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A changing life

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Lyme Disease
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Biggs
Regular Member
Joined : Aug 2012
Posts : 23
Posted 8/27/2012 1:30 PM (GMT -8)
I just can't stop crying! Just came from Lyme specialist and now she started me on a new abx for what she suspects bartonella she explained when you have it so long it hides. But if I herx with the new med then she will treat me for it. I start a three month iv protocol. I was aiming to go back to school in November (I teach) but the last three days I've been in bed. My life is changing big time I sure as all of yours, but today I can't get a grip. I cant work, I use to chair up the ACS Relay- no more, even my social life has come to a screeching halt. I think my friends are sick of being around the sick girl (they carried me through cancer, probably had enough!) we cancel invites, we don't entertain, no the financial stresses. I feel this is no fair to my husband. I'm just dying a slow agonizing death, ever feel that way? I'm in such a bad place, just tired of it all
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springsjean
Veteran Member
Joined : Mar 2009
Posts : 2185
Posted 8/27/2012 1:57 PM (GMT -8)
OMG I feel so bad for you. But please know that it will get better. you have been so much so make sure you pamper yourself but don't blame yourself. It is not easy but we all have challenges that we face and getting thru them make the good days even better.

Bartonella can be very hard on your nerves and anxiety. Be sure to take some deep breathing sessions (Iknow sounds crazy but got me through some pretty bad times), some naps, mind escapes like movies or reading or crafts, and healthy eating and detoxing with lemon water.

It takes much patience and positive thinking and I never thought I would get there but life takes on such new meaning when you get through such a setback like lyme.

I hope we can be of help to you. A good crying session does you well as long as you pick yourself up and move on with determination. Hope today gets better for you. Feel free to vent and message at any time.
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achievinggrace
Veteran Member
Joined : Nov 2009
Posts : 3266
Posted 8/27/2012 4:00 PM (GMT -8)
Ahhh, Biggs,

Some days the mountain is just too hard to climb. You can't see the top, you don't care for the cold, and you don't remember signing on for this in the first place!!

Yes, we have all had days like you are having. Maybe we have let ourselves go even longer than that, on occasion! No, it isn't fair, most of all to our helpmates and other family. But this is the hand we have been dealt.

The good news is that you have treatment available to you; multiple kinds, even. You have coped with cancer, good for you -- you can do this, too. You probably won't get so much as a stinking casserole out of this one, though. Even the most compassionate of your friends isn't going to get this. That's okay, those casseroles are a bit dodgy, aren't they?! I mean putting your whole dinner in one dish doesn't make it better, does it?

You will get better, in fact, you will be fine. Try not to worry -- I know, it's hard, when every nerve is screaming. Hey, we are here for you. Keep talking!
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Willowrose
Veteran Member
Joined : Oct 2009
Posts : 699
Posted 8/27/2012 4:14 PM (GMT -8)
Hi. So sorry you are going through this. Oh yes, I have felt and do feel that way. One of the most difficult things to manage for me has been the sense of loss. I gave up my teaching job, strenuous hobbies, and many friends who just didn't understand. I've lost the sense of well being, I'm tired of hurting, I'm tired of new maladies cropping up just as others subside, sometimes I'm even tired of trying to get better. With this cluster of infections, a person has every justification to cry and feel down. But I can't stay there for long because it's not productive and as long as I'm living I'm going to make my life the best I can from where I am, if not for me then for the people who love me. Wishing it was different just doesn't get me anywhere positive.

Slowly over time I've replaced teaching with substituting so I can choose what days I'm able to work, found less strenuous hobbies (substituted sewing, learning an instrument and walking for hiking, rock scrabbling, and being a gym rat), and found lyme friends and others who are more understanding. These days I go ahead and make commitments and usually I can make it. When I can't, I don't. I encourage the rest of my family to still go and when they will, I use the alone time to regroup. I've found it works best for me to proceed as if I will be well and then make adjustments if I'm not.

