Living with lupus

My participation in the discussions on this website has provided some very revealing thoughts and feelings of those suffering from lupus and associated diseases.

The healthy release of your emotions, coupled with details of your fight against this formidable foe, have engendered a greater compassion for those afflicted with these cruel conditions. I share many of your concerns as I struggled with lupus, interstitial lung disease and bipolar disorder.

With that in mind, here are some observations to ponder:

*** The rollercoaster ride of pain and relief: The pain brought by the list of numerous symptoms, which can come and go for no apparent reason, seem never-ending. But then there are the brief periods of improvement. They offer a glimpse of hope for the future, only to most often be shattered by a return to the prevailing symptoms that so baffle our doctors.

The worsening side effects of various medicines and the fear of the long-term impact of prednisone and other meds don't make the task of coping any easier. Everyone needs to sense a "light at the end of the tunnel," a feeling that a cure might eventually be in the works.

It doesn't help when we sometimes must deal with doctors whose approach appears to be one in which they only 'cover providing only what they feel is required of them at the time, refusing to consider other options, such as new drugs or combinations of such, that might improve a patient's condition.

**Overpowering Depression: All of this negativity can lead to an overwhelming feeling of depression, a frightening state of mind in which the patient sees only increased misery on the horizon. There are feelings of abandonment, resentment and self pity to deal with. Who really cares about me? Who are my true friends? Who can I count on?

Some combat the Illnesses better than others, perhaps due to a more optimistic nature or good news from good doctors. Some continue with the downward spiral, unable to overcome what they anticipate to be only further misery.

**Coping: So how do we deal with this as life unwinds? Coping mechanisms are many, including this well-intended website that allows people to vent frustrations daily. Unlocking of one's emotions is often a good thing. Everyone's approach is different, with the obvious hoped-for outcome of finding a way to function each day and remain as independent, healthy and happy as possible.

I recommend a "bucket list" for those still hoping to enjoy life. Take the time to rediscover the enjoyment of old hobbies that can help occupy time in a fun way. While maintaining a reasonable assessment of one's physical limitations,I feel we should strive to experience some activities we always envisioned as fun but for whatever reason never attempted. This could be something as radical as skydiving or simply traveling to a location you always wanted to see (mine would be ALaska's Kanai Peninsula for fishing). Watching movies redolent of a more cherished time can also be therapeutic for me. It can take you back to happier times.

At any rate, always remember to never give up. There is always hope.

Thomas Franklin

Beautifully spoken.... yes there is always hope.

Thank you. Hope it helps in a small way.

hopeful said:

Beautifully spoken.... yes there is always hope.

You are so right. Even though there are times when our brains and bodies won't admit it, there is hope. We have to try and find a glimmer of it, even just flashing by for a short second. We never know for certain what the future holds for us. That is the truth. So, it is logical to have hope, not only logical but healthy and healing.

Thomas, that was fabulous! So eloquent. May I share ur letter on my Facebook page? It really shows those on the edges of lupus(family/friends) what it looks like from inside. I will,of course, give u credit!

Of course you can. I would be honored. Thanks.

Thomas

Kari said:

Thomas, that was fabulous! So eloquent. May I share ur letter on my Facebook page? It really shows those on the edges of lupus(family/friends) what it looks like from inside. I will,of course, give u credit!

Thank you…you are inspiring. …god bless…

Thanks Thomas for putting the words together well. I find it difficult a lot of the time to put into intelligent words what I'm going through/feeling when I am dealing with Lupus and it's complications. Be well Thomas.

Patrick

Thank you so much for the beautifully written sentiment. I saw a wonderful movie this weekend called "The Giver" from the children's book. We are lucky to still have choices in our lives and we are not doomed, we just have to keep trying.

You have inspired me to draw and paint again!!

You honor us all!

Thank you for sharing!

Thank you! this is what I needed. I don' always necessarily feel hopeless as much as misunderstood. Those around me don't "get it" So I put on a fake smile and wear myself out to keep up. Then sit at home and cry because the pain is excruciating....

I love the idea of the "bucket list" And am actually ticking one off this weekend.. I am in AZ from PA visiting my daughter for the birth of my first grandchild (another bucket list check) and we are going to San Diego. I've always wanted to dip my feet in the Pacific Ocean and now I get my chance....

Hello Thomas , this is so very true and beautifully worded /said . My kids read this and they were like wow!!! Thanks for speaking from the heart ,that really put light on it for those that REALLY don't know what we GO THROUGH Living with LUPUS every day .Thanks again , i Love this ...Beverly L.

Great! Sounds like fun. Enjoy.

Thomas

lorri64 said:

Thank you! this is what I needed. I don' always necessarily feel hopeless as much as misunderstood. Those around me don't "get it" So I put on a fake smile and wear myself out to keep up. Then sit at home and cry because the pain is excruciating....

I love the idea of the "bucket list" And am actually ticking one off this weekend.. I am in AZ from PA visiting my daughter for the birth of my first grandchild (another bucket list check) and we are going to San Diego. I've always wanted to dip my feet in the Pacific Ocean and now I get my chance....

Glad you liked it. Keep the faith and keep living life.

Thomas

Beverly L. said:

Hello Thomas , this is so very true and beautifully worded /said . My kids read this and they were like wow!!! Thanks for speaking from the heart ,that really put light on it for those that REALLY don't know what we GO THROUGH Living with LUPUS every day .Thanks again , i Love this ...Beverly L.

So true Alex

Alex said:

You are so right. Even though there are times when our brains and bodies won't admit it, there is hope. We have to try and find a glimmer of it, even just flashing by for a short second. We never know for certain what the future holds for us. That is the truth. So, it is logical to have hope, not only logical but healthy and healing.

Very well said!! Carry on.


You do the same !!! I really enjoyed this ....Beverly L.
Thomas Franklin said:

Glad you liked it. Keep the faith and keep living life.

Thomas

Beverly L. said:

Hello Thomas, this is so very true and beautifully worded /said. My kids read this and they were like wow!!! Thanks for speaking from the heart, that really put light on it for those that REALLY don't know what we GO THROUGH Living with LUPUS every day. Thanks again, i Love this... Beverly L.

Thank you for sharing this encouraging and inspiring words. Also thank you for the reminder that there is ALWAYS HOPE!! I have had a rough week and needed the reminder.

Hugs and blessings,

Stacey

Thomas, great discussion. What's next on your bucket list?