergy After Severe Reaction**
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Angela Lundy, a resident of Ross Township, Pennsylvania, has been diagnosed with alpha-gal syndrome, a rare tick-borne allergy that can trigger life-threatening reactions to red meat, dairy, and gelatin. Lundy’s ordeal began shortly after a tick bite she received in early June while gardening in her backyard.

The initial signs of her condition became evident on Father’s Day when Lundy experienced intense stomach pain after consuming a bratwurst. Despite the discomfort, it was a week later, after she shared a burger with her husband, that the severity of her symptoms escalated. “I woke up with severe stomach pain right along where my bra line is, and it lasted about three hours,” she recounted. In her search for answers, Lundy sought medical advice, but her tests for gallstones — a suspected cause of her pain — returned negative.

It was during a conversation with a friend that the possibility of alpha-gal syndrome was suggested, albeit in a half-joking manner. The mention prompted Lundy to connect her symptoms with her recent tick bite. “It was the itchiest bite I had ever had,” she recalled, describing the moment she was bitten while tending to her garden.
The subsequent blood tests confirmed her friend’s speculation. Alpha-gal syndrome is known to be triggered by the bites of certain ticks, particularly the Lone Star tick in the United States. The condition has gained notoriety for its severe allergic reactions to meat and other mammalian products, transforming unsuspecting victims’ diets dramatically.
According to the Mayo Clinic, the allergy can vary in intensity, resulting in mild to severe reactions not only to red meats such as beef, pork, and lamb but also to dairy and gelatin-based products. Lundy expressed her determination to adapt to this new reality, stating, “It’s not fun, but I think there are worse things.” To safeguard against anaphylaxis, she now carries an EpiPen with her at all times.
Preventative measures against ticks are vital, as experts recommend wearing protective clothing that covers arms and legs, tucking trousers into socks, and opting for light-coloured garments to easily detect any ticks. Lundy has followed guidelines which advise that individuals avoid brushing against shrubbery and bushes where ticks frequently reside, and to apply insect repellent containing DEET, permethrin, or picaridin when venturing outdoors.
The Centers for Disease Control and Prevention (CDC) estimates that around 450,000 Americans may be living with alpha-gal syndrome. However, the true prevalence of the condition remains murky. Unlike many communicable diseases, alpha-gal is not subject to national notification requirements, meaning healthcare providers are not obliged to report cases to federal authorities. This lack of reporting could mean that many cases go unnoticed or undocumented.
Angela Lundy’s experience serves as a timely reminder of the potential dangers lurking in everyday activities such as gardening. While she has identified her allergy relatively early, many individuals may be unaware of the risks associated with tick bites. The increasing number of reported cases of alpha-gal syndrome, particularly in regions predisposed to tick infestations, suggests a growing need for public awareness and education on tick-borne illnesses.
In conclusion, Lundy’s story sheds light on the realities of living with a tick-borne allergy and highlights the importance of understanding and recognising the symptoms associated with such conditions. As more individuals find themselves affected by diseases stemming from tick bites, efforts towards awareness and prevention will continue to play a crucial role in public health.