Every day begins with a pep talk to myself. Throughout the day there is a perpetual redirection of negative thoughts to counting my blessings. Maybe it's the Bartonella, but I tend to get stuck in negative loops of thought that seem so real when I'm thinking them; later or the next day I wonder how I ever thought that way. It's almost like an eclipse of reality. I'm learning to recognize when I'm stuck like that and I tell myself it isn't real and it will change soon. That can help. And, as much as it goes against my natural inclinations, I work to be kind to myself. Sometimes that includes crying for the loss of my health and everything that's associated with it. When I'm finished, I fix a cup of tea (drinking one now) and sit quietly focusing on something beautiful until I feel calm inside again.

I hope by now you are already exiting the bad place you've been in and are seeing the world with refreshed eyes.

Rose
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Biggs
Regular Member
Joined : Aug 2012
Posts : 23
Posted 8/27/2012 4:40 PM (GMT -8)
All your words are so kind and insightful. I'm the one that usually gives the pep talks but not today. I've been working on self care and kindness. I've always been active and wouldn't miss a party. I no longer recognize myself. I keep telling myself I just need to redefine my life. I think what hurts the most I feel my so called friends left me in the dust. I just couldn't keep up. And the fact I can't teach at this time. Does it really get better or are they just kind words we share.
I loved the comment about the casserole , that is so true. I think
People think I make all this crap up. There's to much to be making this stuff up. I think I need a good nights sleep and tomorrow will be better. Thanks for the much needed support.
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borderlyme
Veteran Member
Joined : Jul 2011
Posts : 1486
Posted 8/27/2012 6:40 PM (GMT -8)
It is really painful when we feel abandoned by our friends, but it really does show you who your true friends are. What helped me a lot in dealing with losing relationships was reminding myself over and over again that it isn't personal. I don't hate my old friends for not wanting to maintain the relationship - I just try to appreciate them for who and what they are and if I can mantain a casual, acquantaince-type relationship with them, great, if not - there are ALWAYS new people to meet! Who knows, maybe the universe wants you to go through a purging like this! It's no one's fault - I don't intend to be a "bad" friend, I just happen to be unable to follow through with plans. They don't mean to be bad friends either, it just is what it is.

Sometimes it all hits so hard - with so much at once, it's really hard to process it all and still feel confident that everything will be okay, and it will. You may come out of this feeling much better than you ever did before, I know that's how I feel, though it wasn't always easy! Hang in there - we're here for you!
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TICKLEDPINK
Veteran Member
Joined : Jul 2012
Posts : 914
Posted 8/27/2012 10:55 PM (GMT -8)
Hi there,
what wise words from the forum members!
I have found that my feelings of guilt tend to paralyse me,I feel guilty for neglecting my friends,not being able to do my chores properly and being too tired to take my darling dogs for long walks......the list goes on and on.
These feelings cause me to cramp up and I spiral into more pain,it's a very vicious circle.
I do try to pull myself together and accept that it isn't my fault-I'm very ill and in pain but sometimes it's just too overwhelming.
We have to learn to take strength from the OK days and persevere through the bad ones.

Diana
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Deejavu
Veteran Member
Joined : Aug 2005
Posts : 4771
Posted 8/28/2012 3:53 AM (GMT -8)
Hi Biggs,

Your words bring back the pain I felt when I was sick...  No wonder the words that Robin Williams said to Matt Damon in the movie "Good Will Hunting" made me cry so much... "It's not your fault, it's not your fault".... 

And yes, you received very wise thoughts from the other members.  I really found out who my "real" friends were... It's nuts that cancer is "acceptable" but lyme disease is still a mystery to most people... They don't get it unless they "get it"...  I used to tell people when I was sick that I was going to find ticks and hide them in a room so people who didn't have lyme would get bit!  Of course I never did that but hey, I'm nuts!  Always was and always will be...  And you know what?  I like myself that way... I don't care what other's think....

What matters most is what I think and that I like myself...  I think that came with age...  When I was younger I DID care what others thought of me...

Anyway, my marriage broke up because of lyme.  I was not married that long and I was very much in love and I believe my husband back then was very much in love with me.  He knew me as a person who worked at least 10 hours a day, could clean the house, cook fantastic meals, and had lots of energy afterward...

