I love the tiny feet of my daughters - they're soft, round and perfect. Those little feet have so far to go, so many kilometers to travel. As individuals, our girls have such amazing adventures to embark on and I will do my best to never hold them back, remembering always that their lives and loves are their own to discover. I will guide them as best as I can, I will love them with all of my heart and I will encourage them to be the people they want to be.
Showing posts with label auto sanguis therapy. Show all posts
Showing posts with label auto sanguis therapy. Show all posts

Monday, March 7, 2011

A new day, a new therapy!

Auto Sanguis therapy here we come!

E started with a sore throat on Thursday; which progressed to a barking croup cough on Saturday night and so the saga continues....

We met with Uwe today, and we start the drops that have been made up in response to her own blood, tomorrow morning. Am excited (as excited as one can be when one's child is ill) about this new therapy, and very interested in how it will pan out. Most importantly, I'm positive, very positive :-)

Wednesday, March 2, 2011

Coughs, doctors and remedies


It always amazes me how, once one has made a decision, life looks a little rosier. It may not be the 'right' decision (how would one know?) and it may not be the easiest decision. But it's a decision...

After 2 years and 4 months of E's on/off coughing (mostly on), thousands of rands spent on medical bills, countless sleepless nights, an increasing number of grey hairs and wrinkles, I've come to a point where I can no longer continue. I cannot continue to see her cough the way she does every 3 weeks. More importantly, I can no longer expect her to continue in this same way.

We've tried new doctors and new remedies, from Western to Chinese to homeopathic. We've tried acupressure (not acupuncture) and kinesiology.
We settled on a combination of Chinese and homeopathic meds and alternate between kinesiology every month, and acupressure when the cough is bad.

But still that cough continues. This last time was the worst time and I've now put my foot down! Someone needs to do something. The homeopath is fantastic but she needs to do more. The kinesiologist is awesome but we can only see her once a month. Bottom line is that E has to go through this every month (as do we), she misses out on school, on parties, on seeing friends. She has 4 days a month when she cannot eat, sleep or speak. I, as her mother, cannot see her go through this again - or not this often, anyway. I worry about the long term effects of such a cough. And so, in true mom fashion (because let's admit it - it's what moms do - not the specialists, but the moms) I started to look for something more.