I had to check and double check the day and date. Not being here yesterday threw me off a bit.
Can I just say OMG- I was so amazed at the Documentary? It was amazing seeing it all finished. Truly. I was good, I didn't cry although I did get choked up at one point when there was a photo of Scott when he was about 4 or so. Seeing him then, and then on the screen when he was so sick at 15, and how his is now. It was pretty intense. The doc. covered so much info, both from a medical perspective and the human perspective. The dr interviews always make me mad and frustrated, because it seems so futile. These drs try so hard and the IDSA/conventional medical community is resistant to the facts. The human/patient part was a mix of sadness and strength. it was shocking to see how sick Scott was, how he looked, how he talked.
I was in it much more than I expected. I thought I was going to be a "passing glance" but I had several appearances. My favorite ironic quote was when I had said (paraphrasing) that I would never wish cancer on anyone, but with cancer, there is support; medical, financial, health insurance coverage, ribbons galore. With Lyme- nothing.
This was before I was Dx'd with cancer and let me tell you, I stand by that statement 100%, esp this month being "Pink-tober." Lyme patients would love to have a month dedicated to Lyme awareness and fundraising. Technically May is Lyme Awareness month, but you would never know it. It is aways an odd feeling when I put on my Lyme awareness Alex and Ani style bracelet with my Relay for Life bracelet. It is indicative of the situation. The Lyme bracelet was made by a Lymie, trying to raise funds on her own (I did the same with my Lyme in the Coconut body care line) The Relay one, mass produced instantly recognized symbol and all that.
Well, this doc. is one additional step in the larger picture and I am so proud to be part of it. The doc is going to be available to the public after it screened and hopefully it will help.
So that it the Lymie part of my life. Today is the breast cancer part of it. Off the breast surgeon for another 6-month follow up. I will be most likely getting my script for a breast MRI. I am going to see if this can be my last follow up as long as the MRI comes back clear. I am kinda of done with drs. heh.
I better get in the shower, but i will come back and catch up with everyone soon!
Can I just say OMG- I was so amazed at the Documentary? It was amazing seeing it all finished. Truly. I was good, I didn't cry although I did get choked up at one point when there was a photo of Scott when he was about 4 or so. Seeing him then, and then on the screen when he was so sick at 15, and how his is now. It was pretty intense. The doc. covered so much info, both from a medical perspective and the human perspective. The dr interviews always make me mad and frustrated, because it seems so futile. These drs try so hard and the IDSA/conventional medical community is resistant to the facts. The human/patient part was a mix of sadness and strength. it was shocking to see how sick Scott was, how he looked, how he talked.
I was in it much more than I expected. I thought I was going to be a "passing glance" but I had several appearances. My favorite ironic quote was when I had said (paraphrasing) that I would never wish cancer on anyone, but with cancer, there is support; medical, financial, health insurance coverage, ribbons galore. With Lyme- nothing.
This was before I was Dx'd with cancer and let me tell you, I stand by that statement 100%, esp this month being "Pink-tober." Lyme patients would love to have a month dedicated to Lyme awareness and fundraising. Technically May is Lyme Awareness month, but you would never know it. It is aways an odd feeling when I put on my Lyme awareness Alex and Ani style bracelet with my Relay for Life bracelet. It is indicative of the situation. The Lyme bracelet was made by a Lymie, trying to raise funds on her own (I did the same with my Lyme in the Coconut body care line) The Relay one, mass produced instantly recognized symbol and all that.
Well, this doc. is one additional step in the larger picture and I am so proud to be part of it. The doc is going to be available to the public after it screened and hopefully it will help.
So that it the Lymie part of my life. Today is the breast cancer part of it. Off the breast surgeon for another 6-month follow up. I will be most likely getting my script for a breast MRI. I am going to see if this can be my last follow up as long as the MRI comes back clear. I am kinda of done with drs. heh.
I better get in the shower, but i will come back and catch up with everyone soon!