The long wait for a diagnosis
Posted: Mon Nov 12, 2012 6:30 pm
Hello, My name is Amanda and this is my first time posting here. I have not been diagnosed with MS, however I am seeing a neurologist and I have had MRI's of my brain and spine done last week. My follow-up with the neurologist isn't until December 20th and the stress of not knowing seems to be making my symptoms worse.
I have already been diagnosed with stage 1 endometriosis 7 years ago and I was diagnosed with migraines when I was 11 years old. Last January I started limping for no apparent reason, I was feeling pain in my right hip and it felt like my right leg would just give out on me. Then after a couple weeks of limping I slipped on ice and injured my back. Since then my back has been a constant issue and then other symptoms started to creep up. I would feel "bee stings" and a burning tingling sensation at different parts of my body, I am always so tired and in pain somewhere in my body and if I overheat in a bath or shower I feel very ill. Lately I've been getting spasms, cramping, and shaky muscles. I am a 30 year old divorced single mother of 2 ages 6 and 3 and the complete degradation of my health and ability to do things with my children really started to get to me and I finally went to my family doctor. My family doctor said it was stress and put me on an anti-depressant called cipralex. I was on that for a few months when my doctor finally sent me to see a neurologist who right away changed me from the cipralex to Elavil(amitriptyline) and ordered the MRI's.
I hate being in limbo not knowing what is going on but my gut is telling me it is MS even though I hope it is not. Is there any advice anyone can give me from when they were going through the long wait for answers. I am scared and stressing about this and it's making my symptoms worse but I don't know how to not stress over something so scary.
I have already been diagnosed with stage 1 endometriosis 7 years ago and I was diagnosed with migraines when I was 11 years old. Last January I started limping for no apparent reason, I was feeling pain in my right hip and it felt like my right leg would just give out on me. Then after a couple weeks of limping I slipped on ice and injured my back. Since then my back has been a constant issue and then other symptoms started to creep up. I would feel "bee stings" and a burning tingling sensation at different parts of my body, I am always so tired and in pain somewhere in my body and if I overheat in a bath or shower I feel very ill. Lately I've been getting spasms, cramping, and shaky muscles. I am a 30 year old divorced single mother of 2 ages 6 and 3 and the complete degradation of my health and ability to do things with my children really started to get to me and I finally went to my family doctor. My family doctor said it was stress and put me on an anti-depressant called cipralex. I was on that for a few months when my doctor finally sent me to see a neurologist who right away changed me from the cipralex to Elavil(amitriptyline) and ordered the MRI's.
I hate being in limbo not knowing what is going on but my gut is telling me it is MS even though I hope it is not. Is there any advice anyone can give me from when they were going through the long wait for answers. I am scared and stressing about this and it's making my symptoms worse but I don't know how to not stress over something so scary.