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View Full Version : My Story -Large B-Cell Diffuse Lymphoma Survivor


TerryFord
08-03-2003, 05:48 PM
Let me start out by saying that I am(so Far) a survivor of this disease.

I am posting my story in the hopes that others may learn from my experiences.

This post may be a little long for some readers, but for others it may not contain enough info, if anyone needs more info please contact me and I will give as much info as I can.

My story begins in February of 2001.

I was very ill for approx. 6mos. prior to my diagnosis. My family doctor kept prescribing antibiotics for what appeared to be a combination of ear and sinus infections.

After the 3rd month(April) of these symptoms I had lost most of the hearing in my right ear. My doctor said it due to fluid build-up in my "Infected" right ear and that I should take these antibiotics until I could be seen by a specialist. The "ENT" (Ear-Nose-Throat) doctor had a waiting list and I would not be able to be seen until the first week of June. He was the only specialist in my area and the only one within a reasonable distance which was part of "My Allowed" network of doctors covered by my "HMO". The next couple of months was very bad, Sinus headaches, runny nose, coughing, etc. -seemed like the same old sinus infection problem. I dealt with it.
When I was finally able to see the "ENT" in June, he said that my throat looked very bad and put me on another antibiotic, aka "LAST CHANCE ANTIBIOTIC", and report back to him in 2 weeks, if the problem with my hearing was still there, he would place a tube in my ear to drain the liquid.

In 2 weeks I returned only to have him ask me to come back 2 days later to have the tube placed into my ear.

I did, my hearing returned as soon as the procedure had been performed...I was very happy and left.
2 days later I started having pain in the joint of my jaw, just below my right ear and a "SPLITTING" headache. I called the "ENT", he asked me to come and see him that day fearing complications from the "TUBE" procedure that had been performed.
After being examined, he said everything was fine and speculated that maybe I was suffering from "TMJ" which is a problem in your jaw-joint caused by "GRINDING" your teeth while you sleep, I disagreed with him, but he assurred me that everything was fine with my ear and if I should continue to have these problems I should again see my family doctor for a referral to another specialist for this problem.

After only a few days my sinus problem became worse and I again went back to my family doctor. He claimed I was again suffering from another sinus infection and tried to prescribe antibiotics again -I refused and expressed my concern about this sinus problem that we were unable to clear up with antibiotics. After realizing that I had been on many kinds of antibiotics since February, he agreed that there was indeed a problem and then asked me if I had ever been checked for allergies. I had not, so he was going to try to get me an appointment to see an allergist and sent me home.
The next day I awoke with a headache which increased in intensity over the next few days and I finally went to the emergency room. After telling them the story, they did an "X-Ray" and found my sinuses to be "VERY" cloudy. Told me to take tylenol and to see my family doctor ASAP. This was on a Sat. Evening, I had to wait until Monday to call my doctor.
On Monday I called my Doctor he asked me to come in, I did. I told him what was going on and also told him that in addition to the headache, I was also having a "Burning" pain on the right-side of my face, where the corner of my nose meets my lip. He asked some family medical history questions and after learning that my younger sister had "MS", thought that maybe I too was postitve for this and wanted me to go for an "MRI", I agreed and had it setup 2 days later.

My headache only intensified, I couldn't work, I couldn't function, everything I did only increased the pain in my head, I could only sleep for a couple of hours at a time due to the pain and none of the over the counter medication would get rid of it.
It was now the middle of August 2001.

I went for the "MRI"...it took 2 days for the results to get back to my doctor. He called me to come in and told me that my "MRI" looked very bad...it showed a huge mass in my sinuses...he again referred me to see the same "ENT".
I was supposed to see the "ENT" 3days later, this was the soonest he could see me.
The day before I was to see him my nose started bleeding, not out of my nose, but into my throat.
We called the "ENT" and told him what was happening...he asked if we could drive to the city he was working in that day and he would see me.
We went to see him and he "FINALLY" used a scope device which he put into my nose and had the first look at my tumor. He told us (me and my wife) that this looked very bad and wanted me to go to his office the next day for a biopsy.
After taking the biopsy on a Tuesday, he said they should know something by Friday.
My headache had only been getting worse...I called on Friday, they still didn't have the results, said it would probably be Monday now.
On Saturday morning the pain was absolutly unbearable...my wife drove me 80 miles to the Cleveland Clinic in downtown Cleveland. We told them the story, they gave me some narcotics for the pain and asked me to return on Monday with the biopsy sample and "MRI".
We returned to Cleveland on Monday, they confirmed that I did indeed have Large B-Cell Lymphoma and took bone marrow samples from both sides of my pelvis.

