Lyndsey
Active member
- Joined
- Dec 18, 2014
- Messages
- 89
- Reason
- DX FIBRO
- Diagnosis
- 04/2014
- Country
- CA
- State
- British Columbia
Hi guys,
I am on long term disability right now, but my human resource department at work also does follow ups with me on a monthly basis. Does anyone else deal with this or suffer from anxiety as a result? I find it so stressful to be asked about my expected return to work date, or if I have an idea. I have told my work a few times respectfully that i really don't know what to say as my symptoms only seem to be progressing and becoming worse. I am scared of the future and don't even know if I will be able to continue in the current field I am employed in. I constantly feel bad that I am off (as I have said in other posts sorry guys) and my husband always says not to feel bad as I have paid into disability and it is there for a reason. Even on my good days which are so rare, I feel guilty on those days. God, I wish I could just get over that feeling. Like others have said in the past to me in posts. I just find it helpful to come here and vent and hear others opinions and support, even if i am asking the same questions. At nighttime, which is the worst for me, I don't know who to talk to or where to turn so this is where I inevitably end up.
I am wondering if anyone else experiences the anxiety that I do over the illness itself and other things as well. The sleepless nights, insomnia, heart palpitations, nightmares, pain, and on and on.
so as time goes on I seem to find myself with new and worse symptoms...My worst symptoms are the chronic migraine and body pain. Lately I am having some serious stomach issues. Always having to use the washroom after I eat and having an upset stomach, throbbing in my joints, particularly my knees, shoulders and hips. Hips are the worst! Anyone else get this throbbing pain and or the IBS feeling? Sometimes my husband is like "really? something else". Honestly its so hard at times to explain to him and others. I know even myself i think half the time really something else!
Then I find myself wondering is this just going to continue to get worse and worse over time as it has for the past few years. The anxiety I have it very bad cant sleep at night and find that I am so anxious i don't even want to go to my bedroom cause i know i wont sleep. Such a vicious cycle. With also being diagnosed with PTSD, I wonder what came first the fibro or the PTSD. Are these two things actually related? I find it all so confusing.
Anyways, thanks to whoever takes the time to read my rant.
Thoughts and prayers with you all tonight, and thanks for your ongoing support and comfort. Hope I can also be there for you all when needed.
Lynds
I am on long term disability right now, but my human resource department at work also does follow ups with me on a monthly basis. Does anyone else deal with this or suffer from anxiety as a result? I find it so stressful to be asked about my expected return to work date, or if I have an idea. I have told my work a few times respectfully that i really don't know what to say as my symptoms only seem to be progressing and becoming worse. I am scared of the future and don't even know if I will be able to continue in the current field I am employed in. I constantly feel bad that I am off (as I have said in other posts sorry guys) and my husband always says not to feel bad as I have paid into disability and it is there for a reason. Even on my good days which are so rare, I feel guilty on those days. God, I wish I could just get over that feeling. Like others have said in the past to me in posts. I just find it helpful to come here and vent and hear others opinions and support, even if i am asking the same questions. At nighttime, which is the worst for me, I don't know who to talk to or where to turn so this is where I inevitably end up.
I am wondering if anyone else experiences the anxiety that I do over the illness itself and other things as well. The sleepless nights, insomnia, heart palpitations, nightmares, pain, and on and on.
so as time goes on I seem to find myself with new and worse symptoms...My worst symptoms are the chronic migraine and body pain. Lately I am having some serious stomach issues. Always having to use the washroom after I eat and having an upset stomach, throbbing in my joints, particularly my knees, shoulders and hips. Hips are the worst! Anyone else get this throbbing pain and or the IBS feeling? Sometimes my husband is like "really? something else". Honestly its so hard at times to explain to him and others. I know even myself i think half the time really something else!
Then I find myself wondering is this just going to continue to get worse and worse over time as it has for the past few years. The anxiety I have it very bad cant sleep at night and find that I am so anxious i don't even want to go to my bedroom cause i know i wont sleep. Such a vicious cycle. With also being diagnosed with PTSD, I wonder what came first the fibro or the PTSD. Are these two things actually related? I find it all so confusing.
Anyways, thanks to whoever takes the time to read my rant.
Thoughts and prayers with you all tonight, and thanks for your ongoing support and comfort. Hope I can also be there for you all when needed.
Lynds