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SCS & Pain Pumps For spinal cord stimulator (SCS) and pain pump discussions. |
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Hey everyone
Sorry for yet another question--they just keep popping into my head. I'm wondering if any of you have ID tags stating that you have a SCS. Obviously I am months or years away from that point... still in the first stages. I had to get a medical ID bracelet (from Lauren's Hope) after my gastric bypass surgery. I also have on there that I have a ceclor allergy. I am thinking about getting a new tag if I ever get some money, because I have a sensitivity (not allergy) to latex and would like to put that plus an emergency contact on my bracelet. I am just wondering if your doctors suggested putting this information on an ID tag. If so, I will wait a little longer to get a new tag in case I end up with an SCS--they are expensive and since I have no income, I don't want to have to keep buying new ones to add more info. Thanks! Sarah
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. ♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥ My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems. |
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