Asked me to return the next day to start treatments.
They told me that my cancer was probably genetic...they speculated that the "GENE" which caused my lymphoma, was probably the same gene that caused my sister's "MS".

It was a very tough regime of treatments...Every 3 weeks I would drive to Cleveland for Chemotherapy, Biotherapy and a Spinal Injection. I did this for 4 months Till the end of December.
I started having daily radiation therapy in January which lasted for 6weeks.

My doctor explained that my cancer seemed to be localized...not in my lymph nodes, bones, or organs, but he thought it was best to treat my illness as though it was everywhere. I agreed.

So far, so good...I have to go for checkups every4 months which consist of bloodwork and a catscan.

To sum it up....
I went through many months of pain and suffering, taking for granted that my local doctors were top-notch and would take good care of me.
Only after my wife decided to take me to the Cleveland clinic did I finally start to get relief.
I went for about 6weeks with a headache so severe that I could not function, I was unable to sleep, eat, or move....all I could do was sit on a couch, propped up by pillows and moan and groan while my kids and wife worried over me.

I spent 10 months of my life fighting this illness andwas off work for 8months...it gave me alot of time to see the world in another way.
The experience has changed my life in many ways...here are a few:

1. I Don't take life for granted.
I used to put off chores and family time to work because I thought there would be plenty of time to catch up later.

2. I Don't waste my time
I don't let little things bother me...they are a waste of time...I spend my time doing things that mean something to me or somebody else.

3. I don't try to fool myself
Material things do not mean as much as you might think. This illness cost me a very good job, a nice home and financial security -all of the things that I was sure I had to have to be happy.
Remember this.....after our lives are done, nobody cares if you met your sales quotas every month for 2 years, or confronted the neighbor about his dog messing in your yard....our "MAIN" job in life is to educate when we can and create memories for our kids and family whenever possible.
It is these memories that the people you leave behind will have for the rest of their lives....this will be your legacy!

Sorry so long...hope somebody has gotten something out of this.

Reply if you have questions or comments.

Thank-You,
Terry

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If You Always Do What You've Always Done, You'll Always get what you've always gotten.

[This message has been edited by moderator2 (edited 08-03-2003).]

wannabthin2004
08-04-2003, 02:26 AM
I'm so happy to hear your going to be ok. After reading your post I do have some questions. My oldest daughter, 7, last yr. the dr. ran some tests thinking she might have this lymphomia (sp)because her lymph nodes where staying large. Praise god it came out to be fine but after antibotic after another, they finally went down. She got her tonsils out and seems to be doing much better. But now i'm worried about my 5 yr. old. She has had so many ear and sinus infections and strap throat. They put tubes in her ears and adnoids out. That seem to help at first. Except for the constant drainage still. But she has repeatedly strap throat. One morn. she woke up and i swear it looked like she swallowed a grapefruit right on her lymph node. I took her immediatly to the dr. and it worried them. They gave her several shots and sent her to ent specialist. The shots helped but the ent says she fine now. She hasn't had strap throat in a while but i've noticed her lymph nodes are bulging a bit again but her throat is fine. What should i do?

SassyCat
08-04-2003, 09:22 PM
I to have been fighting lymphoma for 17 years. It keep's coming back. In Dec. I was in critical care for 5 days & in the hospital 12 days. Then I went to a nursing hhhhhhhome to get my strength back.I am 66 years old. I'm having a cat scan on Thur.to see if it went to my lung's. I have been coughing for about 4 month's. ......i am scared. Please pray for me.
SassyCat

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TerryFord
08-05-2003, 02:27 AM
Hi Folks!

WannaBeThin....I can only say this...
I am by no means an expert on this, but I would seek other opinions...as in my story, I was certain that my doctor knew best, I followed his advice and eventually I found that he and his office missed the diagnosis.

Remember, they are the professionals and it quite possibly could be nothing to worry about.

If you live in a small town as I did, I would go to a bigger city's medical facility....they have more resources to use to find you an answer quicker.

The Doctor I was seeing for my illness told me that I was "VERY" lucky that my tumor was caught early.
He told me that most people with lymphoma in their lymphnodes do not notice any symptoms until the disease has started to spread and that is much worse.

The location of my tumor was in my sinuses and with the growth of the tumor it caused severe pain because it had nowhere left to grow. Thus we were alerted to it sooner than most.

I have 5 boys and 2 girls ranging in age from 16 down to 6.

I hope this all works out for you...I can't imagine one of my children having to go through similar testing and treatments...it would crush me.
I wish you the best!

 
 
 




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