Why are some healty & others of us, suffer so much?
December 9, 2008 10:21am
Dear Journal,
It has been a while. I suffer thru not only with my own pain everyday, but, watch my youngest daughter in all her …
Progress
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cynthiak777
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About Me
cynthiak777
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About Me
I have hep c, migraines, fm, chronic fatigue, back aches from herniated disc, a shoulder that burns after (30) minutes of sitting anywhere, high blood pressure and fighting severe depression daily
I have hep c, migraines, fm, chronic fatigue, back aches from herniated disc, a shoulder that burns after (30) minutes of sitting anywhere, high blood pressure and fighting severe depression daily
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Interests
I love to do crafts, especially during the holidays, wreaths, ceramics, etc. playing with my grandkids, collecting shells, reading good books, and listening to all kinds of music, religious, Indian ((I am Cherokee) Enigma, country, and oldies, that is my peace!
I love to do crafts, especially during the holidays, wreaths, ceramics, etc. playing with my grandkids,
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Recent Activity
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Journal
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My broken Heart
October 5, 2008 9:53am
Dear Journal,
I have stayed in the other room, in my own world of pain, to avoid confrontations, only to be attacked as soon as he wakes up …
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It hurts to be the good guy
September 28, 2008 2:59pm
I have spent my entire life being good to others, always going the extra mile, forgiving when they repeatedly broke my heart, used me, or lied and …
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Today could be a good day
June 2, 2008 4:45pm
The day started out as always, in pain, but, I pushed thru it, listened to God, who told me not to take any pain meds till I absolutely had to, which …
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Journal Entry for May 24, 2008
May 24, 2008 10:31am
DEAR JOURNAL,
I finally have found a support group, so I will not feel so alone. After raising (9) children, and half of my (23) …
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Hugbook
Prayer
Thank you for making your daughter aware that people do care and we are all in this together. I have no treatment at this time, my doctor and I are hoping that it is the blood pressure that is causing the most of my problems. I don't need to take shots but I'm sure some day I may need to. My leggs not only freaze up but at times I can hardly even get out of bed. It takes our dog lilly and sometimes anthony to get me out of bed. I have found that the cats are licking my feet often which I hate but it brings a feeling back into them. I will email your daughter and let her know that she is welcome to join us here at DS and that even if she just needs a friend to share her day I will be around. God bless you all.
Hug
Hello, I am sorry to read that your daughter has MS. I was diagnosed over a year ago. I waited till a few months back to start on copaxon. Side effects I deal with while on Copaxon is the area I did the shot it gets puffy and red, itches. One thing I do want to recommend you daughter not doing is doing the injections in her stomach. I have done the injections at the most 5 months and the tummy is all lumpy. The arms can get that way too, but hasnt with me. Tell your daughter next year as long as the FDA doesnt screw us the pill form for MS will come out. It is nice meeting you, write me when you want to talk
Prayer
I am so sorry your daughter is going through this. I have no firm dx yet and very frustrated. I have days where I feel normal and days where I just am a mess! I am so sorry that your daughter has been hit so hard by this. I saw a guy on here the same thing happened to him...just a big WHAM and he was really sick in a big hurry. My symptoms have been off and on since 2004-the 2004 bout was one of the worst along with this last one. I just had an MRI done so we'll see if it shows any lesions...doubt it. I have had vertigo, balance issues, urine problems, joint pain, numbness/tingling with patches in certain places of my body worse than others. My right knee is partially dislocated-so that hurts all by itself. I am beginning to lose hope that I will get someone to help me. I think I am going to go to St. Louis or Chicago to big med center where they might be able to nail it down more. I am going to see a genetics dr. in summer so I am waiting for that before I proceed on (if I even have to). The genetic dr. might be able to help me. I am adopted and have no history to go off of from my birth family. It sure would make things easier if I did! I want to look them up but I just don't have the drive/strength to do so. It might be worth it though. I know MS can't be dx through a blood test or anything but the genetic dr. might be able to shed some light on it and possibly look at marfan and ehlers danlos for which I fit the profile for as well. My son has traits as well. So, what are they doing for your daughter? Is she part of this site? I would encourage her to join if she has not already. It really helps to talk to others in the same boat. Bless you and your daughter and your family are in my prayers. Jennifer
Kiss
Louise Hay, You Can Heal Your Life. The book, the audio CD, the movie. The answers. You are whole, perfect and complete.
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Ray of Sunshine
Many bright blessings, dear sister, hoping that things get better for you. You deserve to be healthy and happy!
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Photos
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Support Groups
Close Hepatitis C
I have hep c, fm, cfs, and (9) different kinds of headaches, as well as high blood pressure. I live on the beach, which the scenery and feeling closer to God helps me, but, I have had to give up my career and stay at home, driving me nuts, need companionship! Update, I am going back to work, tomorrow, brand new field, wish me luck! Who else feels like a mac truck hits them daily and worse with the pegintron shots?
Close Multiple Sclerosis (MS)
Type: Relapsing-remitting MSMy daughter was diagnosed with MS about (2) months ago. She is going thru Hell, lost 97% of her vision in her right eye, in constant pain, legs, back & Head, in flare up, on Copaxone now, steriods, and a host of other meds. This is greek to us both, trying to learn what can help, and what to expect, she could use some friends that have been going thru it for a while, that can love & support her & visa-versa. She has also, had (9) surguries, female, gall bladder.
Treatments
- Copaxone Too Soon to Tell
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Groups
