He’s absolutely right, but there’s way more. If you think you have it, get tested by a Lyme literate doctor or practitioner!! It’s living hell, and I’ve had breast implant illness, autoimmune diseases, surgeries from organ failure, mold toxicity, and now Lyme (umbrella term) plus a live form of Babesia. I’m 68, and haven’t been well for over 20 years. It costs a LOT: money (out if pocket costs for almost everything), people who work for you sometimes take advantage of you because they see a target, and I’m only 4’ 9”, disbelief from people who’ve never been sick like this, horrible pain, cognitive impairment, loss of your family (mine, anyway), accusations of taking drugs (I was put in rehab when I was actually getting Sjogren’s), friends, relationships, and for me, the loss of my beloved teaching career, so loss of identity, a good income and colleagues, etc. I’ve become isolated for the most part because I can’t plan on how I’ll feel every day, and exercise makes me worse, except for stretching. My house is a mess right now, because two people just moved out that had mold in their home. In addition, I broke my humerus 10 1/2 months ago, and because of the restricted blood flow, it’s still not healed, and I’m not supposed to use it. I live alone and want to take good care of my house, but I can’t. I have to pay someone to do things that I don’t mind doing, so I’m behind in exterior maintenance, overwhelmed with everything, money issues, taxes, etc., and there is no understanding nor help for us from hospitals, regular doctors, and people, don’t believe someone could be sick this long with overlapping conditions one after another. I can’t even deduct household help from my taxes for my broken arm. Sometimes I lay and stare at the wall because I’m so scared, anxious, and depressed. This is no joke. I’m trying to make people aware of this through my comments, so I apologize for my long comment if you’re still here❣️🙏🌷
@danielleperry1657 I’m going to look him up!!! My doctor is all about numbers; no psychological help, sometimes she suggests supplements, but I’m concerned that when I told her there was physical abuse from my grown son who stopped his Lyme medications from a different doctor where he was getting ozone treatments, etc., she said, “I don’t have a pill for that.” The next time she did say she was sorry about the issue when I said it again. He’s now in jail because he decided he didn’t want nor need treatment anymore. Sick of being sick and too proud to admit he was sick (especially psychologically!!). I know if you stop treatment, it comes back, which I think happened to him: went into rages, mania, psychosis, and is so very distorted. We found out he had Lyme meningitis at age 7, and is now 37. Yet the CDC and doctors keep this under wraps. WHY?!
He’s absolutely right, but there’s way more. If you think you have it, get tested by a Lyme literate doctor or practitioner!! It’s living hell, and I’ve had breast implant illness, autoimmune diseases, surgeries from organ failure, mold toxicity, and now Lyme (umbrella term) plus a live form of Babesia. I’m 68, and haven’t been well for over 20 years.
It costs a LOT: money (out if pocket costs for almost everything), people who work for you sometimes take advantage of you because they see a target, and I’m only 4’ 9”, disbelief from people who’ve never been sick like this, horrible pain, cognitive impairment, loss of your family (mine, anyway), accusations of taking drugs (I was put in rehab when I was actually getting Sjogren’s), friends, relationships, and for me, the loss of my beloved teaching career, so loss of identity, a good income and colleagues, etc.
I’ve become isolated for the most part because I can’t plan on how I’ll feel every day, and exercise makes me worse, except for stretching.
My house is a mess right now, because two people just moved out that had mold in their home.
In addition, I broke my humerus 10 1/2 months ago, and because of the restricted blood flow, it’s still not healed, and I’m not supposed to use it.
I live alone and want to take good care of my house, but I can’t. I have to pay someone to do things that I don’t mind doing, so I’m behind in exterior maintenance, overwhelmed with everything, money issues, taxes, etc., and there is no understanding nor help for us from hospitals, regular doctors, and people, don’t believe someone could be sick this long with overlapping conditions one after another. I can’t even deduct household help from my taxes for my broken arm. Sometimes I lay and stare at the wall because I’m so scared, anxious, and depressed.
This is no joke. I’m trying to make people aware of this through my comments, so I apologize for my long comment if you’re still here❣️🙏🌷
@danielleperry1657 I’m going to look him up!!! My doctor is all about numbers; no psychological help, sometimes she suggests supplements, but I’m concerned that when I told her there was physical abuse from my grown son who stopped his Lyme medications from a different doctor where he was getting ozone treatments, etc., she said, “I don’t have a pill for that.” The next time she did say she was sorry about the issue when I said it again. He’s now in jail because he decided he didn’t want nor need treatment anymore. Sick of being sick and too proud to admit he was sick (especially psychologically!!).
I know if you stop treatment, it comes back, which I think happened to him: went into rages, mania, psychosis, and is so very distorted. We found out he had Lyme meningitis at age 7, and is now 37. Yet the CDC and doctors keep this under wraps. WHY?!
And I went to the doctor and they don’t listen around here
I’m so sorry to hear how much you are suffering. Just take one day at a time. Maybe you can recall happier days and dwell on these memories.
All this time . I got questions for sure
Do some research! Find a Lyme literate practitioner and get tested.