When I became sick (I was undiagnosed for 5 long years), he couldn't handle it.  So he was not nice to me because he was expecting dinner on the table and that dinner stopped being there.  He expected a clean house only to find a dirty house.   He wondered where I went... I couldn't give him any answers as I didn't know what was wrong with me either..  I went from doctor to doctor to doctor...  No one could tell me anything..

We ended up fighting so much.. I couldn't take the stress (good thing we didn't have kids)..  I asked him to move out so I could have peace and quiet..  Eventually he did and later on we divorced... 

Talk about being alone... I was totally alone (my family never head of lyme either and they were NOT supportive)...  So I was grateful for my 2 doggies back then...   I finally had unconditional love...  My 2 dogs were my support system...  5 years later when I was finally diagnosed with lyme I joined a support forum..   And then I got well... 

Golly, I didn't mean to write this much... 

Biggs, hang in there... Do things alone with your husband if you feel well enough..  Read poetry to each other..  Give each other massages...  Light candles and turn off the lights and put on music... 

Things will get better... If they could get better for me which they did, they can get better for you too... 

Hugs to you,

Denise

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Biggs
Regular Member
Joined : Aug 2012
Posts : 23
Posted 8/28/2012 4:59 AM (GMT -8)
Thx Denise, I'm sorry you had gone through all that. My heart breaks when I hear how so many of us suffer in silence for so long. It frustrates me that the medical profession does not open up their eyes to this epidemic! And how people look at you like you have a third eye. It's not a disease that is visible unless you have the muscle and joint problems, then I remembered being teased about being a little old woman!!!! I remember last year a few of my close friends, so I thought, would tell me stories how they knew of someone who had lymes and never missed a day a work. My response was lucky them!!! As soon As I started my doxy and Mino I felt a bus ran over me, at that point I had to take a leave of absense. I was sickly for at least 8 years and as soon as I start abx everything gets 10x worse. I couldn't understand it, and neither could others. Now I know how it works, but some friendship bridges were burned. As far as my husband, he should receive a gold trophy. He stuck by me thru three long years of cancer stuff, we had a year break then this. Actually it was the cancer that helped get the lymes diagnosed. He is still at my side and waits on me and is my pillar of strength and hope. I'm afraid he's going to wake up and say this is not what I signed up for. This has taken such a toll on us financially (between the cancer and this back to back). That's what scares me. So I blabed about everything under the sun! Those of you that read this thanks, I have just joined the forum days ago and already I don't feel quite so lonely and crazy! May all of you have the best day possible! I know we choose our outlook- today is sunnier than yesterday!
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flowergal
Regular Member
Joined : Sep 2011
Posts : 464
Posted 8/28/2012 4:05 PM (GMT -8)
Biggs,

The people on this forum are a life line to me and will be to you too. They understand as I do, all that you are going through. My husband too has been supportive giving up his Saturdays to drive me out of state to the Doctors. We try to make it a mellow "date" and go out to eat after the appointment. In the early days I did not talk much on those trips as I was too out of it, but it does get better. Also the abx can make you feel worse in the beginning at least that is what happened to me.

As for friends for whatever reason there were lots of weddings and showers this summer I only made one. Anyone who knew me before knows I would not miss a social gathering but now I find I have to explain myself. On the positive side my husband doesn't like those events and was happy we could not go! He is also happy I am back to being the skinny girl he fell for a long time ago...I didn't care about losing weight, it was my mind I didn't want to lose!

Anyway use this forum to vent, or email someone when you need to "chat". I and others will support you just as we were supported.
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AndyD81
Regular Member
Joined : Aug 2012
Posts : 25
Posted 8/28/2012 5:01 PM (GMT -8)
Hang in there Biggs. It gets better. You will have your health and your life back soon, just keep strong.
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beachlover89
Regular Member
Joined : Nov 2011
Posts : 265
Posted 8/29/2012 7:40 AM (GMT -8)
So sorry...I too grieve over the life I had..but when I get in that place...I pray and God always answer my prayers! :-)
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