Posted 11/29/2017 11:20 AM (GMT -5)
Girlie,
No there is no treatment for hand food mouth. Its a childhood viral disease that children just suffer through, and there are multiple strains so you can get it a few times. I'm thankfully getting over it, and it really just affected my mouth. I can't imagine how horrible it must be when its on your hands and feet too, and littles can get it on their bums!
Already planned on stopping the JK. I just really wish I could take it. It is hard to believe that even 1/8th of a drop can have this big of an effect on me, but I should believe it because this is the 4 time. I have it in my head that I have to take it or I am not going to get better. That, and I spent money on it that I don't want to waste.
If it causes such a reaction doesn't that mean that its working though? I'm so intolerant to feeling worse, I don't know how people go through worse herxes than this. You all are brave!
I have symptoms that could be something worse about every day. Lyme has given me the absolute worst health anxiety. I go through spans where I am in the ER about once a month because the nurse line told me that I could have something awful and need to go right away. Its always nothing. Its to the point that I am embarrassed to go.
I was just there about a week ago for pain over my liver that was spreading outwards. All they found was a UTI that wasn't symptomatic, but they treated it anyway. Before that was about a month ago because I was having stoke like symptoms, and was urged to go in. They said it was just a headache.
My concerning symptoms this time are my left foot keeps getting pitting edema every day, but a podiatrist says that is from tendonitis/beginning arthritis in my foot. I've never seen tendonitis or arthritis cause pitting edema, so I am having a hard time believing him, but I'm trying. I was rubbing that ankle the other night and found a lump just above the ankle. Its about the size of a long grape, and not present on the other side. It is right along the painful tendon. I made the mistake of googling about it, and DVT came up, and there is a vein that passes that spot. I think that is what has caused all of this anxiety about blood clots. The rest of my symptoms are easily attributable to lyme/anxiety (intermittent shortness of breath, dizziness, pains and soreness up and down my legs), I'm just always so scared it was something that was missed.
I really dont have anyone to talk to who understands. My husband tries to be understanding, but he doesn't get it at all. He thinks that I am not as sick as I think I am, and if I were to follow the instructions of my PCP I would feel better...Well, my PCP only thinks I have fibromyalgia, and she wants to prescribe gabapentin or lyrica. I don't think that will get me anywhere. My friends are slowly disappearing. They might ask me how I am doing occasionally, but if I tell them the truth they give me very short answers, or don't respond at all. I'm trying to believe they care, but it is hard to remember that.