Author: Adrienne Ritchie

MyViewPoints: Sharing information, connecting communities

Adrienne found online communities helpful when recovering from Lyme disease

About two years ago I became very sick. After dealing with illness for a number of months I was finally diagnosed with Lyme disease. Suddenly I had an explanation for all the symptoms I was feeling: aches and pains, headaches, blurred vision, dizziness, memory loss, upset stomachs, anxiety, depression.

I was lucky to find a great local doctor and have a supportive network of friends and family to lean on. I took my prescribed antibiotics and felt better. I took time off from work and gave my body time to heal. Both played into my eventual recovery, as did the support network I found online. By connecting with an online Lyme disease community I learned what hurdles other people like me were facing, and how they beat (or at least coped with) those hurdles. I asked questions like what homeopathic remedies worked best for them? How did they alleviate anxiety? How were they able to ease the upset stomachaches caused by their antibiotics?

I was helping myself get better, and after a while started sharing my own remedies and coping mechanisms. The back and forth developed into strong, supportive relationships that were very important to me. They didn’t take the place of a trip to the doctor’s office or real life bonds I had, but it was so helpful to have access to people who understood my ups and downs, didn’t mind my occasional venting and were so eager to share information.

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